Langerman Alexander, Schneider John A, Ward R Parker
Section of Cardiology, Department of Medicine, University of Chicago, Chicago, Illinois, USA.
Rev Cardiovasc Med. 2004 Fall;5(4):226-30.
Pheochromocytomas are neuroendocrine tumors that typically present with paroxysms of hypertension, but occasionally can lead to marked hemodynamic instability, left ventricular dysfunction, and cardiovascular collapse. Although pheochromocytoma in pregnancy is rare, factors specific to pregnancy can precipitate catecholamine crisis, making diagnosis and treatment challenging. We present a case of acute cardiovascular collapse with transient left ventricular dysfunction due to catecholamine crisis in a healthy young woman at term pregnancy. Further clinical and genetic investigation revealed pheochromocytoma as part of multiple endocrine neoplasia IIa (Sipple syndrome). A discussion of diagnosis and treatment strategies for pheochromocytoma in pregnancy and acute catecholamine crisis accompanies this report.
嗜铬细胞瘤是一种神经内分泌肿瘤,通常表现为阵发性高血压,但偶尔也会导致明显的血流动力学不稳定、左心室功能障碍和心血管衰竭。虽然妊娠合并嗜铬细胞瘤很少见,但妊娠特有的因素可引发儿茶酚胺危机,使诊断和治疗具有挑战性。我们报告一例足月妊娠的健康年轻女性因儿茶酚胺危机导致急性心血管衰竭并伴有短暂性左心室功能障碍的病例。进一步的临床和基因调查显示嗜铬细胞瘤是多发性内分泌腺瘤病IIa型(西普尔综合征)的一部分。本报告还讨论了妊娠合并嗜铬细胞瘤及急性儿茶酚胺危机的诊断和治疗策略。