[分泌肾上腺素的嗜铬细胞瘤，一种罕见的表现形式]
[Pheochromocytoma secreting adrenaline, a rare form of presentation].
作者信息
Escobedo Palau J A, Chena Alejandro J A, Rubio Félix S A, Aznar Carbonell A, Sebastián Royo B, Fernández García A
机构信息
Servicio de Medicina Interna, Hospital General San Jorge, Huesca.
出版信息
An Med Interna. 1994 Feb;11(2):80-2.
PMID:8193239
Abstract
We present the case of a 42-year-old patient with a pheochromocytoma, whose clinical form of presentation was extremely rare, due to the high secretion of adrenalin compared to noradrenaline. We stress the relevance of the anamnesis for the diagnosis of this pathology, as well as the problems regarding its clinical, anaesthetic and surgical management. In addition, we review the literature.
摘要
我们报告一例42岁的嗜铬细胞瘤患者，其临床表现形式极为罕见，因为肾上腺素的分泌量高于去甲肾上腺素。我们强调病史对于该疾病诊断的相关性，以及其临床、麻醉和手术管理方面的问题。此外，我们还回顾了相关文献。
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An Med Interna. 1994 Feb;11(2):80-2.
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