Atuk N O
Hosp Pract (Off Ed). 1983 Apr;18(4):187-202. doi: 10.1080/21548331.1983.11702524.
Pheochromocytoma is curable in 90% of cases, yet its diagnosis and localization are among the most challenging problems in clinical medicine. Although only 10% of these tumors are malignant, others may be lethal because of excessive circulating catecholamines. The clinical hallmark of pheochromocytoma is hypertension, but some patients are normotensive and may even be hypotensive.
嗜铬细胞瘤在90%的病例中是可治愈的,但其诊断和定位是临床医学中最具挑战性的问题之一。虽然这些肿瘤中只有10%是恶性的,但其他肿瘤可能因循环儿茶酚胺过多而致命。嗜铬细胞瘤的临床特征是高血压,但有些患者血压正常,甚至可能是低血压。