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[罕见的暴发性食管酸烧伤]

[Rare occurrence of fulminant acid burn of the esophagus].

作者信息

Knebel C, Bumm R, Becker K, Burian M, Siewert J R

机构信息

Chirurgische Klinik der TU München, Klinikum rechts der Isar, Ismaninger Strasse 22, 81675, München, Deutschland.

出版信息

Chirurg. 2008 Aug;79(8):765-70. doi: 10.1007/s00104-007-1398-1.

Abstract

Peptic ulcer due to Zollinger-Ellison syndrome is a rare entity. In this case report a 55-year-old man had a medical history of esophageal reflux, vomiting, and diarrhea for 10 years. Despite continuous medication with a proton pump inhibitor, no complete recovery from symptoms was achieved. A diagnosis of gastrinoma was at first not considered. After discontinuation of the proton pump inhibitor for only a few days, the strong stimulation of the gastrinoma led to fulminant hydrochloric acid burn of the distal esophagus with iatrogenic or spontaneous perforation at the esophagogastral junction. We describe the operative treatment as a two-stage reconstruction with colon interposition and resection of the primary tumor in the duodenum.

摘要

佐林格-埃利森综合征所致消化性溃疡是一种罕见病症。在本病例报告中,一名55岁男性有10年的食管反流、呕吐和腹泻病史。尽管持续使用质子泵抑制剂治疗,但症状并未完全缓解。起初未考虑胃泌素瘤的诊断。在停用质子泵抑制剂仅几天后,胃泌素瘤的强烈刺激导致食管远端暴发性盐酸灼伤,并在食管胃交界处发生医源性或自发性穿孔。我们描述了手术治疗方法为分两阶段进行结肠间置术并切除十二指肠原发性肿瘤。

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