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马洛里-魏斯综合征。23例病例回顾并特别提及凝血缺陷。

The Mallory-Weiss syndrome. A review of 23 cases with special reference to coagulation defects.

作者信息

Hellers G, Ewerth S, Ihre T, Lahnborg G

出版信息

Acta Chir Scand Suppl. 1978;482:9-11.

PMID:278441
Abstract

The Mallory-Weiss syndrome is defined as bleeding from longitudinal tears in the gastro-oesophageal junction. The characteristic history consists of repeated vomiting followed by sudden haematemesis. During the past 4 1/2 years, 23 patients, 17 males and 6 females with the diagnosis of Mallory-Weiss syndrome were treated in our institution. An aetiological factor has been sought for. In a review of the case-records, we discovered that many patients had coagulation defects on admission. This was verified with extended coagulation tests at later follow-up. It is proposed that non-bleeding lacerations in the cardiac orifice in conjunction with vomiting is a common occurence, and that the Mallory-Weiss syndrome may be regarded as a complication occuring predominantly in patients with some coagulation defect.

摘要

马洛里-魏斯综合征的定义为胃食管交界处纵向撕裂导致的出血。其典型病史为反复呕吐后突然呕血。在过去4年半的时间里,我院共收治了23例诊断为马洛里-魏斯综合征的患者,其中男性17例,女性6例。我们一直在寻找病因。在回顾病例记录时,我们发现许多患者入院时存在凝血功能缺陷。这在随后的随访中通过延长凝血试验得到了证实。有人提出,贲门处无出血的撕裂伤合并呕吐是一种常见现象,而马洛里-魏斯综合征可被视为主要发生在某些凝血功能缺陷患者中的一种并发症。

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