伴有局灶性肉瘤分化的子宫体中肾样腺癌1例。

Fujita Medical Journal Pub Date : 2025-02-01 Epub Date: 2024-10-31 DOI:10.20407/fmj.2024-017
Serika Kanao, Makoto Urano, Kazuhisa Fujita, Fumi Utsumi, Kazuhiro Sugihara, Kiyosumi Shibata
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引用次数: 0

摘要

子宫体中肾样腺癌于2016年首次报道,并于2020年作为新项目加入世界卫生组织第5版分类。它约占子宫体癌患者的1%,是罕见的。这种癌的组织学不同,使病理诊断困难。与其他组织学类型的子宫体癌相比,诊断是在晚期进行的,据报道预后差,恶性程度高。此外,很少有关于子宫体中肾样腺癌合并肉瘤的病例报道。在本研究中,我们报告了一位患者,在诊断为宫颈癌的情况下进行了术前化疗,但手术后切除的标本被诊断为子宫体的肉瘤成分混合介肾样腺癌。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mesonephric-like adenocarcinoma of the uterine corpus with focal sarcomatous differentiation: A case report.

Mesonephric-like adenocarcinoma of the uterine corpus was first reported in 2016, and added as a new item to the 5th edition of the WHO classification in 2020. It accounts for approximately 1% of patients with uterine corpus cancer, being rare. The histology of this carcinoma varies, making pathological diagnosis difficult. A diagnosis is made at an advanced stage in comparison with other histological types of uterine corpus cancer, and the prognosis is reportedly poor with high-level malignancy. In addition, there are few case reports of mesonephric-like adenocarcinoma of the uterine corpus with sarcoma. In this study, we report a patient in whom preoperative chemotherapy was performed under a diagnosis of cervical carcinoma, but the resected specimen led to a diagnosis of sarcomatous component-mixed mesonephric-like adenocarcinoma of the uterine corpus after surgery.

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