Zhao Juping, Alimu Parehe, Dai Jun, Xie Jing, Xu Danfeng, Sun Fukang
Department of Urology, Shanghai JiaoTong University School of Medicine, Ruijin Hospital, Shanghai, China.
CRSLS. 2021 Feb 23;8(1). doi: 10.4293/CRSLS.2020.00079. eCollection 2021 Jan-Mar.
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.
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 Partial hormone replacement therapy was initiated postoperatively and withdrawn uneventfully 1 year after RLA in both patients, and both patients have recovered well.
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.
库欣综合征(CS)合并妊娠的情况罕见但风险高,给该疾病的临床诊断和治疗带来巨大挑战。
2016年8月至2019年8月,我们收治了两名因肾上腺肿瘤导致CS的孕妇。经过多学科会诊,她们因心力衰竭和严重低氧血症接受了急诊剖宫产,最终在辅助治疗后产下活婴。两名患者均在产后2.6个月和1.5个月接受了后腹腔镜肾上腺切除术(RLA),成功切除肾上腺肿瘤。术后病理证实肾上腺肿瘤为肾上腺皮质腺瘤。术后开始部分激素替代治疗,两名患者在RLA术后1年均顺利停药,且恢复良好。
妊娠早期很难发现CS,而在妊娠晚期发现时,由于需要兼顾母亲和胎儿的安全,往往风险极大,这需要多学科协调合作,积极调整剖宫产后的心肺功能和内环境,同时要知道及时进行RLA切除肾上腺皮质腺瘤可有效治愈CS。