Department of Pathology, University of Iowa Hospitals and Clinics, Iowa City, Iowa.
Int J Gynecol Pathol. 2021 May 1;40(3):301-304. doi: 10.1097/PGP.0000000000000675.
Primary ovarian carcinoid tumors are uncommon neoplasms that typically arise in the context of a mature cystic teratoma. Pure primary ovarian carcinoid tumors (PPOCTs) are rare and present as a solid ovarian mass in which, by definition, elements of an associated teratoma or other neoplasm are absent. We report a case of a middle-aged woman who presented with abdominal distension. Computed tomography identified a 20 cm abdominopelvic mass. The patient underwent exploratory laparotomy, hysterectomy, and bilateral salpingo-oophorectomy. A large, solid, yellow-tan ovarian mass was resected and diagnosed as a PPOCT. Para-aortic lymph node metastases were identified. This case highlights the gross and microscopic findings characteristic of PPOCTs. In addition, the large number of differential considerations for an insular PPOCT at intraoperative evaluation are discussed.
原发性卵巢类癌肿瘤是不常见的肿瘤,通常在成熟囊性畸胎瘤的背景下发生。纯原发性卵巢类癌肿瘤(PPOCT)很少见,表现为实性卵巢肿块,根据定义,不存在相关畸胎瘤或其他肿瘤的成分。我们报告了一例中年女性,因腹胀就诊。计算机断层扫描发现 20cm 的腹盆腔肿块。患者接受了剖腹探查术、子宫切除术和双侧输卵管卵巢切除术。切除了一个大的实性、黄棕色卵巢肿块,诊断为 PPOCT。发现了腹主动脉旁淋巴结转移。本病例强调了 PPOCT 的大体和显微镜特征。此外,还讨论了在术中评估时对于岛状 PPOCT 的大量鉴别考虑因素。