Ting W H, Hsiao S M, Lin H H, Wei M C
Eur J Gynaecol Oncol. 2014;35(1):100-2.
Primary ovarian carcinoid tumors are rare entities, they may appear with other teratomatous components, and can be often being mistaken as part of mature cystic teratomas. Consistent with their rarity and low incidence, imaging clues that could have led to suspicion of this tumor are not well-documented. Herein, the authors present a rare case of primary ovarian carcinoid tumor in a mature cystic teratoma, who initially presented with complaints of abdominal distension for months. Contrast-enhanced computerized tomography (CT) demonstrated a multilobular mass with different density components including fat, soft tissue, and calcification materials, as well as rich vascular supply from the right ovarian vein. Serum tumor markers were within normal limits. Bilateral salpingo-oophorectomy was performed and the pathological diagnosis was mature cystic teratoma with coexisting primary ovarian carcinoid tumor, insular type. The patient has remained well with no residual disease for over one year of follow-up.
原发性卵巢类癌肿瘤是罕见的实体瘤,它们可能与其他畸胎瘤成分同时出现,并且常常被误诊为成熟囊性畸胎瘤的一部分。鉴于其罕见性和低发病率,能够提示怀疑该肿瘤的影像学线索尚无充分记录。在此,作者报告一例罕见的成熟囊性畸胎瘤合并原发性卵巢类癌肿瘤的病例,患者最初因腹胀数月就诊。增强计算机断层扫描(CT)显示一个多叶状肿块,具有不同密度成分,包括脂肪、软组织和钙化物质,并且右卵巢静脉有丰富的血管供应。血清肿瘤标志物在正常范围内。实施了双侧输卵管卵巢切除术,病理诊断为成熟囊性畸胎瘤合并原发性卵巢类癌肿瘤(岛状型)。经过一年多的随访,患者情况良好,无残留疾病。