Hypertension secondary to pheochromocytoma.
Hypertension secondary to pheochromocytoma.
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继发于嗜铬细胞瘤的高血压。
DOI：
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发表时间：
1982
期刊：
影响因子：
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通讯作者：
R. Gifford
中科院分区：
文献类型：
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作者：
W. Manger;R. Gifford
嗜铬细胞瘤的临床表现往往是戏剧性的和爆炸性的，并且是如此的多变，以至于它理所当然地赢得了“大模仿者”的称号。从组织学上不能确定嗜铬细胞瘤是良性还是恶性。虽然只有10%的肿瘤在病理上是恶性的，如转移或浸润邻近组织，但如果不适当治疗，过量循环儿茶酚胺（肾上腺素和去甲肾上腺素）的作用几乎总是导致致命的并发症。所有有轻微嗜铬细胞瘤表现的患者都必须进行筛查。
The clinical expressions of pheochromocytoma are often dramatic and explosive, and are so variable that it has rightly earned the title of the ‘great mimic’ [1]. One cannot determine histologically whether a pheochromocytoma is benign or malignant. Although only 10% of these neoplasms are pathologically malignant, as evidenced by metastasis or invasion of adjacent tissue, lethal complications from the effects of excessive circulating catecholamines (epinephrine and norepinephrine) almost invariably result if the disease is not appropriately treated. All patients with manifestations even remotely suggestive of pheochromocytoma must be screened for this disease.