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原发性宫颈癌肉瘤:1例罕见病例报告。

Primary Cervical Carcinosarcoma: Report of a Rare Case.

作者信息

Tsatsaris Georgios, Fasoulakis Zacharias, Koutras Antonios, Ntounis Thomas, Samara Athina A, Syllaios Athanasios, Diamantis Alexandros, Kouroupi Maria, Stamos Charilaos, Kontomanolis Emmanuel N

机构信息

Department of Obstetrics and Gynecology, Democritus University of Thrace, Dragana, Alexandroupolis, Greece.

Department of Obstetrics and Gynecology, National and Kapodistrian University of Athens, General Hospital of Athens "ALEXANDRA," Athens, Greece.

出版信息

Surg J (N Y). 2022 Aug 2;8(3):e174-e178. doi: 10.1055/s-0042-1744152. eCollection 2022 Jul.

DOI:10.1055/s-0042-1744152
PMID:35928548
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC9345680/
Abstract

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.  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.  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.

摘要

癌肉瘤是恶性混合性苗勒管肿瘤(MMMT),包含上皮和间充质成分。宫颈癌肉瘤是一种极其罕见的组织病理学实体,迄今为止文献报道的病例不足150例。一名79岁绝经后女性患者因盆腔肿块和阴道出血转诊至我院妇科。进行了宫颈刮除术,组织学报告显示为一种细胞丰富的恶性肿瘤,由两种成分组成;第一种是软骨肉瘤,第二种是腺癌。通过免疫组织化学(IHC)染色确诊为MMMT。实施了新辅助化疗和放疗,一年后患者接受了根治性子宫切除术和肿瘤盆腔淋巴结清扫术。术后12个月她仍无疾病。原发性宫颈肉瘤是极其罕见的肿瘤,具有双重特征。对这种罕见实体进行适当的免疫化学检测以进行术前诊断对决策至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7cc/9345680/215c41a350c6/10-1055-s-0042-1744152-i2100201cr-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7cc/9345680/53c457aa1bda/10-1055-s-0042-1744152-i2100201cr-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7cc/9345680/215c41a350c6/10-1055-s-0042-1744152-i2100201cr-2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7cc/9345680/53c457aa1bda/10-1055-s-0042-1744152-i2100201cr-1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d7cc/9345680/215c41a350c6/10-1055-s-0042-1744152-i2100201cr-2.jpg

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本文引用的文献

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The Role of Postoperative Radiotherapy for Carcinosarcoma of the Uterus.术后放疗在子宫癌肉瘤中的作用
Cancers (Basel). 2020 Nov 30;12(12):3573. doi: 10.3390/cancers12123573.
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Uterine carcinosarcomas (malignant mixed müllerian tumours): a review with special emphasis on the controversies in management.子宫癌肉瘤(恶性混合性苗勒管肿瘤):一篇特别强调管理争议的综述
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