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子宫内膜小细胞神经内分泌癌与腹腔镜分期:1例临床病理研究及文献简要回顾

Small cell neuroendocrine carcinoma of the endometrium and laparoscopic staging: a clinicopathologic study of a case and a brief review of the literature.

作者信息

Bige O, Saatli B, Secil M, Koyuncuoglu M, Saygili U

机构信息

Department of Obstetrics and Gynecology, Gynecologic Oncology Group, Dokuz Eylul University School of Medicine, Izmir, Turkey.

出版信息

Int J Gynecol Cancer. 2008 Jul-Aug;18(4):838-43. doi: 10.1111/j.1525-1438.2007.01059.x. Epub 2007 Sep 14.

DOI:10.1111/j.1525-1438.2007.01059.x
PMID:17868342
Abstract

Small cell neuroendocrine (NE) carcinoma is one of the most aggressive tumors that arise in the female genital tract. Small cell carcinoma of the endometrium (SCCE) is an extremely rare disease. Because of its rarity, the only clinical reports are limited to case studies, and therefore, clinical behavior and optimal treatment modalities are not well defined. To the best of our knowledge, we present the first case of SCCE staged by laparoscopic approach. A 54-year-old parous woman admitted with intermittent vaginal spotting. On physical examination, she had a 4- x 3-cm mass fungating out of the cervical os. Magnetic resonance imaging showed an endometrial mass of 25 x 30 x 50 mm in dimensions, invading less than 50% of the depth of the myometrium at the uterine fundus. Pathologic examination revealed undifferentiated malign NE tumor of endometrium of small cell type. The patient underwent laparoscopic hysterectomy, bilateral salpingo-oophorectomy, and laparoscopic pelvic and para-aortic lymphadenectomy. The disease was surgically staged as IB. Histologically, tumor cells were monotone, with scanty, ill-defined cytoplasm and hyperchromatic nuclei. Immunohistochemically, tumor showed positive immunoreactivity for P16, neuron-specific enolase, and synaptophysin. She underwent pelvic external radiation and brachytherapy postoperatively. Patient has no evidence of disease after 26 months of follow-up. Small cell NE carcinoma of the endometrium is an extremely rare and aggressive disease. With the availability of skilled endoscopic surgeons, laparoscopic management of women, even with SCCE in early stage, can be a feasible option.

摘要

小细胞神经内分泌(NE)癌是女性生殖道中最具侵袭性的肿瘤之一。子宫内膜小细胞癌(SCCE)是一种极其罕见的疾病。由于其罕见性,唯一的临床报告仅限于病例研究,因此,临床行为和最佳治疗方式尚未明确界定。据我们所知,我们报告了首例通过腹腔镜方法分期的SCCE病例。一名54岁经产妇因间歇性阴道点滴出血入院。体格检查时,可见宫颈口有一个4×3厘米的肿物呈蕈状突出。磁共振成像显示子宫内膜肿物大小为25×30×50毫米,侵犯子宫底部肌层深度不到50%。病理检查显示为小细胞型子宫内膜未分化恶性NE肿瘤。患者接受了腹腔镜子宫切除术、双侧输卵管卵巢切除术以及腹腔镜盆腔和腹主动脉旁淋巴结清扫术。该疾病手术分期为IB期。组织学上,肿瘤细胞单一,细胞质稀少、界限不清,细胞核深染。免疫组化显示,肿瘤对P16、神经元特异性烯醇化酶和突触素呈阳性免疫反应。她术后接受了盆腔外照射和近距离放疗。随访26个月后,患者无疾病迹象。子宫内膜小细胞NE癌是一种极其罕见且具有侵袭性的疾病。随着熟练的内镜外科医生的出现,即使是早期SCCE的女性患者,腹腔镜治疗也可能是一种可行的选择。

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