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嗜铬细胞瘤

Phaeochromocytoma.

作者信息

Foo M, Burton B J, Ahmed R

机构信息

Department of Nephrology, Middlesex Hospital, London.

出版信息

Br J Hosp Med. 1995;54(7):318-21.

PMID:8556210
Abstract

Phaeochromocytomas are rare catecholamine-secreting tumours which can mimic a variety of common clinical conditions, such as hypertension and angina. It is a potentially curable condition if discovered early, and clinicians should be alerted as to its presence in a young individual with hypertension or atypical angina-associated hypertension. Pharmacological mismanagement can cause fatal hypertensive crisis.

摘要

嗜铬细胞瘤是一种罕见的分泌儿茶酚胺的肿瘤,可模拟多种常见临床病症,如高血压和心绞痛。如果早期发现,这是一种潜在可治愈的病症,临床医生应警惕其在患有高血压或非典型心绞痛相关性高血压的年轻个体中的存在。药物治疗管理不当可导致致命的高血压危象。

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