Elradi Wiaam, Innayat Samreen, Hanafy Ahmed, Naseem Sharifah, Awadelkareem Abuzar, Meneni Deepika
Obstetrics and Gynaecology Department, The James Cook University Hospital, South Tees NHS Foundation Trust, Middlesbrough, United Kingdom.
Obstetrics and Gynaecology Department, The James Cook University Hospital, South Tees NHS Foundation Trust, Middlesbrough, United Kingdom.
Clin Med (Lond). 2025 Mar;25(2):100288. doi: 10.1016/j.clinme.2025.100288. Epub 2025 Jan 24.
Adrenal haemorrhage in pregnancy is rare but can lead to significant maternal and fetal morbidity if unrecognised. We present the case of a 25-year-old woman in her second pregnancy, who was admitted at 34 + 4 weeks of gestation with severe abdominal pain. Despite initial unremarkable assessments, further imaging revealed a left adrenal haemorrhage, with evidence of prior right adrenal infarction, resulting in primary adrenal insufficiency. Haematological investigations later confirmed heterozygous factor V Leiden as a likely contributing factor. This report underscores the diagnostic challenges of adrenal pathology in pregnancy, where symptoms may overlap with more common conditions. Immediate management with hydrocortisone therapy, supported by a multidisciplinary team (MDT), was employed, with a successful outcome for both mother and child following delivery by caesarean section.
妊娠期肾上腺出血罕见,但如果未被识别,可导致严重的母婴发病。我们报告一例25岁的二胎孕妇,在妊娠34 + 4周时因严重腹痛入院。尽管初始评估无异常,但进一步影像学检查发现左侧肾上腺出血,并有既往右侧肾上腺梗死的证据,导致原发性肾上腺功能不全。血液学检查后来证实杂合子因子V莱顿突变可能是一个促成因素。本报告强调了妊娠期肾上腺病变的诊断挑战,其症状可能与更常见的情况重叠。在多学科团队(MDT)的支持下,立即采用氢化可的松治疗,剖宫产分娩后母婴均获得成功结局。