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盲肠表皮样囊肿:一例报告

Epidermoid cyst of the cecum: a case report.

作者信息

Demır Hale, Aydoğan Begüm, Şahın Hayrettin, Öcal Pelin, Ilvan Şennur

机构信息

İstanbul University, Cerrahpaşa School Of Medicine, Department of Pathology, İstanbul, Turkey.

出版信息

Turk J Gastroenterol. 2012 Aug;23(4):406-9. doi: 10.4318/tjg.2012.0378.

Abstract

Pure, benign epidermoid cysts of the abdominal viscera are rare. There have been only six reports of epidermoid cysts of the cecum in the literature. A 31-year-old female with a previous cesarean delivery was admitted to our hospital with inguinal pain. After admission to the hospital, she was operated with the initial diagnosis of adnexal mass. During the operation, no adnexal pathology was identified. A heterogeneous mass originated from the posterior surface of the cecum was observed. It had no connection with the lumen. The mass was then removed with dissection. Macroscopically, the mass was 9x7 cm in diameter and wall thickness was 0.1 cm. The inner and outer surfaces were smooth. It was filled with a dense yellow, thick-fatty material with no tooth, hair, bone, or calcification areas. On microscopic examination, the inner lining was composed of mature keratinized stratified squamous epithelium with a granular layer. In view of the later findings, the case was reported as epidermoid cyst of the cecum. Although epidermoid cysts are rarely seen in visceral organs, this case is the seventh case of cecum-originated epidermoid cyst that has been reported in the literature. The histogenesis of epidermoid cyst is unknown. These cysts are generally accepted to be sequestration cysts that may be either congenital or acquired. Acquired epidermoid cysts are believed to be traumatic or iatrogenic. The cesarean delivery may have been a cause of this condition in the present case. On ultrasonographic examination, these cysts can be misdiagnosed as ovarian cysts.

摘要

腹腔脏器的单纯性、良性表皮样囊肿较为罕见。文献中仅有6例关于盲肠表皮样囊肿的报道。一名有剖宫产史的31岁女性因腹股沟疼痛入院。入院后,她接受了手术,初步诊断为附件肿物。手术过程中,未发现附件病变。观察到一个起源于盲肠后表面的不均质肿物。它与肠腔无连接。随后将肿物切除。大体上,肿物直径为9×7厘米,壁厚0.1厘米。内外表面光滑。肿物内充满致密的黄色、厚脂肪样物质,无牙齿、毛发、骨骼或钙化区域。显微镜检查显示,内衬由具有颗粒层的成熟角化复层鳞状上皮组成。鉴于后续检查结果,该病例报告为盲肠表皮样囊肿。尽管表皮样囊肿在内脏器官中很少见,但该病例是文献报道的第7例起源于盲肠的表皮样囊肿。表皮样囊肿的组织发生尚不清楚。这些囊肿通常被认为是隔离囊肿,可能是先天性或后天性的。后天性表皮样囊肿被认为是创伤性或医源性的。在本病例中,剖宫产可能是导致这种情况的一个原因。超声检查时,这些囊肿可能被误诊为卵巢囊肿。

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