Malar blistering: A diagnostic dilemma

Bullous pemphigoid (BP) is an autoimmune blistering disorder affecting elderly people. It presents as tense blisters on urticarial base and is associated with intense pruritus. It commonly involves lower abdomen, inner or anterior thighs, and flexor forearms. Localized BP limited to certain parts of...

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Veröffentlicht in:Clinical Dermatology Review 2019, Vol.3 (2), p.145-147
Hauptverfasser: Shilpa, Kanathur, Leelavathy, B, Lakshmi, DV, Gorur, Divya
Format: Artikel
Sprache:eng
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Zusammenfassung:Bullous pemphigoid (BP) is an autoimmune blistering disorder affecting elderly people. It presents as tense blisters on urticarial base and is associated with intense pruritus. It commonly involves lower abdomen, inner or anterior thighs, and flexor forearms. Localized BP limited to certain parts of the body has also been described in literature. Both classical and localized BP is diagnosed based on histopathology and immunofluorescence. Corticosteroids remain the main stay of treatment. Here, we describe a case of BP presenting as malar blistering closely mimicking bullous systemic lupus erythematosus.
ISSN:2542-551X
2542-5528
DOI:10.4103/CDR.CDR_24_18