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eISSN: 2084-9893
ISSN: 0033-2526
Dermatology Review/Przegląd Dermatologiczny
Bieżący numer Archiwum Artykuły zaakceptowane O czasopiśmie Zeszyty specjalne Rada naukowa Bazy indeksacyjne Prenumerata Kontakt Zasady publikacji prac Standardy etyczne i procedury
Panel Redakcyjny
Zgłaszanie i recenzowanie prac online
SCImago Journal & Country Rank
5/2024
vol. 111
 
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Opis przypadku

Seborrheic Pemphigoid

Marcelina Kądziela
1
,
Aleksandra Fijałkowska
1
,
Agnieszka Żebrowska
1

  1. Department of Dermatology and Venereology, Medical University of Lodz, Lodz, Poland
Dermatol Rev/Przegl Dermatol 2024, 11, 386-389
Data publikacji online: 2025/02/25
Pełna treść artykułu Pobierz cytowanie
 
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Introduction:
Bullous pemphigoid is an autoimmune blistering disease with a complex etiology. It affects mostly elderly individuals and can be triggered by several factors, including comorbidities, medications, infections and physical factors. The clinical picture is characterized by erythema and urticarial lesions, tense blisters and severe pruritus. Skin lesions are very rarely located in typical seborrheic areas and such a variant is referred to as seborrheic pemphigoid.

Case report:
A 41-year-old female patient was referred to the Department of Dermatology and Venerology with erythematous macules, vesicles and bullae filled with serous fluid or hemorrhagic fluid and distributed on the skin of the face and chest. On direct immunofluorescence, immunoglobulins and complement deposits at the basement membrane zone were found.

Conclusions:
The diagnosis of seborrheic pemphigoid was made. This is a rare disease that should be differentiated from seborrheic dermatitis. Indirect and direct immunofluorescence tests may be helpful in the differential diagnosis.



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