Bullous pemphigoid.

dc.contributor.author	Khandpur, Sujay
dc.contributor.author	Verma, Parul
dc.date.accessioned	2012-08-31T05:38:29Z
dc.date.available	2012-08-31T05:38:29Z
dc.date.issued	2011-07
dc.description.abstract	Bullous pemphigoid (BP) is a relatively common autoimmune vesicobullous disease encountered in India. It is a subepidermal bullous disorder most commonly seen in the elderly and manifests as tense blisters on urticarial base, predominantly over flexures, and is associated with pruritus. The diagnosis can be confirmed by histology, direct and indirect immunofluorescence. Several new diagnostic techniques have also been developed. Treatment of BP is based on the extent and rate of progression of the disease. Several topical and systemic anti-inflammatory and immunosuppressive agents have been used with variable results.	en_US
dc.identifier.citation	Khandpur Sujay, Verma Parul. Bullous pemphigoid. Indian Journal of Dermatology, Venereology and Leprology. 2011 Jul-Aug; 77(4): 450-455.	en_US
dc.identifier.uri	https://imsear.searo.who.int/handle/123456789/140882
dc.language.iso	en	en_US
dc.source.uri	https://www.ijdvl.com/article.asp?issn=0378-6323;year=2011;volume=77;issue=4;spage=450;epage=455;aulast=Khandpur	en_US
dc.subject	Bullous pemphigoid	en_US
dc.subject	clinical features	en_US
dc.subject	management	en_US
dc.subject	India	en_US
dc.title	Bullous pemphigoid.	en_US
dc.type	Article	en_US

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