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Intestinal ischaemia associated with phaeochromocytoma.

机译:肠缺血与嗜铬细胞瘤有关。

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摘要

The present case report describes a patient with an adrenal phaeochromocytoma who presented with infarction of the small intestine. The clinical features, diagnosis and treatment of this case are described. Despite excision of the tumour and necrotic intestine, this patient died in the postoperative period from overwhelming sepsis and multi-organ failure. Special reference is made to the delayed effects of established intestinal ischaemia on immune function and it is suggested that this was major contributory factor to the fatal outcome in the present case. The onset of gastro-intestinal symptoms in patients with phaeochromocytoma should suggest the possibility of imminent gut ischaemia and indicate the necessity for prompt excision of the tumour.
机译:本病例报告描述了患有肾上腺嗜铬细胞瘤的患者,其表现为小肠梗塞。描述了这种情况的临床特征,诊断和治疗。尽管切除了肿瘤和坏死的肠,但该患者在术后因败血症过多和多器官衰竭而死亡。特别提及已建立的肠缺血对免疫功能的延迟作用,并建议这是本病例致命结果的主要因素。嗜铬细胞瘤患者的胃肠道症状的发作应提示可能发生肠缺血,并表明有必要迅速切除肿瘤。

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