Tzemos N, McNeill G P, Jung R T, MacDonald T M
Hypertension Research Centre, Department of Clinical Pharmacology & Therapeutics, Ninewells Hospital & Medical School, Dundee, DD I 9SY, United Kingdom.
Scott Med J. 2001 Feb;46(1):14-5. doi: 10.1177/003693300104600106.
Phaeochromocytomas are rare cause of secondary hypertension with significant morbidity and mortality, if left untreated. Paroxysms with hypertension are considered as "textbook" presentations but atypical forms represent considerable diagnostic challenge. We report an unusual association between phaeochromocyotoma and post-exertional malignant arrhythmia in a normotensive subject.
嗜铬细胞瘤是继发性高血压的罕见病因,若不治疗,会导致显著的发病率和死亡率。伴有高血压的发作被视为“教科书式”表现,但非典型形式具有相当大的诊断挑战性。我们报告了一名血压正常的患者中嗜铬细胞瘤与运动后恶性心律失常之间的不寻常关联。