Gelincik Ibrahim
Department of Pathology, Region Education and Research Hospital, Erzurum, Turkey.
Indian J Pathol Microbiol. 2011 Jan-Mar;54(1):150-1. doi: 10.4103/0377-4929.77380.
A 25-year-old woman was seen for a painless subcutaneous mass of 2 years duration. On excisional biopsy, a collapsed cystic structure lined by stratified, ciliated, columnar epithelium was noted. These linning cells did not produce mucin. Immunohistochemical staining for progesterone receptor, estrogen receptor and epithelial membrane antigen was positive, whereas it was negative for carcinoembryonic antigen. Findings were consistent with cutaneous ciliated cyst (CCC). CCCs are rare, predominantly occurring on the lower extremities of young women. Most of them have been regarded as Mullerian remnants. A case of a CCC in the subcutaneous area is reported.
一名25岁女性因无痛性皮下肿物就诊,肿物已存在2年。切除活检时,发现一个塌陷的囊性结构,内衬分层的、有纤毛的柱状上皮。这些内衬细胞不产生黏液。孕激素受体、雌激素受体和上皮膜抗原的免疫组化染色呈阳性,而癌胚抗原染色呈阴性。结果符合皮肤纤毛囊肿(CCC)。CCC罕见,主要发生在年轻女性的下肢。大多数被认为是苗勒管残余物。本文报告一例皮下区域的CCC。