已知高血压患者心悸,从表面上看:嗜铬细胞瘤合并甲状腺功能减退1例

A. Idowu, A. Mene, O. Salami, T. Ajiro, Daniel Ezuduemoih, C. Inyang
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引用次数: 0

摘要

嗜铬细胞瘤是一种罕见的肿瘤,起源于肾上腺髓质的嗜铬细胞。这是一种潜在的危及生命的内分泌紊乱。我们报告一个56岁的妇女谁提出了由于反复发作的心悸与额部头痛,并伴有视觉闪光和发作性出汗。腹部骨盆计算机断层扫描显示左肾上腺内边界清楚的均匀肿块。尿中肾上腺素和去甲肾上腺素明显升高,并对嗜铬细胞瘤进行评估。在排除心脏异常后,任何出现心悸和其他神经系统症状的患者都应强烈考虑嗜铬细胞瘤。在新诊断的高血压患者中,用超声筛查高血压的继发原因是很重要的,超声是便宜且容易获得的。同样,强烈建议对任何强烈怀疑嗜铬细胞瘤但血压正常的患者进行动态血压监测,以证明该模式的不稳定性。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Palpitation in a known hypertensive patient, looking beyond the obvious: A case of pheochromocytoma coexisting with hypothyroidism
Pheochromocytoma is an uncommon tumor arising from the chromaffin cells of the adrenal medulla. It is a potential life-threatening endocrine disorder. We report a case of a 56-year-old woman who presented on account of recurrent episodes of palpitation with frontal headache that was associated with visual flashes and episodic sweating. Abdominopelvic computed tomography scan showed a well-circumscribed homogeneous mass within the left adrenal gland. The urinary metanephrine and normetanephrine were markedly raised, with an assessment of pheochromocytoma made. Pheochromocytoma should be strongly considered in any patient presenting with palpitations and other neurological symptoms after ruling out cardiac abnormalities. It is important to screen for secondary cause of hypertension in a newly diagnosed hypertensive with ultrasound, which is cheap and readily available. Likewise, ambulatory blood pressure monitoring is highly recommended in any patient with strong suspicion of pheochromocytoma but with normal blood pressure to demonstrate the lability in the pattern.
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