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[弥漫浸润性贲门癌所致继发性贲门失弛缓症]

[Secondary achalasia caused by diffuse infiltrating cardial cancer].

作者信息

Wenzl E, Starlinger M, Feil W, Stacher G, Schiessel R

机构信息

I. Chirurgische Universitätsklinik, Wien.

出版信息

Chirurg. 1988 Aug;59(8):536-40.

PMID:3215064
Abstract

Malignant tumors, especially gastric adenocarcinomas infiltrating into the submucosa of the esophagus, can result in a clinical syndrome termed secondary or pseudo-achalasia that mimicks idiopathic primary achalasia. History, symptoms, radiology, esophago-gastroscopy with biopsy, and esophageal manometry do not discriminate secondary from primary achalasia at initial evaluation. The difficulty in establishing the diagnosis is demonstrated on the case of a 57-year old man presenting with dysphagia, vomiting, and weight loss. Fluoroscopically, the esophagus was moderately dilated and bird-beaked. The patient underwent two gastroesophagoscopies, in the second of which the endoscope could not be passed through the esophagogastric junction. Esophageal manometry revealed an only partial relaxation of the lower esophageal sphincter upon swallowing and nonpropulsive, repetitive contractions in the esophageal body, compatible with the diagnosis "vigorous achalasia". After two mechanic dilatations, a myotomy of the sphincter seemed indicated. At operation, a cardiac carcinoma infiltrating submucosally into the esophagus was found. The recognition of secondary achalasia is difficult, and signs such as older age, brief duration of symptoms, marked weight loss and the presence of vigorous achalasia, relatively rare in primary achalasia, are unspecific. Hence, in all instances in which secondary achalasia cannot be ruled out, it seems advisable to perform an explorative laparotomy with eventual sphinctermyotomy as primary therapeutic intervention instead of a mechanic dilatation, which potentially further obscures the underlying disease. To enable the recognition of undetected secondary achalasia, all patients with achalasia should be followed up thoroughly.

摘要

恶性肿瘤,尤其是浸润至食管黏膜下层的胃腺癌,可导致一种称为继发性或假性贲门失弛缓症的临床综合征,其酷似特发性原发性贲门失弛缓症。在初始评估时,病史、症状、放射学检查、食管胃镜检查及活检以及食管测压均无法区分继发性与原发性贲门失弛缓症。一名57岁男性患者出现吞咽困难、呕吐和体重减轻,这一病例体现了诊断的困难。透视检查显示食管中度扩张且呈鸟嘴状。该患者接受了两次食管胃镜检查,第二次检查时内镜无法通过食管胃交界处。食管测压显示吞咽时食管下括约肌仅部分松弛,食管体部出现非推进性、重复性收缩,符合“强力型贲门失弛缓症”的诊断。经过两次机械扩张后,似乎需要对括约肌进行肌切开术。手术时发现了一例浸润至食管黏膜下层的贲门癌。继发性贲门失弛缓症的识别较为困难,诸如年龄较大、症状持续时间短、体重显著减轻以及存在强力型贲门失弛缓症等体征,在原发性贲门失弛缓症中相对少见且缺乏特异性。因此,在所有无法排除继发性贲门失弛缓症的情况下,作为主要治疗干预措施,进行探索性剖腹手术并最终行括约肌肌切开术似乎比机械扩张更为可取,因为机械扩张可能会进一步掩盖潜在疾病。为了能够识别未被发现的继发性贲门失弛缓症,所有贲门失弛缓症患者均应进行全面随访。

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