Pemphigoid nodularis

Journal of Cutaneous Medicine and Surgery
Waleed Al-Salhi, Ru'aa Alharithy

Abstract

Pemphigoid nodularis is a rare clinical variant of bullous pemphigoid characterized by overlapping clinical features of both prurigo nodularis lesions and bullous pemphigoid blisters. The condition appears to be more common in females and is often resistant to treatment. To raise awareness of this rare variant of bullous pemphigoid. Case report. Dermatologists should include this variant in differential diagnosis of prurigo nodularis because early recognition can lead to an effective treatment for the prurigo component.

References

Jun 1, 1992·Journal of Cutaneous Pathology·J S RossM M Black
Jul 1, 1981·Journal of the American Academy of Dermatology·C W YungA L Lorincz
Nov 1, 1994·Clinical and Experimental Dermatology·J F BourkeD A Burns
Dec 1, 1993·The British Journal of Dermatology·R GalloA Rebora
Mar 1, 1997·The British Journal of Dermatology·S Cliff, C A Holden
Jan 29, 2000·The British Journal of Dermatology·H FujisawaT Hashimoto
Aug 14, 2002·The British Journal of Dermatology·A M PowellM M Black

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Citations

Jan 27, 2019·Experimental and Therapeutic Medicine·Corina VornicescuLoredana Ungureanu
Sep 29, 2019·Medicines·Christina D KwonShawn G Kwatra

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Methods Mentioned

BETA
biopsy

Related Concepts

Related Feeds

Bullous Pemphigoid

Bullous pemphigoid is a rare immune system disorder and skin condition that causes large, fluid-filled blisters. Bullous pemphigoid commonly affects older adults and appears in areas such as the lower abdomen, upper thighs or armpits. Discover the latest research on bullous pemphigoid here.

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