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Lichenoid drug eruption following intravenous application of orally formulated diamorphine, a semisynthetic heroin

Kolm, Isabel; Eggmann, N; Kamarashev, J; Kerl, K; French, L E; Hofbauer, G F L (2013). Lichenoid drug eruption following intravenous application of orally formulated diamorphine, a semisynthetic heroin. Case Reports in Dermatology, 5(2):176-180.

Abstract

BACKGROUND: Lichen planus is a common skin disorder of unknown etiology. Most cases are idiopathic, but substances such as gold, antimalarials, penicillamine, thiazide diuretics, β-blockers, arsenic and nonsteroidal anti-inflammatory drugs have been implicated as trigger factors.
CASE PRESENTATION: We report the case of a lichenoid eruption in a male drug addict who administered oral heroin (diamorphine) intravenously. Diamorphine was stopped immediately. Following topical steroids, phototherapy and oral acitretin, the lesions gradually disappeared. A lymphocyte transformation test was negative for pure morphine and codeine.
DISCUSSION: A coincidental association between the intravenous application of orally formulated semisynthetic heroin and the lichenoid eruption cannot be completely ruled out. However, the diagnosis of a lichenoid drug eruption is favoured over idiopathic lichen planus because of the clear chronological correlation between drug use and appearance as well as drug withdrawal and disappearance of the skin lesions, and because of a flare-up following repeated intravenous application of diamorphine.

Additional indexing

Item Type:Journal Article, refereed, further contribution
Communities & Collections:04 Faculty of Medicine > University Hospital Zurich > Dermatology Clinic
Dewey Decimal Classification:610 Medicine & health
Scopus Subject Areas:Health Sciences > Dermatology
Uncontrolled Keywords:Drug eruption, Diamorphine, Synthetic heroin, Lichen planus
Language:English
Date:2013
Deposited On:07 Jan 2014 15:59
Last Modified:29 Jan 2025 04:30
Publisher:Karger
ISSN:1662-6567
OA Status:Gold
Free access at:PubMed ID. An embargo period may apply.
Publisher DOI:https://doi.org/10.1159/000353305
PubMed ID:23874294
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