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腹腔镜治疗嗜铬细胞瘤后的成功妊娠结局

Successful Pregnancy Outcomes After Laparoscopic Management of Pheochromocytoma.

作者信息

Prakash Pradeep, Kulshrestha Vidushi, Ramachandran Rashmi, Kumar Rajeev

机构信息

Department of Urology, All India Institute of Medical Sciences, New Delhi, India.

Department of Obstetrics and Gynaecology, All India Institute of Medical Sciences, New Delhi, India.

出版信息

J Endourol Case Rep. 2020 Sep 17;6(3):170-173. doi: 10.1089/cren.2019.0139. eCollection 2020.

Abstract

Pheochromocytoma is a rare cause of hypertension in pregnancy, which is often overlooked; especially in late pregnancy because of more prevalent pre-eclampsia. It has been associated with significant morbidity and mortality rates in both mother and fetus, if not diagnosed and treated in time. Minimally invasive surgery has been infrequently used for surgical management of pheochromocytoma in pregnancy, with <20 reported cases in English literature. A 26-year-old pregnant woman presented at 9 weeks of gestation with complaints of palpitations, sweating, and headache; with past history of first trimester spontaneous abortion caused by accelerated hypertension. She was found to have hypertension and diabetes, but no pedal edema, weight gain, or proteinuria. Ultrasonogram and MRI of abdomen revealed a left adrenal mass and 24 hours urinary catecholamines levels were increased, suggesting a pheochromocytoma. After preoperative optimization in consultations with obstetricians, endocrinologists, and anesthetists, she underwent laparoscopic left adrenalectomy during 15th week of gestation. Perioperative hospital course was uneventful for both mother and the fetus. After adrenalectomy, her diabetes was cured and hypertension was controlled with single antihypertensive. She was readmitted at 31 weeks of gestation with accelerated hypertension and underwent emergency caesarean for impending eclampsia at 32 weeks, and delivered a healthy female baby. 131I-meta-iodobenzylguanidine (MIBG) scan and 68Ga-[1,4,7,10-tetraazacyclododecane-1,4,7,10-tetraacetic acid]-1-NaI(3)-octreotide positron emission tomography-CT (68Ga-DOTANOC PET-CT) scan was obtained in postpartum period to rule out any extra-adrenal pheochromocytoma, both of which did not reveal any abnormality. At 1 year follow-up, she is normoglycemic and hypertension controlled on single antihypertensive. Pheochromocytoma in pregnancy is a rare but potentially lethal condition, and high index of suspicion is required for early diagnosis. Multidisciplinary coordination is required for effective management of this rare condition. Laparoscopic adrenalectomy is safe in second trimester of pregnancy for both mother and fetus.

摘要

嗜铬细胞瘤是妊娠期高血压的罕见病因,常被忽视;尤其是在妊娠晚期,因为子痫前期更为常见。如果不及时诊断和治疗,它与母亲和胎儿的高发病率和死亡率相关。微创手术很少用于妊娠期嗜铬细胞瘤的手术治疗,英文文献报道的病例不到20例。一名26岁孕妇在妊娠9周时出现心悸、出汗和头痛;既往有孕早期因高血压加速导致自然流产史。她被发现患有高血压和糖尿病,但无足背水肿、体重增加或蛋白尿。腹部超声和MRI显示左肾上腺肿块,24小时尿儿茶酚胺水平升高,提示嗜铬细胞瘤。在与产科医生、内分泌学家和麻醉师会诊进行术前优化后,她在妊娠第15周接受了腹腔镜左肾上腺切除术。围手术期母亲和胎儿的住院过程均顺利。肾上腺切除术后,她的糖尿病治愈,高血压用单一降压药控制。她在妊娠31周时因高血压加速再次入院,并在32周时因即将发生子痫接受急诊剖宫产,产下一名健康女婴。产后进行了131I-间碘苄胍(MIBG)扫描和68Ga-[1,4,7,10-四氮杂环十二烷-1,4,7,10-四乙酸]-1-NaI(3)-奥曲肽正电子发射断层扫描-CT(68Ga-DOTANOC PET-CT)扫描,以排除任何肾上腺外嗜铬细胞瘤,两者均未显示任何异常。在1年的随访中,她血糖正常,高血压用单一降压药控制。妊娠期嗜铬细胞瘤是一种罕见但可能致命的疾病,早期诊断需要高度的怀疑指数。有效管理这种罕见疾病需要多学科协调。妊娠中期腹腔镜肾上腺切除术对母亲和胎儿都是安全的。

相似文献

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Successful Pregnancy Outcomes After Laparoscopic Management of Pheochromocytoma.腹腔镜治疗嗜铬细胞瘤后的成功妊娠结局
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本文引用的文献

2
Pheochromocytoma and pregnancy: a deceptive connection.嗜铬细胞瘤与妊娠:一种具有欺骗性的关联。
Eur J Endocrinol. 2012 Feb;166(2):143-50. doi: 10.1530/EJE-11-0528. Epub 2011 Sep 2.
3
Minimally invasive adrenalectomy for pheochromocytoma during pregnancy.妊娠期嗜铬细胞瘤的微创肾上腺切除术
Surg Laparosc Endosc Percutan Tech. 2002 Apr;12(2):122-5. doi: 10.1097/00129689-200204000-00011.
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Pheochromocytoma associated with pregnancy: case report and review of the literature.
Obstet Gynecol Surv. 1999 Nov;54(11):728-37. doi: 10.1097/00006254-199911000-00025.

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