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埃勒斯-当洛综合征的胃肠道受累情况。

Gastrointestinal involvement in the Ehlers-Danlos syndromes.

作者信息

Fikree Asma, Chelimsky Gisela, Collins Heidi, Kovacic Katcha, Aziz Qasim

出版信息

Am J Med Genet C Semin Med Genet. 2017 Mar;175(1):181-187. doi: 10.1002/ajmg.c.31546. Epub 2017 Feb 10.

Abstract

Current evidence suggests that an association exists between non-inflammatory hereditary disorders of connective tissue such as the Ehlers-Danlos syndromes (EDS) and gastrointestinal (GI) symptoms. Patients with EDS can present with both structural problems such as hiatus hernias, visceroptosis, rectoceles, and rectal prolapse as well as functional problems such as disordered gut motility. It has recently been demonstrated that patients with hypermobile EDS (hEDS) present with GI symptoms related to the fore and hind-gut and these patients frequently meet the criteria for functional gastrointestinal disorders such as functional dyspepsia and irritable bowel syndrome. Presence of GI symptoms in EDS patients influences their quality of life. Specific evidence based management guidelines for the management of GI symptoms in EDS patients do not exist and these patients are often treated symptomatically. There is, however, recognition that certain precautions need to be taken for those patients undergoing surgical treatment. Future studies are required to identify the mechanisms that lead to GI symptoms in patients with EDS and more specific treatment guidelines are required. © 2017 Wiley Periodicals, Inc.

摘要

目前的证据表明,诸如埃勒斯-当洛综合征(EDS)等非炎症性遗传性结缔组织疾病与胃肠道(GI)症状之间存在关联。EDS患者可能出现诸如食管裂孔疝、内脏下垂、直肠膨出和直肠脱垂等结构性问题,以及诸如肠道动力紊乱等功能性问题。最近有研究表明,活动度过高型EDS(hEDS)患者会出现与前肠和后肠相关的GI症状,并且这些患者常常符合诸如功能性消化不良和肠易激综合征等功能性胃肠疾病的标准。EDS患者出现GI症状会影响他们的生活质量。目前尚无针对EDS患者GI症状管理的基于具体证据的管理指南,这些患者通常接受对症治疗。然而,人们认识到,对于那些接受手术治疗的患者需要采取某些预防措施。未来需要开展研究以确定导致EDS患者出现GI症状的机制,并且需要更具体的治疗指南。© 2017威利期刊公司

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