Al Hawsawi Khalid, Alharazi Amani, Ashary Abeer, Siddique Asmaa
Dermatology Department, King Abdul Aziz Hospital, Makkah, Saudi Arabia.
College of Medicine, Umm Al-Qura University, Makkah, Saudi Arabia.
Case Rep Dermatol. 2019 Feb 14;11(1):36-39. doi: 10.1159/000497054. eCollection 2019 Jan-Apr.
Syringocystadenoma papilliferum is a very rare, benign adnexal tumor that originates from the apocrine sweat glands. Herein, we report a 25-year-old male who presented with a 10-year history of an asymptomatic slowly growing skin lesion on his face. Skin examination revealed a solitary rounded 3 × 3 cm erythematous plaque with central crustation on the right side of his face. Punch skin biopsy was taken from the lesion. The epidermis showed downward papillomatous extensions. The dermis showed multiple epithelial sheets and dilated ducts that were lined by columnar cells. On the basis of the above clinicopathological findings, the diagnosis of syringocystadenoma papilliferum was made. The patient was reassured and referred to a surgeon for surgical excision of the lesion.
乳头状汗管囊腺瘤是一种非常罕见的良性附属器肿瘤，起源于顶泌汗腺。在此，我们报告一名25岁男性，他面部有一个无症状的缓慢生长的皮肤病变，病史长达10年。皮肤检查发现其面部右侧有一个孤立的圆形3×3 cm红斑性斑块，中央有结痂。从病变处取了皮肤穿刺活检。表皮显示向下的乳头状延伸。真皮显示多个上皮细胞层和由柱状细胞衬里的扩张导管。根据上述临床病理表现，诊断为乳头状汗管囊腺瘤。患者得到了安慰，并被转介给外科医生进行病变的手术切除。
