首页> 美国卫生研究院文献>Hereditary Cancer in Clinical Practice >High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report
【2h】

High-grade endometrial stromal sarcoma as the initial presentation of an adult patient with Peutz-Jeghers Syndrome: a case report

机译:成人子宫内膜间质肉瘤为Peutz-Jeghers综合征的成年患者的初步表现:一例报告

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 46-year-old female presents with a pelvic mass and is diagnosed as having a high-grade endometrial stromal sarcoma. During surgery, she is noted to have areas of intussusception of the small bowel secondary to large hamartomatous polyps. The patient had a previous history of small bowel obstruction secondary to what had been thought to be hyperplastic polyps but represented hamartomatous polyps on further review. Additional examination revealed the presence of subtle hyperpigmented macules on the fingers leading to a diagnosis of Peutz-Jeghers Syndrome (PJS). The diagnosis was confirmed by the presence of a germ-line STK11 mutation. Immunohistochemistry analysis of the tumor showed decreased expression of STK-11 as compared to one of the patient’s hamartomatous polyps. Next generation sequencing of the tumor specimen failed to demonstrate a “second hit” somatic mutation in STK-11. This case represents the first case of endometrial stromal sarcoma associated with PJS and illustrates the importance of increased awareness of this condition among oncologists. PJS is associated with dysregulation of the mTOR pathway; treatment with an mTOR inhibitor was not effective in this case.Electronic supplementary materialThe online version of this article (doi:10.1186/s13053-015-0027-0) contains supplementary material, which is available to authorized users.
机译:一名46岁的女性表现为盆腔肿块,被诊断为患有高度子宫内膜间质肉瘤。在手术期间,她被发现有继发于大型错构瘤性息肉的小肠套叠区域。该患者先前有小肠梗阻的病史,继发于被认为是增生性息肉的病灶,但在进一步的检查中表现为错构瘤性息肉。进一步检查发现手指上存在色素沉着的细微斑点,可诊断为Peutz-Jeghers综合征(PJS)。通过种系STK11突变的存在证实了诊断。对该肿瘤的免疫组织化学分析显示,与该患者的一个错构瘤息肉之一相比,STK-11的表达降低。肿瘤标本的下一代测序未能证明STK-11中的“第二击”体细胞突变。该病例代表了首例与PJS相关的子宫内膜间质肉瘤,并说明了肿瘤科医生对此病认识的提高的重要性。 PJS与mTOR通路的失调有关。在这种情况下,用mTOR抑制剂治疗无效。电子补充材料本文的在线版本(doi:10.1186 / s13053-015-0027-0)包含补充材料,授权用户可以使用。

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