Nephrogenic fibrosing dermopathy – a rare case.

Mahesh Kumar Usha, Balasaheb Ramling Yelikar  Aparna Palit  Saurabh Srivastava

dc.contributor.author	Mahesh Kumar Usha, Balasaheb Ramling Yelikar Aparna Palit Saurabh Srivastava
dc.date.accessioned	2020-01-22T07:11:48Z
dc.date.available	2020-01-22T07:11:48Z
dc.date.issued	2012-04
dc.identifier.uri	http://hdl.handle.net/123456789/1784
dc.description.abstract	The aim of the article is to present a rare case of nephrogenic fibrosing dermopathy (NFD) in a 54 year old male, which has been recently described fibrosing disorder that emerges in different settings of renal insufficiency. These are characterized by skin- coloured to erythematous papules that coalesce into plaques markedly thickened in texture. To date, the registry for NFD lists approximately 175 cases worldwide. In our case, clinical features, histopathology, special stains and immunohistochemistry were diagnostic of NFD.	en_US
dc.language.iso	en	en_US
dc.publisher	BLDE(Deemed to be University)	en_US
dc.subject	Nephrogenic Fibrosing Dermopathy, Chronic Renal Failure, Histopathology	en_US
dc.title	Nephrogenic fibrosing dermopathy – a rare case.	en_US
dc.type	Article	en_US