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继发于肾上腺腺瘤的继发性高血压患者成功妊娠:病例报告。

A successful pregnancy in a patient with secondary hypertension caused by adrenal adenoma: a case report.

机构信息

Department of cardiology, West China Hospital, Sichuan University, Chengdu, China.

Naidong People's Hospital, Shannan, Tibet Autonomous Region, China.

出版信息

BMC Pregnancy Childbirth. 2019 Apr 3;19(1):116. doi: 10.1186/s12884-019-2262-2.

Abstract

BACKGROUND

Secondary hypertension is a rare complication in pregnancy that causes poor outcomes, such as preeclampsia, premature delivery, intrauterine growth retardation, stillbirths, spontaneous abortion or intrauterine death. Cushing's disease caused by an adrenal adenoma is rare during pregnancy and may be overlooked by obstetricians and physicians, but can lead to hypertension, diabetes mellitus and an increased risk of fetal and maternal morbidity. Approximately 200 cases have been reported in the literature. Here, we report the successful management of a pregnant patient with Cushing's syndrome due to an adrenal adenoma.

CASE PRESENTATION

The 35-year-old Chinese female had no individual or family medical history of hypertension, and did not exhibit chronic kidney disease, diabetes mellitus, autoimmune and common endocrine diseases. Her blood pressure was elevated from the 16th week of gestation and was not controlled by 30 mg nifedipine twice a day. Examination in our department revealed her 24 h urinary free cortisol (24 h UFC) level was 1684.3 μg/24 h (normal range: 20.26-127.55 μg/24 h) and plasma adrenocorticotropic hormone was < 1.00 ng/L in three independent measurements (normal range: 5-78 ng/L). Ultrasonography demonstrated a mass (2.9 cm × 2.8 cm) in the right side of the adrenal gland. Magnetic resonance imaging without contrast showed a 3.2 cm diameter mass in the right-side of the adrenal gland. Other medical tests were normal. Laparoscopic adrenalectomy was performed at the 26th week of gestation by a urological surgeon in the West China Hospital. Histopathology revealed an adrenocortical adenoma. After surgery, the patient accepted glucocorticoid replacement therapy. The remaining trimester continued without complication and her blood pressure was normal at the 32nd week of gestation without antihypertensive therapy. The patient gave birth to a healthy boy at the 40th week of gestation.

CONCLUSIONS

Cushing's syndrome caused by adrenal adenoma is rare during pregnancy. This unique case suggested that analysis of the UFC level and circadian rhythm of plasma cortisol provides a suitable strategy to diagnose Cushing's syndrome during pregnancy. Laparoscopic surgical resection in the second trimester provides a reasonable approach to treat pregnant patients exhibiting Cushing's syndrome caused by an adrenal adenoma.

摘要

背景

继发性高血压是妊娠的一种罕见并发症,可导致不良后果,如子痫前期、早产、宫内生长迟缓、死胎、自然流产或宫内死亡。妊娠期间由肾上腺腺瘤引起的库欣病很少见,可能被产科医生和内科医生忽视,但可导致高血压、糖尿病和胎儿及产妇发病率增加。文献中约有 200 例报道。在此,我们报告了一例成功治疗妊娠合并肾上腺腺瘤所致库欣综合征的病例。

病例介绍

这名 35 岁的中国女性无个体或家族高血压病史,也无慢性肾脏病、糖尿病、自身免疫性和常见内分泌疾病病史。她从妊娠第 16 周开始血压升高,每天两次服用硝苯地平 30mg 也无法控制。我院检查发现,她的 24 小时尿游离皮质醇(24h UFC)水平为 1684.3μg/24h(正常范围:20.26-127.55μg/24h),3 次独立测量的血浆促肾上腺皮质激素均<1.00ng/L(正常范围:5-78ng/L)。超声检查显示肾上腺右侧有一肿块(2.9cm×2.8cm)。磁共振成像(无对比剂)显示肾上腺右侧有一个 3.2cm 直径的肿块。其他医学检查均正常。由华西医院的泌尿外科医生在妊娠 26 周时进行了腹腔镜肾上腺切除术。组织病理学显示为肾上腺皮质腺瘤。手术后,患者接受了糖皮质激素替代治疗。剩余的孕程继续进行,没有并发症,在妊娠 32 周时血压正常,无需降压治疗。患者在妊娠第 40 周时产下一名健康男婴。

结论

妊娠期间由肾上腺腺瘤引起的库欣综合征很少见。这个独特的病例表明,分析 UFC 水平和皮质醇的昼夜节律为妊娠期间库欣综合征的诊断提供了一种合适的策略。妊娠中期的腹腔镜手术切除为治疗妊娠合并肾上腺腺瘤所致库欣综合征的孕妇提供了一种合理的方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d59b/6448298/18f33d9b37fb/12884_2019_2262_Fig1_HTML.jpg

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