PDF(Pubmed)
Abstract：
Porokeratosis, a keratinizing disorder of unknown etiology, exhibits an autosomal dominant inheritance pattern or manifests as an isolated acquired dermatosis. This condition can occur at any site on the skin; however, scrotal lesions are extremely rare. Only 18 cases of scrotal lesions were identified through a comprehensive review of the relevant literature. Herein, we present a case of a 19-year-old patient with porokeratosis of the scrotum. Additionally, we provide a summary of the etiologies, clinical manifestations, and histopathology of scrotal porokeratosis, and present differential diagnoses by reviewing the related literature.
摘要：
角化病,一种病因不明的角质化疾病,表现出常染色体显性遗传模式或表现为孤立的获得性皮肤病。这种情况可以发生在皮肤上的任何部位;然而，阴囊病变极为罕见。通过对相关文献的全面回顾，仅确认了18例阴囊病变。在这里，我们介绍一例19岁的阴囊孔角化症患者。此外,我们提供了病因的总结，临床表现，和阴囊孔角化病的组织病理学，并通过回顾相关文献提出鉴别诊断。
