Febrile ulceronecrotic Mucha-Habermann disease: A case report and a review of the literature

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dc.contributor.authorAytekin S.
dc.contributor.authorBalci G.
dc.contributor.authorDuzgun O.Y.
dc.date.accessioned2024-04-24T18:43:49Z
dc.date.available2024-04-24T18:43:49Z
dc.date.issued2005
dc.departmentDicle Üniversitesien_US
dc.description.abstractWe report a case of febrile ulceronecrotic Mucha-Habermann disease (FUMHD) in a 27-year-old woman. After 20 days of a mild eruption, extensive polymorphous, papular and ulcerohemorrhagic skin lesions gradually developed, associated with intermittent high temperature, and constitutional symptoms. The initial treatment with acyclovir was not successful, the skin lesions still progressed distally and individual lesions evolved from necrotic papules and bullae to erosions and ulcers. Skin biopsies showed the typical histopathological changes of PLEVA. The patient was treated with systemic prednisolone but dosage was limited in order to avoid sepsis. Despite corticosteroid therapy and supportive therapy, the fulminating course led to death. Including this present case, only 31 cases of FUMHD have been reported in English literature. Our case is the second report from Turkey. © 2005 Dermatology Online Journal.en_US
dc.identifier.issn1087-2108
dc.identifier.issue3en_US
dc.identifier.pmid16409927
dc.identifier.scopus2-s2.0-33746810654
dc.identifier.scopusqualityQ3
dc.identifier.urihttps://hdl.handle.net/11468/24402
dc.identifier.volume11en_US
dc.indekslendigikaynakScopus
dc.indekslendigikaynakPubMed
dc.language.isoenen_US
dc.relation.ispartofDermatology Online Journal
dc.relation.publicationcategoryMakale - Uluslararası Hakemli Dergi - Kurum Öğretim Elemanıen_US
dc.rightsinfo:eu-repo/semantics/closedAccessen_US
dc.titleFebrile ulceronecrotic Mucha-Habermann disease: A case report and a review of the literatureen_US
dc.titleFebrile ulceronecrotic Mucha-Habermann disease: A case report and a review of the literature
dc.typeReview Articleen_US

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