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嗜铬细胞瘤和肾动脉狭窄均为罕见疾患。显然,二者共存的情况则是极为少见,自1958年Harrison氏等首次报告以来,至今已有25例报道。发生此二元性高血压疾患的机制有三种主要类型:一为来自肾上腺或植物神经节的
Pheochromocytoma and renal artery stenosis are rare disorders. Obviously, the coexistence between the two is extremely rare. Since the first report of Harrison et al in 1958, there have been 25 reports so far. There are three main types of mechanisms of this dual hypertension disorder: one is from the adrenal gland or autonomic ganglion