肾上腺肿瘤致高危孕妇库欣综合征的诊断与治疗。

CRSLS : MIS case reports from SLS Pub Date : 2021-02-23 eCollection Date: 2021-01-01 DOI:10.4293/CRSLS.2020.00079
Juping Zhao, Parehe Alimu, Jun Dai, Jing Xie, Danfeng Xu, Fukang Sun
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引用次数: 0

摘要

妊娠合并库欣综合征(Cushing syndrome, CS)发生率低但危险性高,给临床诊断和治疗带来很大挑战。病例描述:2016年8月至2019年8月收治2例肾上腺肿瘤所致CS孕妇。经多学科会诊,因心力衰竭及严重低氧血症,行紧急剖宫产,经辅助治疗后最终产下活婴。术后2.6个月和1.5个月分别行后腹腔镜肾上腺切除术(RLA),成功切除肾上腺肿瘤。术后病理证实为肾上腺皮质腺瘤。两例患者术后开始部分激素替代治疗,并在RLA后1年顺利退出,两例患者均恢复良好。结论:妊娠早期难以发现CS,妊娠晚期发现CS时,因需兼顾母胎安全,往往存在较大风险,需要多学科协调配合,积极调整剖宫产术后心肺功能和内环境,及时行RLA切除肾上腺皮质腺瘤可有效治愈CS。
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Diagnosis and Treatment of High-risk Pregnant Women With Cushing Syndrome Caused by Adrenal Tumor.

Introduction: The occurrence of pregnancy with Cushing syndrome (CS) is rare but with high risks, posing a great challenge to the clinical diagnosis and treatment of the disease.

Case description: From Aug 2016 to Aug 2019, we admitted two pregnant women with CS caused by adrenal tumors. After multidisciplinary consultation, they underwent emergency Cesarean section because of heart failure and severe hypoxemia, and finally delivered a living baby after adjuvant therapy. Both patients underwent retroperitoneal laparoscopic adrenectomy (RLA) 2.6 and 1.5 months postpartum to have the adrenal tumors removed successfully. The postoperative pathology confirmed the adrenal tumor as adrenocortical adenoma. Partial hormone replacement therapy was initiated postoperatively and withdrawn uneventfully 1 year after RLA in both patients, and both patients have recovered well.

Conclusions: It is difficult to find CS in early pregnancy, and when it is detected in late pregnancy, it often poses a great risk because it is necessary to consider the safety of both mother and fetus, which requires multidisciplinary coordination and cooperation to positively adjust the cardiopulmonary function and internal environment after Cesarean section, knowing that timely RLA to remove the adrenocortical adenoma can effectively cure CS.

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