Oh Jin Sol, Bhalla Varun K, Needham Lance, Sharma Suash, Pipkin Walter L, Hatley Robyn M, Howell Charles G
Department of General Surgery, Georgia Regents University, 1120 15th Street, Room BIW 446, Augusta, GA, 30912, USA.
Pediatr Surg Int. 2014 May;30(5):545-8. doi: 10.1007/s00383-013-3363-z. Epub 2013 Aug 4.
A cutaneous ciliated cyst is a rare entity found predominantly in the lower extremities and perineal region of young females. Although initially described by Hess in 1890, the present day term, "cutaneous ciliated cyst," was proposed by Farmer in 1978 and includes a wide array of cyst types. Despite their typical female predominance and location, many have described cutaneous ciliated cysts in males and atypical locations. In addition, Mullerian cysts in the posterior mediastinum and the retroperitoneum have been reported. To date, only 40 cases have been reported in the literature of a Mullerian-type, cutaneous ciliated cyst. Here, we report a case of 13-year-old female with one in the gluteal cleft, initially presenting as a pilonidal cyst. We also discuss the differential diagnosis of pediatric sacrococcygeal lesions and pathogenesis of a Mullerian-type, cutaneous ciliated cyst.
皮肤纤毛囊肿是一种罕见的病变,主要见于年轻女性的下肢和会阴区。尽管1890年赫斯首次对其进行了描述,但“皮肤纤毛囊肿”这一现代术语是1978年由法默提出的,它涵盖了多种囊肿类型。尽管其典型表现为女性居多且好发于特定部位,但也有许多关于男性及非典型部位皮肤纤毛囊肿的报道。此外,后纵隔和腹膜后的苗勒管囊肿也有相关报道。迄今为止,文献中仅报道了40例苗勒管型皮肤纤毛囊肿。在此,我们报告一例13岁女性,其臀沟处有一个囊肿病变,最初表现为藏毛窦。我们还讨论了儿童骶尾部病变的鉴别诊断以及苗勒管型皮肤纤毛囊肿的发病机制。