原发性子宫颈癌肉瘤1例报告。

Pub Date : 2022-08-02 eCollection Date: 2022-07-01 DOI:10.1055/s-0042-1744152
Georgios Tsatsaris, Zacharias Fasoulakis, Antonios Koutras, Thomas Ntounis, Athina A Samara, Athanasios Syllaios, Alexandros Diamantis, Maria Kouroupi, Charilaos Stamos, Emmanuel N Kontomanolis
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引用次数: 1

摘要

背景:癌肉瘤是恶性混合性勒氏瘤(MMMT),包含上皮和间质成分。子宫颈癌肉瘤是一种极其罕见的组织病理实体,迄今为止文献报道的病例不到150例。材料与方法一名79岁绝经后女性患者因盆腔肿块及阴道出血转介至我科。宫颈刮除和组织学报告显示恶性肿瘤高细胞组成的两个组成部分;前者是软骨肉瘤,后者是腺癌。免疫组化(IHC)染色证实MMMT的诊断。实施新辅助化疗和放疗,一年后患者行根治性子宫切除术和肿瘤盆腔淋巴结清扫术。术后12个月无病。结论原发性宫颈癌肉瘤是一种极为罕见的双侧肿瘤。术前诊断与适当的免疫化学测试这种罕见的实体是至关重要的决策。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

Primary Cervical Carcinosarcoma: Report of a Rare Case.

Primary Cervical Carcinosarcoma: Report of a Rare Case.

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Primary Cervical Carcinosarcoma: Report of a Rare Case.

Background  Carcinosarcomas are malignant mixed Müllerian tumors (MMMT), containing both epithelial and mesenchymal components. Carcinosarcomas of the uterine cervix comprise an extremely rare histopathological entity, with less than 150 cases reported in the literature to date. Materials and Methods  A 79-year-old postmenopausal female patient was referred to our gynecological department due to a pelvic mass and vaginal bleeding. A cervical curettage was performed and the histological report revealed a malignant neoplasm with high cellularity consisting of two components; the first was a chondrosarcoma and the latter a adenocarcinoma. A diagnosis of MMMT was confirmed through immunohistochemical (IHC) staining. Neoadjuvant chemotherapy and radiotherapy were implemented, and a year later the patient underwent a radical hysterectomy and oncological pelvic lymph node dissection. She remains disease-free 12 months postoperatively. Conclusion  Primary cervical carcinosarcomas are extremely rare tumors demonstrating a bipartite profile. Preoperative diagnosis with appropriate immunochemistry testing of this rare entity is crucial to decision making.

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