Gutierrez Villarreal Ilse Marilu, Ancona Castro Circe, Cano Lizarraga Ivan E, Ceballos-Pérez Monica, Cantu Fonseca Grecia Mariana, Gómez López Diego E, Saenz de Leon Carlos S
Dermatology, Institute for Security and Social Services for State Workers (ISSSTE) Monterrey Regional Hospital, Monterrey, MEX.
Internal Medicine, Regional Hospital of High Specialty of the Yucatan Peninsula, Mérida, MEX.
Cureus. 2025 Jun 9;17(6):e85647. doi: 10.7759/cureus.85647. eCollection 2025 Jun.
Disseminated familial comedones without dyskeratosis (DFCWD) is a rare autosomal dominant genodermatosis characterized by widespread comedonal eruptions, predominantly affecting the trunk and face, in the absence of histopathological features such as dyskeratosis or acantholysis. While it exhibits clinical overlap with other entities within the spectrum of familial comedonal disorders, its unique histological features and inheritance pattern support its classification as a distinct clinical entity. Due to the limited number of reported cases, its phenotypic spectrum, natural history, and underlying molecular mechanisms remain poorly understood.
播散性家族性粉刺无角化不良(DFCWD)是一种罕见的常染色体显性遗传性皮肤病,其特征为广泛的粉刺样皮疹,主要累及躯干和面部,且不存在角化不良或棘层松解等组织病理学特征。虽然它与家族性粉刺性疾病谱中的其他疾病存在临床重叠,但其独特的组织学特征和遗传模式支持将其分类为一种独特的临床实体。由于报告的病例数量有限,其表型谱、自然病史和潜在分子机制仍知之甚少。