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Article ; Online: Febrile ulceronecrotic Mucha-Habermann disease.

Lejuste, F-X / Michaux, C / Lehners, C / Calteux, N

BMJ case reports

2013  Volume 2013

Abstract: The Mucha-Habermann disease is an inflammatory disease of the skin and is a variant of pityriasis lichenoides et varioliformis acuta. We describe the case of a 64-years-old woman who was admitted for erysipelas of the face. Despite treatment, evolution ... ...

Abstract The Mucha-Habermann disease is an inflammatory disease of the skin and is a variant of pityriasis lichenoides et varioliformis acuta. We describe the case of a 64-years-old woman who was admitted for erysipelas of the face. Despite treatment, evolution was marked by the appearance of a necrotising ulcerative area in the centre of the erysipelas associated with local oedema and headache. A skin biopsy revealed a pityriasis lichenoides et varioliformis acuta. Corticosteroids led to a rapid stabilisation of lesions, and after 6 months the patient shows only a small area of frontal hypopigmentation. The aetiology remains uncertain. There is no established standard treatment. We would like to draw attention of the medical and surgical specialists to this rare disease. The diagnosis should be considered in a necrotic lesion associated with rapid expansion of systemic and peripheral cutaneous signs. Diagnosis must be considered to avoid unnecessary debridement and extensive scars.
MeSH term(s) Diagnosis, Differential ; Erysipelas/diagnosis ; Erysipelas/pathology ; Female ; Forehead ; Humans ; Middle Aged ; Necrosis ; Pityriasis Lichenoides/diagnosis ; Pityriasis Lichenoides/pathology ; Skin Ulcer/diagnosis ; Skin Ulcer/pathology
Language English
Publishing date 2013-10-14
Publishing country England
Document type Case Reports ; Journal Article
ISSN 1757-790X
ISSN (online) 1757-790X
DOI 10.1136/bcr-2013-009739
Database MEDical Literature Analysis and Retrieval System OnLINE

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