Sukor Norlela, Saidin Rashidi, Kamaruddin Nor Azmi
Department of Medicine, Hospital Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
South Med J. 2007 Jan;100(1):73-4. doi: 10.1097/01.smj.0000253008.77358.f3.
Pheochromocytomas are rare neuroendocrine tumors that produce, metabolize, and usually secrete catecholamines. Although hypertension is a common presenting feature of pheochromocytoma, the tumors occur (or are present) in only 0.1% of patients with hypertension. The variability of symptoms and rarity of occurrence render these tumors difficult to diagnose; many are discovered incidentally during radiological examination or at autopsy. A patient is presented with a pheochromocytoma that was discovered incidentally when she presented with abdominal pain and a normal blood pressure.
嗜铬细胞瘤是一种罕见的神经内分泌肿瘤,可产生、代谢并通常分泌儿茶酚胺。虽然高血压是嗜铬细胞瘤常见的临床表现,但该肿瘤仅见于0.1%的高血压患者。症状的多样性和发病率低使得这些肿瘤难以诊断;许多是在放射学检查或尸检时偶然发现的。本文报告一例嗜铬细胞瘤患者,该患者因腹痛就诊,血压正常,偶然发现患有嗜铬细胞瘤。