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表现为部分性HELLP综合征的嗜铬细胞瘤

Pheochromocytoma Presenting as Partial HELLP Syndrome.

作者信息

Daaboul Yazan, Korjian Serge, Khalil Lamis, Nemr Rita

机构信息

Lebanese American University Medical Center-Rizk Hospital, Gilbert & Rose-Marie Chagoury School of Medicine, Lebanese American University, Byblos, Lebanon.

出版信息

Case Rep Obstet Gynecol. 2015;2015:294326. doi: 10.1155/2015/294326. Epub 2015 Aug 16.

Abstract

Diagnosis of pheochromocytoma in partial HELLP syndrome is extremely rare. We report a case of a 25-year-old multigravida woman at 30 weeks of gestation who presented with clinical features consistent with partial HELLP syndrome. Her symptoms were not controlled by pharmacologic therapy, and the patient underwent urgent cesarean section. The patient gave birth to a viable baby, but she sustained an episode of ventricular fibrillation intraoperatively that did not result in any long-term sequelae. The patient's symptoms persisted postoperatively and work-up for secondary etiologies of hypertension demonstrated a right adrenal pheochromocytoma. Following resection, the patient's signs and symptoms resolved, and her lab tests normalized.

摘要

部分性HELLP综合征合并嗜铬细胞瘤的诊断极为罕见。我们报告一例25岁多胎妊娠女性,孕30周,临床表现符合部分性HELLP综合征。其症状经药物治疗未能控制,患者接受了紧急剖宫产。患者产下一名存活婴儿,但术中发生了一次室颤,未留下任何长期后遗症。患者术后症状持续存在,对高血压的继发病因检查发现右侧肾上腺嗜铬细胞瘤。切除肿瘤后,患者的体征和症状消失,实验室检查结果恢复正常。

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