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10.1136/bcr-2013-009739 http://scihub22266oqcxt.onion/10.1136/bcr-2013-009739 C3822268!3822268!24127370     free     free     free       BMJ+Case+Rep 2013 ; 2013 (ä): ä Nephropedia Template TP {{tp|p=24127370|t=2013. Febrile ulceronecrotic Mucha-Habermann disease |pdf=|usr=}}{{24127370}} gab.com Text Febrile ulceronecrotic Mucha-Habermann disease JO: BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=24127370 #FOAvip 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. Twit Text FOAVip Febrile ulceronecrotic Mucha-Habermann disease ????BMJ Case Rep http://www.kidney.de/pget.php?&tw=1&pmid=24127370 #FOAvip Twit Text # Free Paper on # # # # # LINK http://www.kidney.de/pget.php?&tw=1&pmid=24127370 #FOAvip English Wikipedia <ref>{{Cite pmid|24127370}}</ref> Febrile ulceronecrotic Mucha-Habermann disease #MMPMID24127370 Lejuste FX; Michaux C; Lehners C; Calteux N BMJ Case Rep 2013[]; 2013 (ä): ä PMID24127370show ga 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. äFebrile ulceronecrotic Mucha-Habermann disease (epmc).pdf DeepDyve Pubget Overpricing