异常部位乳头状淋巴管囊腺瘤1例报告

A. Gulanikar, Omkar S. Kulkarni
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引用次数: 0

摘要

1例15岁女性,自幼出现背部病变,偶有出血和渗出,无全身症状。左下背部有多个疣状合并丘疹形成斑块,并有上覆糜烂,暂时诊断为血管角质瘤边缘,并行活检。组织病理学检查结果与乳头状淋巴管囊腺瘤一致。手术切除并用旋转皮瓣闭合。淋巴管囊腺瘤是一种良性的皮肤附件肿瘤,临床表现为多种形态,如疣状丘疹、结节、斑块伴浆液性物质渗出。病变通常见于头部和颈部,但也可发生在四肢,臀部,肛门生殖器区域。它的特征是皮肤表面与毛囊相关的多重内陷,在腔面由立方体上皮到柱状上皮排列,在外面是肌上皮细胞。有乳头状结构和真皮导管成分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Syringocystadenoma Papilliferum at an Unusual Location: a Case Report
A case of 15year old female presented with lesion over back since childhood, with occasional bleeding and oozing from lesion without any associated systemic complaints. There were multiple verrucous coalescing papules forming plaque with overlying erosion present over left lower back- diagnosed provisionally as angiokeratoma circumscriptum and was biopsied. Histopathology revealed findings consistent with Syringocystadenoma papilliferum. Surgical excision was done and closed with rotation flap. Syringocystadenoma is benign cutaneous adnexal tumor presenting clinically with many morphologies such as warty papules, nodules, plaques with oozing of serous material. Lesion is usually seen in head and neck area in most cases however can also occur on extremities, buttocks, anogenital region. It is characterized by multiple invaginations from skin surface in association with hair follicles lined by cuboidal to columnar epithelium on luminal aspect and myoepithelial cells on outside. There is papillary architecture and dermal ductal component.
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