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子宫内膜异位症与 13 种非妇科合并症共存:全外显子组测序的突变分析。

Co-existence of endometriosis with 13 non-gynecological co-morbidities: Mutation analysis by whole exome sequencing.

机构信息

3rd Department of Obstetrics and Gynecology, Aristotle University of Thessaloniki, Thessaloniki 54124, Greece.

Section of Molecular Pathology and Human Genetics, Department of Internal Medicine, School of Medicine, University of Crete, Heraklion 71003, Greece.

出版信息

Mol Med Rep. 2018 Dec;18(6):5053-5057. doi: 10.3892/mmr.2018.9521. Epub 2018 Oct 1.

Abstract

Endometriosis is an enigmatic condition with an unknown etiology and poorly understood pathogenesis and women with endometriosis represent a high-risk population group for a large category of chronic conditions. The study focused on a 67-year-old woman who presented with a 40-year history of familial endometriosis associated with various non-gynecological co-morbidities, thus representing a unique case from a cohort of 1,000 patients with endometriosis. Her family history included infertile members suffering from endometriosis. Thirteen non-gynecological co-morbidities were documented throughout the years, including five autoimmune diseases (i.e., systemic lupus erythematosus, ankylosing spondylitis, multiple sclerosis, bronchial asthma and Crohn's disease), urinary bladder diverticulum, osteoporosis, multinodular goiter, cardiovascular diseases, gastroesophageal reflux disease, malignant tumor of urinary bladder, Barrett's esophagus and bilateral cataract. In order to understand the potential role of gene mutations in the development of all those co-morbidities, whole exome sequencing was performed and the presence of various disease-associated, potentially causal missense variants, were observed. These findings are in accordance with the previously suggested common underlying etiologic pathway for some, but not all, autoimmune disorders. This unusual case provides novel insights demonstrating that endometriosis can coexist with various chronic autoimmune diseases and other conditions, including non-gynecological malignancies, which possibly share a common genetic cause, a fact that should be taken into consideration seriously by clinicians.

摘要

子宫内膜异位症是一种病因不明、发病机制尚不清楚的神秘疾病,患有子宫内膜异位症的女性是一大类慢性疾病的高危人群。本研究聚焦于一位 67 岁的女性,她有 40 年的家族性子宫内膜异位症病史,同时伴有多种非妇科合并症,因此代表了 1000 名子宫内膜异位症患者队列中的一个独特病例。她的家族史包括不孕的子宫内膜异位症患者。多年来共记录了 13 种非妇科合并症,包括 5 种自身免疫性疾病(即系统性红斑狼疮、强直性脊柱炎、多发性硬化症、支气管哮喘和克罗恩病)、膀胱憩室、骨质疏松症、多结节性甲状腺肿、心血管疾病、胃食管反流病、膀胱癌恶性肿瘤、巴雷特食管和双侧白内障。为了了解基因突变在所有这些合并症发展中的潜在作用,进行了全外显子组测序,并观察到了各种与疾病相关的、潜在的致病错义变体的存在。这些发现与之前提出的某些(但不是全部)自身免疫性疾病的共同潜在病因途径一致。这个不寻常的病例提供了新的见解,表明子宫内膜异位症可以与各种慢性自身免疫性疾病和其他疾病共存,包括非妇科恶性肿瘤,这些疾病可能有共同的遗传原因,这一事实应引起临床医生的高度重视。

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