Primary cutaneous mucormycosis presenting as a giant plaque: uncommon presentation of a rare mycosis.

Abstract:

:Mucormycosis is an uncommon systemic mycosis affecting the immunocompromised individuals. It is usually caused by organisms of the genera Rhizopus and Mucor, although rarely other organisms have also been implicated. Mycoses due to these angioinvasive fungi have an acute onset, rapidly progressive course with high mortality rate. A rare and less well known is the chronic subtype of primary cutaneous mucormycosis (PCM). Herein, we report a case of PCM clinically presenting as a chronic, giant destructive plaque in a young immunocompetent male and coin the term chronic granulomatous mucormycosis. A clinicopathological classification for cutaneous mucormycosis is also proposed.

journal_name

Mycopathologia

journal_title

Mycopathologia

authors

Vinay K,Chandrasegaran A,Kanwar AJ,Saikia UN,Kaur H,Shivaprakash MR,Dogra S

doi

10.1007/s11046-014-9752-6

subject

Has Abstract

pub_date

2014-08-01 00:00:00

pages

97-101

issue

1-2

eissn

0301-486X

issn

1573-0832

journal_volume

178

pub_type

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