腹膜透明细胞腺癌：一例报告及文献复习

Shigeta Naoya, Yoshino Kiyoshi, Matsuzaki Shinya, Morii Eiichi, Ueda Yutaka, Kimura Tadashi

Department of Obstetrics and Gynecology, Osaka University Graduate School of Medicine, 2-2 Yamadaoka, Suita 565-0871, Osaka, Japan.

J Ovarian Res. 2014 Oct 2;7:86. doi: 10.1186/s13048-014-0086-2.

Clear cell adenocarcinoma (CCC) is generally thought to originate from ovarian, endometrial, or renal tissue. A CCC of the peritoneum (CCAP) is an extremely rare medical condition and is associated with a poor prognosis. To date, only 10 cases of CCAP have been reported, of which half resulted in death or recurrence within 6 months after initial treatment because CCAP is commonly resistant to multiple drugs. In this report, we present a case of CCAP of the pouch of Douglas coexisting with an endometriosis and we offer a review of the related literature.

透明细胞腺癌（CCC）通常被认为起源于卵巢、子宫内膜或肾脏组织。腹膜透明细胞腺癌（CCAP）是一种极其罕见的病症，预后较差。迄今为止，仅报道了10例CCAP病例，其中半数在初始治疗后6个月内死亡或复发，因为CCAP通常对多种药物耐药。在本报告中，我们呈现了1例Douglas陷凹CCAP合并子宫内膜异位症的病例，并对相关文献进行了综述。