首页> 外文期刊>Postgraduate Medical Journal >Fulminant ischaemic colitis with atypical clinical features complicating sickle cell disease.
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Fulminant ischaemic colitis with atypical clinical features complicating sickle cell disease.

机译:具有典型临床特征的镰状缺血性结肠炎使镰状细胞病复杂化。

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摘要

Clinically significant ischaemic bowel injury is an exceedingly rare complication of sickle cell disease. It manifests as acute surgical abdomen and may respond to conservative treatment. An unusual fatal case of ischaemic colitis with minimal abdominal findings in a young male during a sickle cell vaso-occlusive pain crisis is described. This case demonstrates that an acute surgical abdomen should be considered in such patients who fail to respond to conservative management as untreated this condition may be fatal.
机译:临床上严重的缺血性肠损伤是镰状细胞病的极为罕见的并发症。它表现为急性手术腹部,可能对保守治疗有反应。描述了在镰状细胞血管闭塞性疼痛危机期间,一名年轻男性的腹部脂肪异常少见的缺血性结肠炎的致命病例。该病例表明,对保守治疗无效的患者应考虑急性手术腹部,因为未经治疗可能会致命。

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