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食管壁内假性憩室病合并贲门失弛缓症。

Esophageal intramural pseudodiverticulosis associated with achalasia.

作者信息

Dua K S, Stewart E, Arndorfer R, Shaker R

机构信息

Department of Medicine, MCW Dysphagia Institute, Medical College of Wisconsin, Milwaukee, USA.

出版信息

Am J Gastroenterol. 1996 Sep;91(9):1859-60.

PMID:8792718
Abstract

Esophageal intramural pseudodiverticulosis (EIPD) is a rare condition in which multiple small outpouchings are seen in the wall of the esophagus. Although EIPD is typically associated with esophageal narrowing, only a few cases have been described in which it was associated with esophageal dysmotility. We report the case of a 52-yr-old female who presented with dysphagia and who had EIPD protruding from a 5-cm-long concentric distal esophageal stricture, with a markedly dilated upper and middle third of the esophagus. The short segment of the esophagus between the stricture and the lower esophageal sphincter also was dilated. Barium column was held up above a nonrelaxing lower esophageal sphincter that opened after inhalation of amylnitrate. Esophageal manometry confirmed the presence of vigorous achalasia. Although EIPD has been associated with several other conditions, this is the first report of an association with achalasia.

摘要

食管壁内假性憩室病(EIPD)是一种罕见疾病,其特征为在食管壁内可见多个小的憩室样突出。尽管EIPD通常与食管狭窄相关,但仅有少数病例报道其与食管动力障碍有关。我们报告一例52岁女性患者,该患者因吞咽困难就诊,其EIPD从一段5厘米长的同心性食管远端狭窄处突出,食管上、中段明显扩张。狭窄与食管下括约肌之间的短段食管也有扩张。钡剂柱在不松弛的食管下括约肌上方受阻,吸入亚硝酸异戊酯后该括约肌开放。食管测压证实存在强力型贲门失弛缓症。尽管EIPD已与其他多种疾病相关,但这是首例关于其与贲门失弛缓症相关的报道。

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