Steatocystoma multiplex suppurativa: case report of a rare condition
An. bras. dermatol
; 91(5,supl.1): 51-53, Sept.-Oct. 2016. graf
Article
ي En
| LILACS
| ID: biblio-837961
المكتبة المسؤولة:
BR1.1
ABSTRACT
Abstract Steatocystoma multiplex is a rare genetic disorder characterized by the presence of hamartomatous malformations at the junction of the pilosebaceous duct. It consists of encapsulated cystic lesions in the dermis, with adjacent sebaceous gland. When associated with inflammation, resembling hidradenitis, it is called steatocystoma multiplex suppurativa, a condition rarely reported. This is the first case of steatocystoma multiplex suppurativa reported in the Brazilian literature. Female patient, 23 years old, with papular and nodular cystic lesions that started in the armpits and groin, later spreading to the trunk, lower limbs, anticubital fossa, face and scalp. The presence of papular-nodular lesions associated with disseminated hidradenitis-like lesions in flexural areas and the histopathological diagnosis of steatocystoma defined the diagnosis of steatocystoma multiplex suppurativa.
Key words
النص الكامل:
1
الفهرس:
LILACS
الموضوع الرئيسي:
Steatocystoma Multiplex
نوع الدراسة:
Diagnostic_studies
المحددات:
Female
/
Humans
اللغة:
En
مجلة:
An. bras. dermatol
موضوع المجلة:
DERMATOLOGIA
السنة:
2016
نوع:
Article