Achalasia: The Current Clinical Dilemma and Possible Pathogenesis.

IF 4.3 3区 材料科学 Q1 ENGINEERING, ELECTRICAL & ELECTRONIC
Xingyu Jia, Songfeng Chen, Qianjun Zhuang, Niandi Tan, Mengyu Zhang, Yi Cui, Jinhui Wang, Xiangbin Xing, Yinglian Xiao
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引用次数: 2

Abstract

Achalasia is a primary esophageal motility disorder manifested by dysphagia and chest pain that impair patients' quality of life, and it also leads to chronic esophageal inflammation by food retention and increases the risk of esophageal cancer. Although achalasia has long been reported, the epidemiology, diagnosis and treatment of achalasia are not fully understood. The current clinical dilemma of achalasia is mainly due to its unclear pathogenesis. In this paper, epidemiology, diagnosis treatment, as well as possible pathogenesis of achalasia will be reviewed and summarized. The proposed hypothesis on the pathogenesis of achalasia is that genetically susceptible populations potentially have a higher risk of infection with viruses, triggering autoimmune and inflammation responses to inhibitory neurons in lower esophageal sphincter.

Abstract Image

失弛缓症:目前的临床困境和可能的发病机制。
贲门失弛缓症是一种原发性食管运动障碍,表现为吞咽困难和胸痛,影响患者的生活质量,并可通过食物潴留引起慢性食管炎症,增加食管癌的发生风险。虽然贲门失弛缓症早有报道,但其流行病学、诊断和治疗尚不完全清楚。目前贲门失弛缓症的临床困境主要是由于其发病机制不明确。本文就失弛缓症的流行病学、诊断治疗及可能的发病机制作一综述。关于贲门失弛缓症发病机制的假设是,遗传易感人群感染病毒的风险可能更高,从而引发对食管下括约肌抑制神经元的自身免疫和炎症反应。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
CiteScore
7.20
自引率
4.30%
发文量
567
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