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一名患有IIB型多发性内分泌腺瘤病和肾盂肾炎的患者发生嗜铬细胞瘤多系统危机。

Pheochromocytoma multisystem crisis in a patient with multiple endocrine neoplasia type IIB and pyelonephritis.

作者信息

Caputo Christopher, Fishbane Steven, Shapiro Lawrence, Courgi Robert G, Kostadinov Stefan, Donovan Virginia, Epstein David

机构信息

Division of Nephrology, and Department of Pathology, Winthrop-University Hospital, Mineola, NY, USA.

出版信息

Am J Kidney Dis. 2002 Jun;39(6):E23. doi: 10.1053/ajkd.2002.33414.

Abstract

A patient with pyelonephritis developed multiorgan failure resulting in death. Clinical findings were consistent with multiple endocrine neoplasia type II, with bilateral pheochromocytomas identified by computed tomography scan. We hypothesize that either the infection or the administration of radiocontrast media led to a massive release of catecholamines from the pheochromocytomas. As a result, tissue perfusion was severely compromised, and multiorgan failure developed. This exceedingly rare complication of pheochromocytoma has been termed pheochromocytoma multisystem crisis.

摘要

一名肾盂肾炎患者发展为多器官功能衰竭并导致死亡。临床发现与II型多发性内分泌肿瘤一致,计算机断层扫描确定双侧嗜铬细胞瘤。我们推测,感染或使用放射性造影剂导致嗜铬细胞瘤大量释放儿茶酚胺。结果,组织灌注严重受损,多器官功能衰竭发生。这种极其罕见的嗜铬细胞瘤并发症被称为嗜铬细胞瘤多系统危机。

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