[Pheochromocytoma: diagnosis and treatment].

R Rosenthal, D Conen
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Abstract

Phaeochromocytoma is a rare tumour which produces a variety of symptoms. The most important factor is to think of the diagnosis, and there are many biochemical and pharmacological tests as well as radiological procedures to confirm it. Once the phaeochromocytoma is localised, it should, if possible, be removed. Surgery is the treatment of choice. In 1972 Ross described the diagnosis and therapy as "think of it, confirm it, find it and remove it". Today, 28 years later, this paper reviews the diagnosis and therapy of phaeochromocytoma under these key headings.

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嗜铬细胞瘤的诊断与治疗。
嗜铬细胞瘤是一种罕见的肿瘤,具有多种症状。最重要的因素是考虑诊断,有许多生化和药理学测试以及放射程序来证实它。一旦嗜铬细胞瘤被定位,如果可能的话,应将其切除。手术是治疗的首选。1972年,罗斯将诊断和治疗描述为“思考、确认、发现并去除它”。28年后的今天,本文在这些关键标题下回顾了嗜铬细胞瘤的诊断和治疗。
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