Department of Pathology, UT Southwestern Medical Center, Dallas, TX, USA.
Int J Surg Pathol. 2020 Aug;28(5):569-573. doi: 10.1177/1066896920901764. Epub 2020 Jan 28.
Large cell neuroendocrine carcinoma (LCNEC) of the endometrium is an exceedingly rare histologic subtype of endometrial cancer (0.8%). These tumors are highly aggressive with a propensity for metastasis and have a poor prognosis. Among the 17 cases reported to date, 9 cases were pure large cell neuroendocrine tumors and 8 were collision tumors of LCNEC with endometrial carcinomas (7 endometrioid and 1 serous). In this article, we report a case of collision tumor composed of an endometrial LCNEC and a low-grade endometrial stromal sarcoma (LGESS). The patient was a 48 year-old woman who presented with a large abdominal mass for about 10 years and underwent total hysterectomy, bilateral salpingo-oophorectomy, and tumor debulking. Microscopic evaluation demonstrated an LGESS with extensive osseous metaplasia that penetrated through the myometrium and invaded into pelvic and abdominal cavity, forming a 40.0-cm mass. Cytogenetic analysis of the LGESS revealed an abnormal female karyotype (45, XX) with multiple structural abnormalities. Incidentally, small foci of LCNEC were identified within the endometrium. The LCNEC focally invaded the myometrium with involvement of the endocervix, extensive lymph-vascular space invasion, and metastases to bilateral ovaries. Subsequently, the patient was treated with cisplatin/etoposide chemotherapy and had been doing well for about a year until presenting with recurrence of LCNEC in the abdomen. She passed away a month later due to medical complications. This report reveals an extremely rare endometrial collision tumor with unusual pathologic features and clinical presentations.
子宫内膜的大细胞神经内分泌癌(LCNEC)是一种极为罕见的子宫内膜癌组织学亚型(0.8%)。这些肿瘤具有高度侵袭性,易发生转移,预后不良。迄今为止,已有 17 例报道,其中 9 例为纯大细胞神经内分泌肿瘤,8 例为 LCNEC 与子宫内膜癌的碰撞肿瘤(7 例子宫内膜样癌和 1 例浆液性癌)。本文报道了 1 例由子宫内膜 LCNEC 和低度子宫内膜间质肉瘤(LGESS)组成的碰撞肿瘤。患者为 48 岁女性,因腹部巨大肿块约 10 年就诊,行全子宫切除术、双侧附件切除术和肿瘤减灭术。镜下评估显示广泛骨化生的 LGESS 穿透子宫肌层并侵犯盆腔和腹腔,形成 40.0cm 大肿块。LGESS 的细胞遗传学分析显示异常女性核型(45,XX),存在多种结构异常。偶然发现子宫内膜内有小灶性 LCNEC。LCNEC 局灶性侵犯子宫肌层,累及宫颈,广泛淋巴管血管间隙浸润,双侧卵巢转移。随后,患者接受顺铂/依托泊苷化疗,病情稳定约 1 年,随后腹部 LCNEC 复发。一个月后因医疗并发症去世。本报告揭示了一种具有异常病理特征和临床表现的极为罕见的子宫内膜碰撞肿瘤。