Intradermal Syringocystadenoma Papilliferum on the Popliteal Fossa: A Rare Dermal Variant in an Atypical Location.

Rhode Island medical journal (2013) Pub Date : 2024-07-01
Mohamed Omer, Sean Na, Deep Joshipura, Leslie Robinson-Bostom
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Abstract

Syringocystadenoma papilliferum (SCAP) is a benign adnexal tumor commonly found on the scalp and face, and often associated with nevus sebaceous, with about half of cases appearing in early childhood. SCAP exhibits cystic invaginations with papillary structures and a double-layered glandular epithelium linked to the epidermal surface and stromal plasma cells. We are reporting a rare instance of intradermal SCAP in a 55-year-old male. He sought evaluation for a long-standing asymptomatic dark-pink papule in his left popliteal fossa, measuring 0.7 x 0.5 x 0.4 cm. A shave biopsy revealed papillary dermal fibrosis, glandular epithelium with apocrine secretion, and papillary projections without an epidermal connection. Infundibulofollicular keratinization was observed, along with stromal plasma cells. The patient chose local excision as the treatment option. This case highlights the rarity of intradermal SCAP, especially in the left popliteal fossa, with only one other reported case in the literature.

腘窝皮内乳头状星状囊腺瘤:位置不典型的罕见真皮变异瘤
乳头状星形囊腺瘤(SCAP)是一种良性附件肿瘤,常见于头皮和面部,常伴有皮脂腺痣,约半数病例出现在幼儿期。SCAP表现为具有乳头状结构的囊性浸润,以及与表皮表面和基质浆细胞相连的双层腺上皮。我们报告了一名 55 岁男性皮内 SCAP 的罕见病例。他因左侧腘窝长期无症状的深粉红色丘疹寻求评估,丘疹大小为 0.7 x 0.5 x 0.4 厘米。刮片活检显示真皮乳头状纤维化,腺上皮有分泌物,乳头状突起无表皮连接。还观察到毛囊下角化以及基质浆细胞。患者选择了局部切除作为治疗方案。该病例凸显了皮内 SCAP 的罕见性,尤其是在左侧腘窝,文献中仅有一例报道。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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