贲门失弛缓症1例报告及简要回顾

Sameeksha Mishra, D. Bhojani, S. Vaidya
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引用次数: 0

摘要

贲门失弛缓症(Achalasia贲门失弛缓症,AC)是一种罕见的食道运动障碍,它是由神经元变性引起的,这种变性是不可逆的。治疗主要是姑息性的,目前还没有完全治愈的治疗方法。这方面的诊断和治疗主要由于高分辨率测压和经口内窥镜肌切开术(Peroral内镜肌切开术,POEM)而得到加强。正如我们所提到的,高分辨率测压使贲门失弛缓症类型的表征更容易,它也具有重要的治疗作用。贲门失弛缓症必须对每位患者进行单独治疗,充气球囊扩张、POEM或Heller肌切开术的作用需要重新考虑。在我们的病例报告和简要回顾中,我们讨论了诊断基于opd的患者的主要方面和贲门失弛缓症的简要回顾。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Achalasia cardia: A Case Report and a Brief Review
Achalasia cardia (AC) is one of the rarely seen disorders of esophagus motility which happens as a result of degeneration of neurons which is irreversible. Treatment is mainly of palliative nature, and no complete curative treatment is available as of now. The diagnostics and therapeutics in this direction has strengthened mainly due to high-resolution manometry and per-oral endoscopic myotomy, referred to as Peroral endoscopic myotomy (POEM).The characterization of type of achalasia cardia is made easier by high-resolution manometry as we have mentioned, which also has an important therapeutic role. Achalasia has to be managed for each patient individually, and the role of pneumatic balloon dilatation, POEM, or Heller’s myotomy needs to be reconsidered. In our case report and brief review, we discussed the main aspects of diagnosing an OPD-based patient and a brief review of achalasia cardia.
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