You are in: eMedicine Specialties > Dermatology > ENVIRONMENTAL Seabather's EruptionArticle Last Updated: Oct 2, 2006AUTHOR AND EDITOR INFORMATIONAuthor: Clarence William Brown, Jr, MD, Consulting Surgeon, Department of Dermatology, Assistant Professor of Dermatology, Rush-Presbyterian-St. Luke's Medical Center Clarence William Brown, Jr, is a member of the following medical societies: American Academy of Dermatology and American College of Mohs Micrographic Surgery and Cutaneous Oncology Editors: Carrie L Kovarik, MD, Assistant Professor, Department of Dermatology and Dermatopathology, University of Pennsylvania School of Medicine; Richard P Vinson, MD, Assistant Clinical Professor, Department of Dermatology, Texas Tech University School of Medicine; Consulting Staff, Mountain View Dermatology, PA; Jeffrey P Callen, MD, Professor of Medicine, Chief, Division of Dermatology, University of Louisville School of Medicine; Joel M Gelfand, MD, MSCE, Medical Director, Clinical Studies Unit, Assistant Professor, Department of Dermatology, Associate Scholar, Center for Clinical Epidemiology and Biostatistics, University of Pennsylvania; William D James, MD, Paul R Gross Professor of Dermatology, University of Pennsylvania School of Medicine; Vice-Chair, Program Director, Department of Dermatology, University of Pennsylvania Health System Author and Editor Disclosure Synonyms and related keywords: sea lice, Linuche unguiculata, L unguiculata, thimble jellyfish larvae INTRODUCTIONBackgroundSeabather's eruption was first described in 1949 as a pruritic papular eruption occurring in bathers off the eastern coast of Florida. Seabather's eruption is a highly pruritic, papular eruption that occurs underneath the swimsuit after extended exposure to seawater. Seabather's eruption results from a hypersensitivity to the larval form of the thimble jellyfish, Linuche unguiculata. Most cases occur from March to August, but the incidence peaks in May and June. PathophysiologySeabather's eruption is a cutaneous hypersensitivity reaction to the larval form (planulae) of the thimble jellyfish, L unguiculata. The eruption typically occurs underneath the bathing garments, which are believed to trap the jellyfish larvae against the skin. Whether the discharge of venom by the trapped larvae plays an important role in the pathogenesis of the eruption remains uncertain. Factors that promote the discharge of venom by the larvae include wearing of bathing suits for prolonged periods following swimming, exposure to fresh water through showering, and mechanical stimulation. FrequencyUnited StatesThe incidence of seabather's eruption is seasonal; the highest incidence occurs from May through August. This coincides with the warm gulf streams running along the Atlantic coastline of Florida and the corresponding spawn of thimble jellyfish larvae, which results in the high seasonal concentration of Linuche planulae. In 1997, Kumar et al reported the occurrence of seabather's eruption in Palm Beach saltwater swimmers in May to be 16%. InternationalSeabather's eruption has been reported in Mexico and the Caribbean. The true prevalence of seabather's eruption along international coastlines remains unknown. Mortality/MorbidityNo deaths have been attributed to exposure to thimble jellyfish larvae. SexSeabather's eruption has been noted with equal frequency in both sexes. AgeNo correlation between age and risk for developing seabather's eruption has been noted. The severity of symptoms, particularly the frequency of fever, is greater in children than in adults. CLINICALHistoryThe eruption begins a few hours after bathing in the ocean.
PhysicalOn physical examination, patients with seabather's eruption typically display inflammatory papules in a distribution pattern that mimics the bathing suit. Lesions have been noted to occur in the axillae; in men with significant chest hair, they occur on the chest.
CausesSeabather's eruption is caused by exposure to the larval form (planulae) of the thimble jellyfish, L unguiculata.
DIFFERENTIALSChickenpox Contact Dermatitis, Allergic Eosinophilic Pustular Folliculitis Folliculitis Id Reaction (Autoeczematization) Insect Bites Jellyfish Stings Lymphomatoid Papulosis Papular Urticaria Parapsoriasis Psoriasis, Guttate Urticaria, Acute
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| Drug Name | Clobetasol (Temovate) |
|---|---|
| Description | Class I superpotent topical steroid; suppresses mitosis and increases synthesis of proteins that decrease inflammation and cause vasoconstriction. Potent anti-inflammatory properties. Do not use in groin, axilla, or face. |
| Adult Dose | Apply to affected areas bid for up to 2 wk; not to exceed 50 g/wk |
| Pediatric Dose | Apply sparingly to affected areas bid for 1 wk; limit administration to least amount compatible with effective therapy |
| Contraindications | Documented hypersensitivity; viral or fungal skin infections |
| Interactions | None reported |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Prolonged exposure to topical corticosteroids can lead to thinning and atrophy of skin as well as suppression of hypothalamic-pituitary-adrenal axis; limit application in adults to no longer than 2 wk; <50 g weekly to avoid above complications |
These agents prevent histamine response in sensory nerve endings and blood vessels. They are more effective in preventing histamine response than in reversing it. They also reduce pruritus.
| Drug Name | Loratadine (Claritin) |
|---|---|
| Description | Second-generation antihistamine with very low risk of sedation. Selectively inhibits peripheral histamine H1 receptors. |
| Adult Dose | 10 mg PO qd |
| Pediatric Dose | <2 years: Not established 2-6 years: 5 mg/d PO >6 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Ketoconazole, erythromycin, procarbazine, and alcohol may increase levels |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Initiate therapy at lower dose in liver impairment |
| Drug Name | Cetirizine (Zyrtec) |
|---|---|
| Description | Second-generation antihistamine with low risk of sedation. Forms complex with histamine for H1 receptor sites in blood vessels, GI tract, and respiratory tract. |
| Adult Dose | 5-10 mg PO qd |
| Pediatric Dose | <2 years: Not established 2-5 years: 2.5 mg PO qd >5 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Increases CNS toxicity of depressants |
| Pregnancy | B - Usually safe but benefits must outweigh the risks. |
| Precautions | Caution in hepatic or renal dysfunction; doses >10 mg/d may cause drowsiness |
| Drug Name | Desloratadine (Clarinex) |
|---|---|
| Description | Long-acting tricyclic histamine antagonist selective for H1 receptor. Relieves nasal congestion and systemic effects of seasonal allergy. Is a major metabolite of loratadine, which, after ingestion, is metabolized extensively to active metabolite 3-hydroxydesloratadine. |
| Adult Dose | 5 mg PO qd |
| Pediatric Dose | <12 years: Not established >12 years: Administer as in adults |
| Contraindications | Documented hypersensitivity |
| Interactions | Limited data exist; erythromycin and ketoconazole increase desloratadine and 3-hydroxydesloratadine plasma concentrations, but no increase in clinically relevant adverse effects, including QTc, was observed |
| Pregnancy | C - Safety for use during pregnancy has not been established. |
| Precautions | Decrease dose in hepatic impairment; rarely causes pharyngitis or dry mouth |
Article Last Updated: Oct 2, 2006