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表现为休克的嗜铬细胞瘤。

Pheochromocytoma presenting as shock.

作者信息

Bergland B E

机构信息

Emergency Department, Estes Park Medical Center, CO 80517.

出版信息

Am J Emerg Med. 1989 Jan;7(1):44-8. doi: 10.1016/0735-6757(89)90084-3.

Abstract

539 cases of pheochromocytoma were reviewed with specific attention to those cases presenting with shock at initial evaluation. Eleven such cases were discovered, for an incidence of 2%. A 12th such case is reported here. The literature is discussed with consideration for diagnosis and management of the patient in unexplained shock, suggesting that such patients may be experiencing cardiovascular collapse secondary to massive catecholamine release from a previously undiagnosed pheochromocytoma. Therapeutic considerations are also discussed.

摘要

回顾了539例嗜铬细胞瘤病例,特别关注初诊时出现休克的病例。发现了11例此类病例,发病率为2%。本文报告第12例此类病例。讨论了相关文献,考虑了不明原因休克患者的诊断和管理,提示此类患者可能正经历因先前未诊断出的嗜铬细胞瘤大量释放儿茶酚胺继发的心血管衰竭。还讨论了治疗方面的考虑因素。

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