首页> 美国卫生研究院文献>Oxford Medical Case Reports >Perivascular epithelioid cell tumour and mesonephric adenocarcinoma of the uterine cervix: an unknown co-existence
【2h】

Perivascular epithelioid cell tumour and mesonephric adenocarcinoma of the uterine cervix: an unknown co-existence

机译:子宫颈周围血管上皮样细胞瘤和中肾腺癌:未知的共存

代理获取
本网站仅为用户提供外文OA文献查询和代理获取服务,本网站没有原文。下单后我们将采用程序或人工为您竭诚获取高质量的原文,但由于OA文献来源多样且变更频繁,仍可能出现获取不到、文献不完整或与标题不符等情况,如果获取不到我们将提供退款服务。请知悉。

摘要

A 67-year-old woman with post-menopausal bleeding and a suspicious endocervical mass was referred to gynaecology outpatients’ for diagnosis and management. Cervical punch biopsies taken showed a benign cervical perivascular epithelioid cell tumour (PEComa), with MRI imaging and PET-CT scan indicating a 3–4 cm endocervical tumour with malignant features. The patient underwent radical hysterectomy with lymph node dissection and the surgical specimen histopathology demonstrated a residual benign PEComa and a stage IIB mesonephric adenocarcinoma (MNA) of the cervix. There is no disease recurrence 12 months after surgery. Cervical PEComas are extremely rare tumours of mesenchymal origin deriving from the perivascular epithelioid cells with only 14 cases described so far. Cervical MNAs are rare tumours originating from the remnants of the mesonephric duct of Wolff with only 40 cases reported. Our case adds to the existing literature and highlights the challenges with regard to preoperative diagnosis, treatment and prognosis.
机译:一名67岁的绝经后出血和可疑子宫颈管肿物的妇女被转诊至妇科门诊进行诊断和处理。宫颈穿孔活检显示为良性宫颈血管周上皮样细胞瘤(PEComa),MRI和PET-CT扫描显示3–4 cm宫颈恶性肿瘤。该患者接受了根治性子宫切除术并进行了淋巴结清扫术,并且手术标本的组织病理学表现为残留的良性PEComa和子宫颈的IIB期中肾腺癌(MNA)。手术后12个月没有疾病复发。子宫颈PEComas是间充质来源的极为罕见的肿瘤,起源于血管周上皮样细胞,迄今仅描述了14例。宫颈MNA是罕见的肿瘤,起源于Wolff的中肾管残余,仅报道40例。我们的病例增加了现有文献,并突出了术前诊断,治疗和预后方面的挑战。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
代理获取

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号