Journal of the American Academy of Dermatology
Volume 62, Issue 1 , Pages 13-28, January 2010

Caterpillars and moths:

Part II. Dermatologic manifestations of encounters with Lepidoptera

  • Eric W. Hossler, MD

      Affiliations

    • Corresponding Author InformationReprint requests: Eric W. Hossler, MD, Department of Dermatology, Geisinger Medical Center, 115 Woodbine Ln, Danville, PA 17822.

Article Outline

Caterpillars and moths (order Lepidoptera) are uncommonly recognized causes of adverse cutaneous reactions, such as localized stings, papular dermatitis, and urticarial wheals. These reactions are typically mild and self-limited; however, in South America, the sting of Lonomia caterpillars can cause a potentially fatal hemorrhagic diathesis related to massive fibrinolysis. In addition, ocular inflammation and prominent arthralgias have been reported to be caused by caterpillar exposures. Therapies for mucocutaneous reactions to Lepidoptera are largely empiric, with the exception of antivenin against Lonomia obliqua envenomation. Part II of this two-part series on caterpillars and moths reviews the varied symptoms caused by Lepidopteran exposures, reviews the differential diagnosis, and discusses appropriate treatment algorithms.

Learning objectives

After completing this learning activity, participants should be able to recognize the most common species that cause caterpillar- and moth-related reactions, categorize the reactions based on the clinical manifestations, and choose the most appropriate therapy.

Key words: dermatitis, insect bites and stings, Lepidoptera, moths, urticaria

 

Capsule Summary

 


The clinical patterns caused by caterpillars and moths are localized stinging reactions, papular urticaria and dermatitis, urticarial wheals, hemorrhagic diathesis, ophthalmia nodosa, dendrolimiasis and pararamose, bites, and oral exposure.

The differential diagnosis for these reactions is broad, and a history of caterpillar or moth exposure is helpful in making an appropriate diagnosis.

Treatments for these reactions remain empiric, but an effective antivenin exists for Lonomia obliqua stings.

Lepidoptera are one of the most diverse groups of insects, but they are an uncommon cause of human disease. Their effects on humans are as myriad as their diversity. In the first part of this two-part series, I defined the terminology related to caterpillar- and moth-related disease, reviewed the epidemiology of caterpillar and moth envenomation, and discussed known pathologic mechanisms of disease caused by these insects. Part II of this review will provide more clinical information on each clinical pattern of disease caused by Lepitoptera and provide information on the species of caterpillar or moth that is potentially responsible for each pattern. In this way, the reader may use either the clinical impression or correct identification of the offending species to guide both management and therapy. An overview of published therapies is provided at the end of this review.

Back to Article Outline

Symptoms 

Key points

Localized stinging reactions are caused primarily by caterpillars of three families: Saturniidae, Megalopygidae, and Limacodidae

Papular urticaria and dermatitis tend to be caused by contact with furry or bristly caterpillars

Urticarial wheals, angioedema, and anaphylaxis are most commonly reported with processionary caterpillars (genus Thaumetopoea)

A hemorrhagic diathesis can result from Lonomia stings

Moths with the ability to pierce human skin have been reported

Ophthalmia nodosa results from ocular contact with caterpillar setae

Dermatitis associated with prominent joint findings is reported with Dendrolimus and Premolis caterpillars

Oral exposure may occur in children and is usually mild

Cutaneous reactions to Lepidoptera come in many forms, most commonly mild stings with a papular eruption, pruritic urticarial papules and plaques, or scaly erythematous papules and plaques in exposed areas. Consequently, the differential diagnosis is often broad, and diagnosis requires a high index of suspicion and thorough history. Patients may provide a history of caterpillar or moth exposure, and a general knowledge of the most common offending species in that area can be of great help.

Accurately classifying human reactions to encounters with Lepidoptera is difficult because of poor documentation. There are only scant publications on the subject, and those that are available lack uniformity in either scope or investigation. The great diversity of offending species along with difficulty in accurate speciation adds to the problem. In tropical areas, where the diversity of Lepidoptera far exceeds that of temperate regions, Lepidoptera may be largely unclassified, and there may be a complete lack of documented medical records in these areas. A further difficulty is that some species are capable of producing myriad adverse effects: the caterpillars of the browntail moth (Euproctis chrysorrhea) are able to cause eczematous dermatitis, papular urticaria, urticarial wheals, vesicopustular eruptions, bruising, conjunctivitis, rhinitis, and possibly fatal allergic reactions.1, 2, 3, 4 Most species, however, primarily cause one type of reaction, and it is with this in mind that the following classification is offered: localized stings, papular urticaria or dermatitis, urticarial wheals, hemorrhagic diathesis, ophthalmia nodosa, prominent arthritis/arthralgias, bite reactions, and oral exposure (Table I).

Table I. Overview of Lepidopteran reactions
ReactionDescription
Localized stinging reactionsImmediate mild to severe pain that lasts hours to days; uncommonly associated with systemic symptoms
Papular urticaria and dermatitisMild to moderate localized pruritic papules or eczematous patches; predominantly exposed areas; may last for days
Urticarial whealsEvanescent pruritic wheals with or without angioedema or anaphylaxis
Hemorrhagic diathesis (Lonomism)Localized stinging reaction followed by headache, mucocutaneous hemorrhage, potentially fatal alveolar or cerebral hemorrhage, or renal failure
Ophthalmia nodosaAcute unilateral chemosis, occasional granulomatous inflammation or uveitis
Dendrolimiasis and pararamoseNonspecific dermatitis associated with prominent joint involvement (arthritis or arthralgias)
BitesRare; mild and self-limited
Oral exposureTypically mild and self-limited lip or oral mucosal irritation

The following paragraphs and tables are organized first by predominant symptom and then by geographic location to help clinicians with accurate diagnosis and speciation.

Localized stings 

In the United States, localized stinging reactions caused by caterpillars are largely due to members of three families: Saturniidae, Megalopygidae, and Limacodidae (Table II). The Saturniidae are known as silkmoths, and the strictly American subfamily Hemileucinae contains all the known stinging Saturniidae. Composed of 49 genera and approximately 670 species from Canada to Argentina and Chile,5 all species may be capable of stings, although the caterpillars of most species have yet to be described. Larvae of at least seven genera (Automeris,6, 7 Hemileuca,8 Leucanella, Molippa, Dirphia, Cerodirphia,9, 10, 11 and Hylesia12) are known to sting.

Table II. Some common caterpillars that cause localized stings
Common nameSpeciesLocation
Io mothAutomeris io6, 7Southern Canada, Eastern US to the Rocky Mountains, south to Costa Rica
Buck mothHemileuca maia8Eastern US
Palometa peluda (little hairy pigeon)Hylesia spp.5, 12, 56, 60, 136, 137, 138Mexico, Central, and South America
Cup mothDoratifera vulnerans, D oxleyi, and D quadriguttata38, 40Australia
Billygoat plum stinging caterpillarThosea penthima39Australia
Stinging nettle caterpillarDarna pallivitta18, 19Hawaii and Southeast Asia
Slug caterpillarLatoia (Parasa) lepida41, 42Japan
Puss caterpillar, flannel moth caterpillar, asp, bicho peludo negroMegalopyge opercularis and M crispata21, 22, 23, 24, 25, 26, 27, 28, 29, 30Southeastern US south to Central America
Gum leaf skeletonizerUraba lugens35, 36, 37, 38Australia and New Zealand
Mourning cloak (US), Camberwell beauty (UK)Nymphalis antiopa17, 47North America and Eurasia
Danaid eggflyHypolimnas misippus38Southeast Asia, Africa, tropical Americas, and Australia

UK, United Kingdom; US, United States.

The most well known member of the Hemileucinae is the io moth, Automeris io (Fig 1). It is commonly found throughout the summer from southern Canada throughout the eastern United States, and is also found as far south as Costa Rica.13 Contact with caterpillars causes a nettle-like stinging sensation followed by a pruritic papulourticarial eruption that may last for hours.7, 13 Dizziness, diaphoresis, and abdominal pain are rarely reported.14 The similar A louisiana can sting and is found nearly year round along the Gulf of Mexico in Louisiana, Mississippi, and Texas. Also belonging to this family is the buck moth, Hemileuca maia (Fig 2), which is commonly found in the eastern United States. It causes mild to moderate stings similar to that of the io moth.8 In the western United States, the closely related range caterpillar (H oliviae) may cause localized stings. There are 16 other species of Hemileuca in the United States and Canada, all of which possess stinging capability.15

In the family Limacodidae, the most well known caterpillar is the saddleback (Acharia stimulea; Fig 3), which is common throughout the eastern United States to Texas and Florida from late summer into October.13 The stings are potent; contact causes intense pain and urtication or vesiculation (Fig 4).16 Less intense stings are caused by other members of the Limacodidae found in the eastern United States: Natada nasoni, Parasa chloris, P indetermina, Euclea delphinii, Isa textula, and Adoneta spinuloides (Fig 5, Fig 6, Fig 7, Fig 8, Fig 9).17 In Hawaii, the stinging nettle moth (Darna pallivitta) was introduced in 2001 from Southeast Asia. Contact causes immediate stinging and wheal formation, which may take up to 5 days to resolve.18, 19

In the United States, the most severe stings belong to the caterpillar of the southern flannel moth Megalopyge opercularis (family Megalopygidae), commonly called the puss caterpillar. It is found in the eastern United States from the mid-Atlantic states through Texas into Mexico and central America throughout the summer but especially from September through October, when the highest numbers of stings are reported.20, 21, 22, 23 Caterpillars, also called “asps” or “bicho peludo negro,” are easily recognized by their wooly appearance and characteristic “tail” (Fig 10). There are spines hidden within the dense hair coat that cause severe burning pain, edema, erythema, and a characteristic grid-like hemorrhagic papular eruption (Fig 11).24, 25, 26, 27, 28, 29 Up to one-third of victims may have systemic reactions, including lymphadenopathy, headache, acute abdominal distress, muscle spasm, faintness, vertigo, respiratory distress, swallowing difficulty, shock-like symptoms, or convulsions.21, 22, 23, 28, 29, 30 A fascinating catalog of reported stings can be found at http://www.bugsinthenews.com/puss_caterpillar_encounters.htm.31 In the northeast United States, the similar black-waved flannel moth (M crispata) causes a less severe sting.26 Other Megalopyge species, including M urens, M lanata, and M krugi, found in Central and South America, may also be capable of severe stings.10, 32, 33 A related species, the white flannel moth (Norape ovina; Fig 12), causes mild stings and is found from Virginia to Missouri and across the southeastern United States.13, 34

  • View full-size image.
  • Fig 11. 

    Sting of puss caterpillar, with characteristic hemorrhagic “grid-like” appearance. (Photograph courtesy of Dirk M. Elston, MD, Geisinger Medical Center. Image is in the public domain.)

In Australia and New Zealand, the gum leaf skeletonizer moth (Uraba lugens; Fig 13) is another member of Limacodidae whose stings cause pain, erythema, and wheal formation (Fig 14).35, 36, 37, 38 Australia is the home of several other stinging Limacodids, including the billygoat plum stinging caterpillar (Thosea penthima), which can cause mild to severe stings, in one case associated with crushing chest pain.39 Members of the genera Doratifera,38, 40 Microleon, Monema, and Scopelodes17 also can cause human stings.

Reports from other continents are sparse. Two Asian Limacodids have been reported: in China, Parasa hilarata causes stings,33 while the Japanese slug caterpillar Latoia (Parasa) lepida has caused several cases of dermatitis.41, 42

Papular urticaria and dermatitis 

Papular urticaria and dermatitis tends to be caused by the setae from hairy or bristly caterpillars or from adult moths (Table III). Most tiger moth caterpillars (family Arctiidae) are wooly or fuzzy, and a number have been reported to cause mild papular pruritic dermatitis. The hickory tussock moth (Lophocampa caryae) is found in the United States from Maine to the Carolinas in late summer, and is easily recognized by its black and white pattern (Fig 15).13 Exposures cause a mildly pruritic eruption that often self resolves within an hour. Direct oral contact has occurred in children, and can cause crying, drooling, refusal to drink, and oral or lip irritation.43 The great tiger moth (Arctia caja) grows to 6 cm in length and is covered with stiff black hairs that may cause a pruritic red scaly papular eruption.33, 44 Several other species in the United States are less commonly reported to cause dermatitis (Table III).

Table III. Species that cause primarily papulourticarial reactions
Common nameSpeciesLocation
Browntail mothEuproctis chrysorrhea1, 2, 3, 4, 13, 61, 62, 63Europe and the US
Gypsy mothLymantria dispar13, 45, 46Europe and the Eastern US
Hickory tussock mothLophocampa caryae13, 43US
White-marked tussock mothOrgyia leucostigma13, 17, 20, 47Eastern US and Canada
Douglas-fir tussock mothO. pseudotsugata48, 49, 50, 51, 52Pacific US
NoneHylesia continua and H frigida5, 136, 137Mexico to Panama
Palometa peluda (little hairy pigeon)Hylesia metabus5, 56, 60, 138South America
NoneHylesia nigricans5Argentina
Asian mulberry tussock mothEuproctis flava70, 71, 72Korea, Japan, and China
NoneEuproctis bipunctapex73Singapore
Japanese tea tussock mothEuproctis pseudoconspersa33, 74Japan
NoneAnthela nicothoe37, 38Australia
White-stemmed gum mothChelepteryx collesi37, 38, 67, 68Australia
Mistletoe browntail mothEuproctis edwardsi64, 65, 66Australia
NoneSpilosoma glatingnyi37, 38Australia
NoneEutane terminalis37, 38Australia
NoneManuela replana37, 38Australia
NonePanacela lewinae37, 38Australia
NoneOrgyia (Teia) anartoides37, 38Australia
NonePorthesia lutea38Australia
NoneAcyphas leucomelas37, 38Australia
NoneLeptocneria reducta37, 38Australia
Australian bag-shelter mothOchrogaster lunifer40, 69Australia
NoneAnaphe venata9, 17, 55Nigeria

US, United States.

In the United States, it is found only in the coastal regions of Maine and Massachusetts.

The gypsy moth (Lymantria dispar) is a well known cause of dermatitis in the northeast United States, where it was introduced from Europe around 1869. The caterpillars are found from May to June, and are recognized by a series of paired warts on the head, with blue and red pairs along the dorsal surface of the caterpillar (Fig 16).13 Contact with L dispar caterpillars causes a pruritic eruption variously described as papular, urticarial, or eczematous, typically most prominent in uncovered areas (Fig 17). The variability in rash morphology may be linked to the multiple pathologic mechanisms involved. The rash is self-limited, lasting approximately 4 to 7 days.45, 46

The white-marked tussock moth caterpillar (Orgyia leucostigma), with a bright red head and prominent yellow or white dorsal tufts, is one of the most easily recognizable caterpillars in the United States (Fig 18). It is found from southern Canada south to Texas.13 Contact with either the caterpillar or cocoon has been reported to cause dermatitis after contact with the skin.17, 20, 47 A closely related caterpillar, the Douglas-fir tussock moth (O pseudotsugata) can be very common on conifer trees in the late spring in the Pacific Northwest United States.48, 49, 50 Contact with these caterpillars causes welts or papular urticaria, although sometimes dermatitis occurs.50, 51, 52 Some series describe the eruption as simply “rash” or “itch.”51

The genus Hylesia comprises about 110 species and is found from Mexico southward throughout South America.5, 53, 54 Female moths (Fig 19) of many species bear hollow abdominal setae5, 12, 55, 56 and contact with the setae on adult moths or setae deposited on egg masses causes pruritic papulourticarial or vesicular eruptions (Fig 20). In Venezuela, where the moths are called palometa peluda (the little hairy pigeon),56 the rash is called Caripito itch, named after the port city of Caripito, where numerous outbreaks have been documented.57, 58 Dermatitis may be widespread, and symptoms can continue for weeks after exposure.56, 57, 58, 59, 60 Even international travelers to endemic areas may return home with dermatitis from exposure to Hylesia.59

In Europe, caterpillars of the browntail moth (Euproctis chrysorrhea) are found from England to the Caucasus Mountains.61, 62, 63 A small population is also found in the United States, centered around southeastern coastal Maine and Cape Cod, although the range of E chrysorrhea in North America formerly extended westward to the Hudson River Valley.13, 61 The caterpillars, which have orange or red abdominal tufts and a characteristic white lateral stripe (Fig 21), cause papulourticarial or eczematous eruptions in exposed areas (Fig 22).1, 2 Although most reactions are mild, some are more severe,1, 2, 3 and at least one death has been attributed to overwhelming allergic reaction to this insect.4

  • View full-size image.
  • Fig 22. 

    Rash from contact with browntail moth caterpillar. (Photograph courtesy of Jan Samanek, State Phytosanitary Administration of the Czech Republic. All rights reserved.)

Two European Lasiocampids, the oak eggar (Lasiocampa quercus) and small eggar (Eriogaster lanestris), have been reported to cause widespread papular urticaria after direct or indirect exposure to the caterpillar setae.44

There are numerous Australian caterpillars that cause dermatitis. The caterpillar of the mistletoe browntail moth (Euproctis edwardsi) is the most common cause of caterpillar dermatitis in Australia.37 Contact with larvae causes pruritic urticarial wheals or papular dermatitis that can be severe.64, 65, 66 Cocoons also bear irritating setae. The larvae are covered with long hairs, but the offending setae, which can embed in human skin, are minute and found only within a white streak along the dorsal surface of the caterpillar.64, 65, 66 A similar species found in the Northern Territory that also causes dermatitis is E stenomorpha.37 Larvae and cocoons of the Australian white-stemmed gum moth (Chelepteryx collesi) bear stiff setae that can penetrate unprotected skin, causing pain, swelling, papular dermatitis, urticaria, or angioedema.37, 38, 67, 68 These caterpillars grow to 10 cm in length and feed on eucalyptus.38 Anthela nicothoe larvae have caused papular dermatitis in pine plantation workers.37 The genus Anthela contains 50 other members in Australia, several of which are known to be urticating.38 The caterpillar of the bag-shelter moth (Ochrogaster lunifer) is found throughout Australia and is often found in long processionary lines feeding on Acacia trees. Contact with the hairy caterpillars may cause severe papular or urticarial dermatitis or ophthalmia nodosa.40, 69 Several other Australian caterpillars are capable of causing papular dermatitis (Table III).

In Asia, there are several species related to the browntail and mistletoe browntail moths that cause papular urticaria or dermatitis. These include the caterpillar and moth of the Asian mulberry tussock moth (E flava) found in China,70, 71, 72 adult moths of E bipunctapex in Singapore,73 the caterpillar of the Japanese tea tussock moth (E pseudoconspersa),33, 74 E flavociliata, and E funeralis.33

Reports of African Lepidoptera causing human disease are woefully inadequate. In Nigeria, adult moths of Anaphe venata may cause dermatitis similar to that of Hylesia.9, 17, 55

Urticarial wheals 

Three species of processionary caterpillars (all belong to the genus Thaumetopoea) cause urticaria or angioedema after contact with caterpillar setae. Two species are commonly known as the pine processionary caterpillar (T wilkinsoni and T pityocampa); both cause human exposures primarily from December to April when the caterpillars can be found feeding on pines.75, 76 T wilkinsoni is found on Cyprus, Israel, Turkey, and the near east,77 whereas T pityocampa (Fig 23) is found in Britain and in Southern Europe.75, 77, 78 The oak processionary caterpillar (T processionea) occurs in southern and central Europe, but in contrast to its pine-feeding cousins it is found during the summer months.79

Contact with caterpillars, cocoons, airborne setae, or soil contaminated with setae from any of these species causes urticaria or angioedema.75, 80, 81, 82, 83, 84, 85 This is consistent with the type I hypersensitivity reactions found in laboratory and clinical experimentation with processionary caterpillars.75, 86, 87, 88, 89, 90, 91 Systemic symptoms, such as vomiting, abdominal pain, hypertension, or anaphylaxis, have only rarely been reported.76, 79, 92, 93 To date, no deaths have been reported in the English medical literature.

Hemorrhagic diathesis (Lonomism) 

Caterpillars of L obliqua and L achelous cause localized stings that may progress to a severe hemorrhagic diathesis termed Lonomism. These gregarious and brightly colored caterpillars bear branched spines (Fig 24) and are found primarily in Brazil and Venezuela (Fig 25).94 Since it was first reported in 1967, approximately 1000 cases have been reported.95 After envenomation, a mild to severe burning pain occurs, often accompanied by headache, nausea, or vomiting. During the next one to several days, cutaneous, mucosal, and visceral hemorrhage ensues (Fig 26). Frank or microscopic hematuria and renal failure may occur. Death may follow from alveolar or intracranial hemorrhage.96, 97, 98, 99 Lemaire5 described 11 species of Lonomia; hemorrhagic diathesis was not seen after envenomation by L electra, but to date, stings to other species have not been reported.5 I advise avoiding contact with all species in this genus.

  • View full-size image.
  • Fig 26. 

    Cutaneous hemorrhage secondary to Lonomia obliqua sting. (Courtesy of Ronaldo Z. Mendonça and Roberto Henrique Pinto Moraes Pesq.Cientìfico-Parasitologia/Entomologia, Instituto Butantan.)

Biting moths 

Six known species of moths from the genus Calyptra have the distinct ability to pierce mammalian skin—including that of humans—with a rasp-like proboscis in order to feed on blood (Fig 27).100 Although the genus Calyptra is widely distributed, including distribution in the United States, only species from southern and Southeast Asia and eastern Russia have been documented to bite humans.100 Only male moths are known to bite.17, 100, 101 Bites from these moths are variously described as painless and transient to intensely painful with swelling that may remain until the next day. Because of the ability to pierce skin, some authors suggest a theoretical risk of transmissible disease.17, 101

Prominent arthritis/arthralgias 

Dendrolimiasis refers to the syndrome of dermatitis and arthritis/chondritis caused by contact with the Masson pine caterpillar (genus Dendrolimus) found in China.102 Both caterpillars and cocoons may cause a self-limited papular or urticarial eruption associated in up to two-thirds of patients with peripheral monoarticular arthropathy that can result in joint destruction.102, 103 Chondritis affecting the costal, thyroid, and auricular cartilages has been described. Soft tissue swelling and pain may also be present. Ophthalmitis has also been reported.102, 103

Pararamose is similar, with a nonspecific pruritic skin eruption associated with a potentially deforming arthritis. It is caused by contact with caterpillars, cocoons, or imagines of the Brazilian moth Premolis semirufa.104, 105

Ophthalmia nodosa 

Caterpillar and tarantula hairs can cause a toxic or allergic eye irritation called ophthalmia nodosa. Setae may be windblown, transferred to the eye via a finger or other fomite, or may result from direct ocular contact with the caterpillar. Unilateral upper lid involvement is typical and begins with chemosis immediately after exposure.106, 107 Patients often have the sense of a foreign body. Chemosis may progress to granuloma formation, iritis, vitritis, retinitis, or endophthalmitis.108, 109 Embedded hairs may slowly migrate to deeper areas of the eye through an unknown mechanism, eventually reaching the optic nerve in some cases.108, 110, 111 Many species (Table IV) have been reported to cause ophthalmia nodosa. In most reports, the offending species is not reported or cannot be identified. Any caterpillar bearing setae may have the potential to cause eye irritation.

Table IV. Caterpillars known to cause ophthalmia nodosa
Thaumetopoea pityocampa110
T wilkinsoni139
Euproctis chrysorrhea110
Anthela spp.106
Hemileuca oliviae140
Dendrolimus punctatus141
Ochrogaster lunifer69
Arctia caja120
Spilosoma virginica142

Oral exposure 

Reports of direct oral exposure to caterpillars are rare. Most cases occur in children, who demonstrate crying, drooling, and lip irritation immediately after exposure. Symptoms include dysphagia, erythema, pain, edema, and pruritus. The most common sites of exposure are the tongue and lips, although the buccal mucosa, palate, hypopharynx, and esophagus may be affected. Setae can be removed with tape stripping in most children with a resolution of the symptoms in 12 to 24 hours40, 43, 112; however, some require admission for observation, direct laryngoscopy, bronchoscopy, and esophagoscopy in the operating room to remove setae embedded in the mucosae.43, 112

Back to Article Outline

Diagnosis and differential diagnosis 

Key points

History of exposure is key to diagnosis

Symptoms and physical examination findings of caterpillar or moth exposure are often nonspecific and the differential may be broad

Geographic location and season may be helpful

An accurate diagnosis of symptoms caused by caterpillars or moths is nearly impossible without a reliable history of exposure. Most symptoms arising from contact with moths and caterpillars are nonspecific, and differential diagnosis is broad. Papular urticaria and eczematous dermatitis are caused by a host of caterpillars and moths (Table III). The differential of papular urticaria include allergies to foods, fragrances and flavorings, medications, metals, plant substances, animal dander or products, preservatives and germicidals, and a host of other chemicals.113, 114 Other causes of papular urticaria include dermatitis herpetiformis, folliculitis, autoeczematization, and other arthropod assaults, including scabies. The differential for eczematous dermatitis caused by caterpillars includes allergic contact dermatitis, irritant dermatitis, autoeczematization, dermatomyositis, eczema, lichen planus, lichen simplex chronicus, seborrheic dermatitis, tinea corporis, and transient acantholytic dermatosis (Grover disease).

Processionary caterpillars (genus Thaumetopoea) typically cause urticaria, angioedema, or anaphylaxis. Urticaria is most commonly associated with recent infection, medication, foods, chemicals, or physical stimulants. In addition, many other insect bites and stings also cause urticarial papules or wheals.

Once exposure has been documented, a focused history on geographic place of exposure can be helpful. Travel to South America, coupled with examination findings of hemorrhage or extensive bruising should trigger laboratory investigation for fibrinolysis caused by Lonomia envenomation. Urticarial wheals after travel to the Mediterranean or Middle East are suggestive of processionary caterpillar (Thaumetopoea) exposure. Acute stings from caterpillars are generally caused by slug caterpillars (Limacodidae), puss caterpillars (Megalopyge), or caterpillars of Hemileucinae (including the io and buck moth caterpillars). Prominent joint symptoms associated with rash after exposure to caterpillars in China is suggestive of Dendrolimus exposure.

There are also other clues. Symptoms related to caterpillar or moth exposure tend to occur on exposed areas. With the exception of the pine processionary caterpillar, caterpillar and moth exposures occur during the summer months, when insects are most prevalent and when people engage in more outdoor activity. However, exposure to tropical insects, especially during international travel, may occur year round. Acute, unilateral ocular inflammation is suggestive of ophthalmia nodosa, and a history of caterpillar exposure should be elicited.

Laboratory work-up in cases of Lepidoptera exposure is useful only in Lonomism. Lonomism is characterized by prolonged prothrombin time, activated partial thromboplastin time, and thrombin time, with characteristic reduction of fibrinogen and normal platelet level. Fibrinogen level may be a marker of disease activity in Lonomism.11

Back to Article Outline

Pathology 

The histology of caterpillar exposure is nonspecific, typically showing epidermal edema, superficial perivascular lymphocytic infiltrate, and eosinophils.16, 115, 116 Epidermal necrosis and vasculitis are rarely seen.57, 117, 118 Embedded spines from Hylesia moths and caterpillars of the browntail moth (Euproctis chrysorrhea) and the puss caterpillar (Megalopyge opercularis) have been described.58, 117, 119 Granulomas with or without embedded caterpillar hairs have been demonstrated in cases of ophthalmia nodosa.108, 110, 120 In addition, granulomas with embedded setae have been seen in both dendrolimiasis and pararamose.103, 104, 105

Back to Article Outline

Treatment 

Key points

Treatments are largely empiric and should be based on symptoms

The removal of spines or hairs should be attempted

Topical steroids and oral antihistamines have been used with mixed success

Puss caterpillar stings may require opioid analgesia

Antivenin should be used for stings caused by L obliqua

See Table V. With the notable exception of L obliqua envenomation, the treatment of adverse events from exposures to Lepidoptera remains symptomatic and supportive. The first line of treatment is the avoidance of offensive species. Heavily infested areas should be avoided by sensitive persons, and caterpillars that bear hairs or spines should not be handled without gloves. For outbreaks or infestations, the manual removal of egg or caterpillar nests or the use of pesticides may be warranted.53, 56, 64, 65, 66, 71, 79, 121, 122, 123 Outdoor lighting should be turned off in areas where Hylesia moths may congregate.53 For those working with Lepidoptera, rearing of caterpillars should be done in a separate room with adequate ventilation and good sanitation. Protective clothing, such as gloves and face masks, may be needed for the routine handling of insects.124

Table V. Treatments for Lepidopteran exposures
Treatment categoryTreatmentLevel of evidence
General recommendationsAvoidance of heavily infested areasIIIc
Manual removal and destruction of caterpillars, cocoons, or egg nestsIIIc
Pesticide applicationIIb
Turning off artificial lightsIIIc
Removal of setae via forceps or cellophane tape strippingIIc
Immediate washing with soap and waterIIIc
Removal of constricting clothing or jewelryIIIc
Laundering of contaminated clothingIIIc
Medical therapyIce, topical pramoxine, or other topical anestheticsIIIc
Topical aspirinIIb
Topical, intralesional, or oral steroidsIIIc
Oral antihistaminesIIIc
Acetaminophen, oral narcotics, or diazepamIIIc
Intravenous calcium gluconateIIIc
Nebulized or subcutaneous epinephrineIIIc
LonomismAntiveninIIb
AntifibrinolyticsIIIc
Ophthalmia nodosaRemoval of setaeIIIc
Topical or oral steroidsIIIc
SurgeryIIIc

Evidence is graded using a 3-point scale based on the quality of methodology as follows: I, good quality patient-oriented evidence; II, limited quality patient-oriented evidence; and III, other evidence including consensus guidelines, extrapolations from bench research, opinion, or case studies. Clinical recommendations are ranked as follows: A, recommendation based on consistent and good quality patient-oriented evidence; B, recommendation based on inconsistent or limited quality patient-oriented evidence; and C, recommendation based on consensus, opinion, or case studies.

For puss caterpillar (Megalopyge opercularis) stings.

For Lonomia obliqua stings.

For Lonomia achelous stings.

Once contact with moths or caterpillars occurs, care should be taken not to rub or scratch the area, nor any attempt to remove or “squash” the insect with a bare hand, because this may further spread irritating setae or spines. Instead, careful removal of the larva with forceps or similar instrument, combined with tape stripping of the area and immediate washing with soap and water, can be effective in minimizing exposure.14, 20, 64, 65, 66, 79 Contaminated clothing should be removed and laundered thoroughly.50, 52

Stinging reactions are often mild and may respond to ice application or use of topical anesthetics, such as pramoxine 1%.26, 29 In more severe stings, particularly after stings from puss caterpillars (Megalopyge opercularis), acetaminophen or narcotics may be needed.28, 29, 39 Diazepam has been used for muscle spasm caused by puss caterpillar envenomation,28 and there are several case reports detailing the successful use of 10% intravenous calcium gluconate for puss caterpillar stings.29, 30, 125

Eczematous reactions are typically treated with mid- to high-potency topical steroids.20, 85, 116, 126 However, response to topical steroids is often ineffective. Topical pramoxine, camphor, or menthol preparations may be useful in these cases. Urticarial reactions may be best treated with antihistamines, and several reports document their usefulness.26, 73, 85, 92 However, a number of reports document the failure of antihistamines to relieve itch.6, 52, 58, 127 Strong recommendations regarding their use cannot be made; however, topical antihistamines may cause allergic contact dermatitis and should be avoided. Because histamine appears to play a role in the eruption caused by many species, topical aspirin may be effective.128 Oral or intramuscular steroids have been useful in some cases20, 24, 126, 127 and ineffective in others.129 Anaphylaxis is rare, but should be treated with subcutaneous epinephrine in a monitored setting. Dendrolimiasis has been successfully treated with antihistamines and oral analgesia but occasionally requires surgical intervention for chondritis or pyarthrosis.102

Ophthalmia nodosa and oral exposure should be managed by a qualified specialist. Most authors suggest immediate irrigation and the removal of setae, under sedation if needed.108, 130 Topical steroids can be used for uveitis or iritis, although granuloma formation may necessitate surgical removal.108, 130 Asymptomatic hairs deep within the eye that cannot easily be extracted may be observed.108, 130 Systemic steroids and antihistamines have been used in several cases of oral exposure.112

Lonomism should be managed by an experienced hematologist. An effective antivenin against Lopap has been produced to counteract the hemorrhagic diathesis from L obliqua envenomation.131, 132 It has been successful in preventing severe hemorrhage in two large series of patients,133, 134 and is considered the cornerstone of current therapy.97 Stings caused by L achelous should be treated with cryoprecipitate, purified fibrinogen, or antifibrinolytic drugs, such as aprotinin and ε-aminocaproic acid.97 It should be noted that antifibrinolytics do not work for stings caused by L obliqua and may exacerbate the clinical symptoms.132, 135 Whole blood and fresh-frozen plasma may worsen hemorrhagic symptoms in stings from both species and should be avoided.97, 135

Back to Article Outline

Conclusions 

Moths and their caterpillars may cause dermatologic or systemic symptoms in humans. Many reactions go unrecognized and may be difficult to diagnose based on their nonspecific symptoms. Dermatitis, urticaria, and localized stings are the most common reactions; however, angioedema, ocular and oral symptoms, anaphylaxis, joint involvement, and hemorrhage may develop. Most therapies are empiric and symptom-driven. An effective antivenin exists for L obliqua envenomation.

Back to Article Outline

References 

  1. Hall-Smith PJ, Graham P. Beware the furry caterpillar. Clin Exp Dermatol. 1980;5:261–262
  2. Blair CP. The browntail moth, its caterpillar and their rash. Clin Exp Dermatol. 1979;4:215–222
  3. Alexander S. The browntail moth, its caterpillar and their rash. Clin Exp Dermatol. 1980;5:261
  4. Kephart CF. The poison glands of the larva of the brown-tail moth (Euproctis chrysorrhoea Linn.). J Parasitol. 1914;1:95–103
  5. Lemaire C. The Saturniidae of America: Hemileucinae. Germany: Antiquariat Geock & Evers. 2002;
  6. Hughes G, Rosen T. Automeris io (caterpillar) dermatitis. Cutis. 1980;26:71–73
  7. Hossler EW, Elston DM, Wagner DL. What's eating you? Io moth (Automeris io. Cutis. 2008;82:21–24
  8. Walker RB, Thomas T, Cupit D, Giaquinto-Shreves J. An epidemic of caterpillar sting dermatitis in a rural West Virginia community. W V Med J. 1993;89:58–60
  9. Bowles DE, Swaby JA. Field guide to venomous and medically important invertebrates affecting military operations: identification, biology, symptoms, treatment. Available at: http://www.afpmb.org/pubs/Field_Guide/field_guide.htm. Accessed October 6, 2008.
  10. Couppié P, Marty C, Sainte-Marie D, Pradinaud R. Poisonous caterpillars in French Guyana. 5 cases. [in French] Ann Dermatol Venereol. 1998;125:489–491
  11. Shevchenko A, de Sousa MM, Waridel P, Bittencourt ST, de Sousa MV, Shevchenko A. Sequence similarity-based proteomics in insects: characterization of the larvae venom of the Brazilian moth Cerodirphia speciosa. J Proteome Res. 2005;4:862–869
  12. Janzen DH. Natural history of Hylesia lineata. J Kansas Entomol Soc. 1984;57:490–514
  13. Wagner DL. Caterpillars of eastern North America: a guide to identification and natural history. Princeton, NJ: Princeton University Press; 2005;
  14. Everson GW, Chapin JB, Normann SA. Caterpillar envenomations: a prospective study of 112 cases. Vet Hum Toxicol. 1990;32:114–119
  15. Tuskes PM, Tuttle JP, Collins MM. The wild silk moths of North America: a natural history of the Saturniidae of the United States and Canada. Ithaca, NY: Cornell University Press; 1996;
  16. Edwards EK, Edwards EK, Kowalczyk AP. Contact urticaria and allergic contact dermatitis to the saddleback caterpillar with histologic correlation. Int J Dermatol. 1986;25:467
  17. Mullen GR. Moths and butterflies (Lepidoptera). In:  Mullen GR,  Durden LA editor. Medical and veterinary entomology. San Diego, CA: Academic Press; 2002;p. 364
  18. Chun S, Hara A, Niino-DuPonte R, Nagamine WT, Conant P, Hirayama C. Stinging nettle caterpillar. Available at: http://www.ctahr.hawaii.edu/oc/freepubs/pdf/IP-22.pdf. Accessed September 22, 2008.
  19. Conant P, Hara AH, Nagamine WT, Kishimoto CM, Heu RA. Nettle caterpillar. Available at: http://www.hawaiiag.org/hdoa/npa/npa01-03-netcat.pdf. Accessed September 22, 2008.
  20. Goddard J. Physician's guide to arthropods of medical importance. 2nd ed. Philadelphia: CRC Press; 1996;
  21. Eagleman DM. Envenomation by the asp caterpillar (Megalopyge opercularis). Clin Toxicol (Phila). 2008;46:201–205
  22. Stipetic ME, Rosen PB, Borys DJ. A retrospective analysis of 96 “asp” (Megalopyge opercularis) envenomations in Central Texas during 1996. J Toxicol Clin Toxicol. 1999;37:457–462
  23. Bishopp FC. The puss caterpillar and the effects of its sting on man. United States Department of Agriculture Department Circulation. 1923;288:1–4
  24. el-Mallakh RS, Baumgartner DL, Fares N. “Sting” of puss caterpillar, Megalopyge opercularis (Lepidoptera: Megalopygidae): first report of cases from Florida and review of literature. J Fla Med Assoc. 1986;73:521–525
  25. Gardner TL, Elston DM. Painful papulovesicles produced by the puss caterpillar. Cutis. 1997;60:125–126
  26. Pinson RT, Morgan JA. Envenomation by the puss caterpillar (Megalopyge opercularis). Ann Emerg Med. 1991;20:562–564
  27. Severs GA, Elston DM. What's eating you? Megalopyge opercularis. Cutis. 2003;71:445–448
  28. Holland DL, Adams DP. “Puss caterpillar” envenomation: a report from North Carolina. Wilderness Environ Med. 1998;9:213–216
  29. McGovern JP, Barkin GD, McElhenney TR, Wende R. Megalopyge opercularis: observations of its life history, natural history of its sting in man, and report of an epidemic. JAMA. 1961;175:1155–1158
  30. Neustater BR, Stollman NH, Manten HD. Sting of the puss caterpillar: an unusual cause of acute abdominal pain. South Med J. 1996;89:826–827
  31. Cates J. Puss caterpillar encounters. Available at: http://www.bugsinthenews.com/puss_caterpillar_encounters.htm. Accessed June 26, 2009.
  32. Ardao MI, Sosa Perdomo C, Pellaton MG. Venom of the Megalopyge urens (Berg) caterpillar. Nature. 1966;209:1139–1140
  33. Henwood BP, MacDonald DM. Caterpillar dermatitis. Clin Exp Dermatol. 1983;8:77–93
  34. Scott HG. Stinging caterpillars. Pest Control. 1964;32:24–25
  35. Derraik J. Erucism in New Zealand: exposure to gum leaf skeletoniser (Uraba lugens) caterpillars in the differential diagnosis of contact dermatitis in the Auckland region. N Z Med J. 2006;119:U2142
  36. Derraik JG. Three students exposed to Uraba lugens (gum leaf skeletoniser) caterpillars in a West Auckland school. N Z Med J. 2007;120:U2656
  37. Common IFB. Moths of Australia. Melbourne: Melbourne University Publishing; 1990;
  38. Southcott R. Moths and butterflies. In:  Covacevich J,  Davie P,  Pearn J editor. Toxic plants and animals: a guide for Australia. 1st ed. Brisbane, Australia: Queensland Museum; 1987;p. 243
  39. Isbister GK, Whelan PI. Envenomation by the billygoat plum stinging caterpillar (Thosea penthima). Med J Aust. 2000;173:654–655
  40. Balit CR, Geary MJ, Russell RC, Isbister GK. Prospective study of definite caterpillar exposures. Toxicon. 2003;42:657–662
  41. Kazunari U. Dermatitis to caterpillar of Latoia lepida. [in Japanese] Rinsho Derma (Tokyo). 2003;45:1549–1550
  42. Takeshi O, Yutaka Y, Tomomichi O. A case of dermatitis from a caterpillar (Latoia lepida). [in Japanese] Jpn J Clin Dermatol. 2004;58:257
  43. Kuspis DA, Rawlins JE, Krenzelok EP. Human exposures to stinging caterpillar: Lophocampa caryae exposures. Am J Emerg Med. 2001;19:396–398
  44. Hellier FF, Warin RP. Caterpillar dermatitis. Br Med J. 1967;2:346–348
  45. Centers for Disease Control and Prevention. Rash illness associated with gypsy moth caterpillars—Pennsylvania. MMWR Morb Mortal Wkly Rep. 1982;31:169–170
  46. Anderson JF, Furniss WE. Epidemic of urticaria associated with first-instar larvae of the gypsy moth (Lepidoptera: Lymantriidae). J Med Entomol. 1983;20:146–150
  47. Goldman L, Sawyer F, Levine A, Goldman J, Goldman S, Spinanger J. Investigative studies of skin irritations from caterpillars. J Invest Dermatol. 1960;34:67–79
  48. Miller JC, Hammond P. Lepidoptera of the Pacific Northwest: caterpillars and adults. US Department of Agriculture, US Forest Service; 2003;
  49. Miller JC, Hammond PC. Macromoths of northwest forests and woodlands. Morgantown, WV: US Department of Agriculture, US Forest Service, Forest Health Technology Enterprise Team; 2000;
  50. Press E, Googins JA, Poareo H, Jones K. Health hazards to timber and forestry workers from the Douglas fir tussock moth. Arch Environ Health. 1977;32:206–210
  51. Redd JT, Voorhees RE, Torok TJ. Outbreak of lepidopterism at a Boy Scout camp. J Am Acad Dermatol. 2007;56:952–955
  52. Hoover AH, Nelson E. Skin symptoms attributed to tussock moth infestation. Cutis. 1974;13:597
  53. Iserhard CA, Kaminski LA, Marchiori MO, Teixeira EC, Romanowski HP. Occurrence of lepidopterism caused by the moth Hylesia nigricans (Berg) (Lepidoptera: Saturniidae) in Rio Grande do Sul state. Brazil. Neotrop Entomol. 2007;36:612–615
  54. Specht A, Formentini AC, Corseuil E. Biological aspects of Hylesia metapyrrha (Lepidoptera; Saturniidae; Hemileucinae), in laboratory. Braz J Biol. 2007;67:173–177
  55. Rodriguez J, Hernandez JV, Fornes L, Lundberg U, Arocha-Pinango CL, Osborn F. External morphology of abdominal setae from male and female Hylesia metabus adults (Lepidoptera: Saturniidae) and their function. Fla Entomol. 2004;87:30–36
  56. Benaim-Pinto C, Pernia-Rosales B, Rojas-Peralta R. Dermatitis caused by moths of Hylesia genus (Lepidoptera, Saturniidae) in northeastern states of Venezuela: I. Bioecology of Hylesia metabus (Cramer). Clinical features of lepidopterism determined by this species. Am J Contact Derm. 1991;2:213
  57. Zaias N, Ioannides G, Taplin D. Dermatitis from contact with moths (genus Hylesia). JAMA. 1969;207:525–527
  58. Dinehart SM, Archer ME, Wolf JE, McGavran MH, Reitz C, Smith EB. Caripito itch: dermatitis from contact with Hylesia moths. J Am Acad Dermatol. 1985;13:743–747
  59. Jamieson F, Keystone JS, From L, Rosen C. Moth-associated dermatitis in Canadian travellers returning from Mexico. CMAJ. 1991;145:1119–1121
  60. Rodriguez-Morales AJ, Arria M, Rojas-Mirabal J, Borges E, Benitez JA, Herrera M, et al. Lepidopterism due to exposure to the moth Hylesia metabus in northeastern Venezuela. Am J Trop Med Hyg. 2005;73:991–993
  61. Ferguson DC. Noctuoidea, Lymantriidae, vol. 22-2. London: E.W. Classey; 1978;
  62. Henshaw S. Euproctis chrysorrhoea in Massachusetts. Science. 1897;5:845–846
  63. de Jong MC, Bleumink E, Nater JP. Investigative studies of the dermatitis caused by the larva of the brown-tail moth (Euproctis chrysorrhoea Linn.) I. Clinical and experimental findings. Arch Dermatol Res. 1975;253:287–300
  64. Dunlop K, Freeman S. Caterpillar dermatitis. Australas J Dermatol. 1997;38:193–195
  65. Scholz A, Russell R, Geary M. Investigation of caterpillar dermatitis in school children. NSW Public Health Bull. 1993;4:65–66
  66. Balit CR, Ptolemy HC, Geary MJ, Russell RC, Isbister GK. Outbreak of caterpillar dermatitis caused by airborne hairs of the mistletoe browntail moth (Euproctis edwardsi). Med J Aust. 2001;175:641–643
  67. Balit CR, Geary MJ, Russell RC, Isbister GK. Clinical effects of exposure to the white-stemmed gum moth (Chelepteryx collesi). Emerg Med Australas. 2004;16:74–81
  68. Mulvaney JK, Gatenby PA, Brookes JG. Lepidopterism: two cases of systemic reactions to the cocoon of a common moth, Chelepteryx collesi. Med J Aust. 1998;168:610–611
  69. Burwell C. Bag-shelter moths and processionary caterpillars. Available at: http://www.qm.qld.gov.au/inquiry/factsheets/bag-shelter_moths_20080709.pdf. Accessed October 2, 2008.
  70. Tsutsumi C. A histological study of the development of the urticating spicules of the Far Eastern urticating moth, Euproctis flava Bremer (Lepidoptera: Lymantriidae). Jpn J Med Sci Biol. 1958;11:443–453
  71. De-Long S. Mulberry tussock moth dermatitis. A study of an epidemic of unknown origin. J Epidemiol Community Health. 1981;35:1–4
  72. Mills RG. Observations on a series of case of dermatitis caused by a Liparid moth, Euproctis flava. Chin Med J. 1923;37:351–371
  73. Ooi PL, Goh KT, Lee HS, Goh CL. Tussockosis: an outbreak of dermatitis caused by tussock moths in Singapore. Contact Derm. 1991;24:197–200
  74. Natsuaki M. Immediate and delayed-type reactions in caterpillar dermatitis. J Dermatol. 2002;29:471–476
  75. Fuentes Aparicio V, de Barrio Fernández M, Rubio Sotés M, Rodríguez Paredes A, Martínez Molero MI, Zapatero Remón L, et al. Non-occupational allergy caused by the pine processionary caterpillar (Thaumetopoea pityocampa). Allergol Immunopathol. 2004;32:69–75
  76. Finkelstein Y, Raikhlin-Eisenkraft B, Taitelman U. Systemic manifestations of erucism: a case report. Vet Hum Toxicol. 1988;30:573–574
  77. Bruchim Y, Ranen E, Saragusty J, Aroch I. Severe tongue necrosis associated with pine processionary moth (Thaumetopoea wilkinsoni) ingestion in three dogs. Toxicon. 2005;45:443–447
  78. Turkmen H, Ali Oner Y. A human dermatitis caused by Thaumetopoea pityocampa (Denis and Schiffermuller, 1775) (order: Lepidoptera) caterpillars in Istanbul, Turkey. Allergy. 2004;59:232–233
  79. Gottschling S, Meyer S, Dill-Mueller D, Wurm D, Gortner L. Outbreak report of airborne caterpillar dermatitis in a kindergarten. Dermatology. 2007;215:5–9
  80. Ziprkowski L, Hofshi E, Tahori AS. Caterpillar dermatitis. Isr Med J. 1959;18:26–31
  81. Gottschling S, Meyer S. An epidemic airborne disease caused by the oak processionary caterpillar. Pediatr Dermatol. 2006;23:64–66
  82. Garty BZ, Danon YL. Processionary caterpillar dermatitis. Pediatr Dermatol. 1985;2:194–196
  83. Shkalim V, Herscovici Z, Amir J, Levy Y. Systemic allergic reaction to tree processionary caterpillar in children. Pediatr Emerg Care. 2008;24:233–235
  84. Spiegel W, Maier H, Maier M. A non-infectious airborne disease. Lancet. 2004;363:1438
  85. Maier H, Spiegel W, Kinaciyan T, Krehan H, Cabaj A, Schopf A, et al. The oak processionary caterpillar as the cause of an epidemic airborne disease: survey and analysis. Br J Dermatol. 2003;149:990–997
  86. Vega JM, Moneo I, Armentia A, Fernández A, Vega J, De La Fuente R, et al. Allergy to the pine processionary caterpillar (Thaumetopoea pityocampa). Clin Exp Allergy. 1999;29:1418–1423
  87. Vega J, Vega JM, Moneo I, Armentia A, Caballero ML, Miranda A. Occupational immunologic contact urticaria from pine processionary caterpillar (Thaumetopoea pityocampa): experience in 30 cases. Contact Dermatitis. 2004;50:60–64
  88. Vega JM, Moneo I, Armentia A, Vega J. De la Fuente R, Fernandez A. Pine processionary caterpillar as a new cause of immunologic contact urticaria. Contact Dermatitis. 2000;43:129–132
  89. Fuentes Aparicio V, Zapatero Remon L, Martinez Molero MI, Alonso Lebreros E, Beitia Mazuecos JM, Bartolome Zavala B. Allergy to pine processionary caterpillar (Thaumetopoea pityocampa) in children. Allergol Immunopathol. 2006;34:59–63
  90. Lamy M, Pastureaud MH, Novak F, Ducombs G, Vincendeau P, Maleville J, et al. Thaumetopoein: an urticating protein from the hairs and integument of the pine processionary caterpillar (Thaumetopoea pityocampa Schiff., Lepidoptera, Thaumetopoeidae). Toxicon. 1986;24:347–356
  91. Werno J, Lamy M, Vincendeau P. Caterpillar hairs as allergens. Lancet. 1993;342:936–937
  92. Kozer E, Lahat E, Berkovitch M. Hypertension and abdominal pain: uncommon presentation after exposure to a pine caterpillar. Toxicon. 1999;37:1797–1801
  93. Vega JM, Moneo I, Armentia A, López-Rico R, Curiel G, Bartolomé B, et al. Anaphylaxis to a pine caterpillar. Allergy. 1997;52:1244–1245
  94. Veiga AB, Blochtein B, Guimarães JA. Structures involved in production, secretion and injection of the venom produced by the caterpillar Lonomia obliqua (Lepidoptera, Saturniidae). Toxicon. 2001;39:1343–1351
  95. Arocha-Pinango CL, Marval E, Guerrero B. Lonomia genus caterpillar toxins: biochemical aspects. Biochimie. 2000;82:937–942
  96. Chan K, Lee A, Onell R, Etches W, Nahirniak S, Bagshaw SM, et al. Caterpillar-induced bleeding syndrome in a returning traveller. CMAJ. 2008;179:158–161
  97. Chudzinki-Tavassi AM, Carrijo-Carvalho LC. Biochemical and biological properties of Lonomia obliqua bristle extract. J Venom Anim Toxins incl Trop Dis. 2006;12:159–171
  98. Arocha-Piñango CL, de Bosch NB, Torres A, Goldstein C, Nouel A, Argüello A, et al. Six new cases of a caterpillar-induced bleeding syndrome. Thromb Haemost. 1992;67:402–407
  99. Gamborgi GP, Metcalf EB, Barros EJ. Acute renal failure provoked by toxin from caterpillars of the species Lonomia obliqua. Toxicon. 2006;47:68–74
  100. Zaspel VS, Kononenko VS, Goldstein PZ. Another blood feeder? Experimental feeding of a fruit-piercing moth species on human blood in the Primorye territory of far eastern Russia (Lepidoptera: Noctuidae: Calpinae). J Insect Behav. 2007;20:437–451
  101. Banziger H. Skin-piercing blood-sucking moths II: studies on a further 3 adult Calyptra [Calpe] sp. (Lepid., Noctuidae). Acta Trop. 1979;36:23–37
  102. Huang DZ. Dendrolimiasis: an analysis of 58 cases. J Trop Med Hyg. 1991;94:79–87
  103. Lawson JP, Liu YM. Pinemoth caterpillar disease. Skeletal Radiol. 1986;15:422–427
  104. Costa RM, Atra E, Ferraz MB, da Silva NP, de Souza JM, Batista Júnior J, et al. “Pararamose”: an occupational arthritis caused by lepidoptera (Premolis semirufa). An epidemiological study. Rev Paul Med. 1993;111:462–465
  105. Dias LB, de Azevedo MC. Pararama, a disease caused by moth larvae: experimental findings. Pathol Bull. 1973;7:9–14
  106. Bishop JW, Morton MR. Caterpillar-hair keratoconjunctivitis. Am J Ophthalmol. 1967;64:778–779
  107. Sood P, Tuli R, Puri R, Sharma R. Seasonal epidemic of ocular caterpillar hair injuries in the Kangra district of India. Ophthalmic Epidemiol. 2004;11:3–8
  108. Cadera W, Pachtman MA, Fountain JA, Ellis FD, Wilson 2nd FM. Ocular lesions caused by caterpillar hairs (ophthalmia nodosa). Can J Ophthalmol. 1984;19:40–44
  109. Steele C, Lucas DR, Ridgway AE. Endophthalmitis due to caterpillar setae: surgical removal and electron microscopic appearances of the setae. Br J Ophthalmol. 1984;68:284–288
  110. Watson PG, Sevel D. Ophthalmia nodosa. Br J Ophthalmol. 1966;50:209–217
  111. Fraser SG, Dowd TC, Bosanquet RC. Intraocular caterpillar hairs (setae): clinical course and management. Eye. 1994;8:596–598
  112. Lee D, Pitetti RD, Casselbrant ML. Oropharyngeal manifestations of lepidopterism. Arch Otolaryngol Head Neck Surg. 1999;125:50–52
  113. Burdick AE, Mathias CG. The contact urticaria syndrome. Dermatol Clin. 1985;3:71–84
  114. Chudzinski-Tavassi AM, Alvarez Flores MP. Exploring new molecules and activities from Lonomia obliqua caterpillars. Pathophysiol Haemost Thromb. 2005;34:228–233
  115. de Jong MC, Hoedemaeker J, Jongebloed WL, Nater JP. Investigative studies of the dermatitis caused by the larva of the brown-tail moth (Euproctis chrysorrhoea Linn.) II. Histopathology of skin lesions and scanning electron microscopy of their causative setae. Arch Dermatol Res. 1976;255:177–191
  116. Allen VT, Miller OF, Tyler WB. Gypsy moth caterpillar dermatitis—revisited. J Am Acad Dermatol. 1991;24(pt 6):979–981
  117. Foot NC. Pathology of the dermatitis caused by Megalopyge opercularis, a Texan caterpillar. J Exp Med. 1922;35:737–753
  118. Benvenuti LA, Cardoso JL, Moraes RH. Cutaneous leucocytoclastic vasculitis from contact with Hylesia moths (Lepidoptera: Saturniidae). Trans R Soc Trop Med Hyg. 1998;92:428–429
  119. Tyzzer EE. The pathology of the brown-tail moth dermatitis. J Med Res. 1907;16:43–64
  120. Corkey JA. Ophthalmia nodosa due to caterpillar hairs. Br J Ophthalmol. 1955;39:301–306
  121. Liebhold S. Gypsy moth in North America. Available at: http://www.fs.fed.us/ne/morgantown/4557/gmoth/. Accessed April 11, 2008.
  122. Hesler LS, Logan TM, Benenson MW, Moser C. Acute dermatitis from oak processionary caterpillars in a U.S. military community in Germany. Mil Med. 1999;164:767–770
  123. Salomon OD, Simon D, Rimoldi JC, Villaruel M, Perez O, Perez R, et al. Lepidopterism due to the butterfly Hylesia nigricans. Preventive research-intervention in Buenos Aires. [in Spanish] Medicina (B Aires). 2005;65:241–246
  124. Wirtz RA. Occupational allergies to arthropods—documentation and prevention. Bull Entomol Soc Am. 1980;26:356–360
  125. Micks DW. Clinical effects of the sting of the “puss caterpillar” (Megalopyge opercularis S & A) on man. Tex Rep Biol Med. 1952;10:399–405
  126. Knuckles ML, Hodge SJ, White AF. Fall webworm dermatitis. Int J Dermatol. 1987;26:320–321
  127. Beaucher WN, Farnham JE. Gypsy-moth-caterpillar dermatitis. N Engl J Med. 1982;306:1301–1302
  128. Yosipovitch G, Ademola J, Lui P, Amin S, Maibach HI. Topically applied aspirin rapidly decreases histamine-induced itch. Acta Derm Venereol. 1997;77:46–48
  129. Rosen T. Caterpillar dermatitis. Dermatol Clin. 1990;8:245–252
  130. Teske SA, Hirst LW, Gibson BH, O'Connor PA, Watts WH, Carey TM. Caterpillar-induced keratitis. Cornea. 1991;10:317–321
  131. Da Silva WD, Campos CM, Gonçalves LR, Sousa-e-Silva MC, Higashi HG, Yamagushi IK, et al. Development of an antivenom against toxins of Lonomia obliqua caterpillars. Toxicon. 1996;34:1045–1049
  132. Rocha-Campos AC, Gonçalves LR, Higashi HG, Yamagushi IK, Fernandes I, Oliviera JE, et al. Specific heterologous F(ab')2 antibodies revert blood incoagulability resulting from envenoming by Lonomia obliqua caterpillars. Am J Trop Med Hyg. 2001;64:283–289
  133. Zannin M, Lourenco DM, Motta G, Dalla Costa LR, Grando M, Gamborgi GP, et al. Blood coagulation and fibrinolytic factors in 105 patients with hemorrhagic syndrome caused by accidental contact with Lonomia obliqua caterpillar in Santa Catarina, southern Brazil. Thromb Haemost. 2003;89:355–364
  134. Caovilla JJ, Barros EJ. Efficacy of two different doses of antilonomic serum in the resolution of hemorrhagic syndrome resulting from envenoming by Lonomia obliqua caterpillars: a randomized controlled trial. Toxicon. 2004;43:811–818
  135. Gonçalves LR, Sousa-e-Silva MC, Tomy SC, Sano-Martins IS. Efficacy of serum therapy on the treatment of rats experimentally envenomed by bristle extract of the caterpillar Lonomia obliqua: Comparison with epsilon-aminocaproic acid therapy. Toxicon. 2007;50:349–356
  136. Centers for Disease Control and Prevention. Moth-associated dermatitis—Cozumel, Mexico. MMWR Morb Mortal Wkly Rep. 1990;39:219–220
  137. Fernandez G, Morales E, Beutelspacher C, Villanueva A, Ruiz C, Stetler HC. Epidemic dermatitis due to contact with a moth in Cozumel, Mexico. Am J Trop Med Hyg. 1992;46:560–563
  138. Lundberg U, Salazar V, Tovar M, Rodriguez J. Isolation and partial characterization of proteins with vasodegenerative and proinflammatory properties from the egg-nests of Hylesia metabus (Lepidoptera: Saturniidae). J Med Entomol. 2007;44:440–449
  139. Bessler E, Biedner B, Yassur Y. Thaumetopoea wilkinsoni (toxic pine caterpillars) blepharoconjunctivitis. Am J Ophthalmol. 1987;103:117–118
  140. Caffrey DJ. Notes of the poisonous urticating spines of Hemileuca oliviae larvae. J Econ Entomol. 1918;11:363–367
  141. Horng CT, Chou PI, Liang JB. Caterpillar setae in the deep cornea and anterior chamber. Am J Ophthalmol. 2000;129:384–385
  142. Lertchavanakul A, Pearce WG, Nigam S. Ophthalmia nodosa. Can J Ophthalmol. 1975;10:86–89

 Funding sources: None.

 The authors, editors, and peer reviewers have no relevant financial relationships.

PII: S0190-9622(09)01235-3

doi:10.1016/j.jaad.2009.08.061

Journal of the American Academy of Dermatology
Volume 62, Issue 1 , Pages 13-28, January 2010