Chawanpaiboon Saifon, Janchua Mahapop, Luamprapat Pimkul, Chawanpaiboon Piramon, Maimaen Suphisara
Division of Maternal-Fetal Medicine, Department of Obstetrics and Gynecology, Faculty of Medicine Siriraj Hospital, Mahidol University, Bangkok, Thailand.
Am J Case Rep. 2025 Apr 13;26:e946909. doi: 10.12659/AJCR.946909.
BACKGROUND Spontaneous liver rupture during pregnancy is a rare but life-threatening condition with high maternal and perinatal mortality. It is commonly associated with HELLP (hemolysis, elevated liver enzymes, and low platelet count) syndrome, preeclampsia, and liver-related diseases, making diagnosis and management challenging due to non-specific symptoms. Immediate intervention and a multidisciplinary approach are crucial for improving outcomes. CASE REPORT A 34-year-old primigravida woman at 35+5 weeks of gestation presented with severe epigastric pain, nausea, and vomiting. Initially treated for GERD, her symptoms persisted. Ultrasound revealed a fetus appropriate for gestational age (AGA) with normal well-being, amniotic fluid levels, and intact placental attachment. However, intra-abdominal visualization was limited due to advanced gestation and suspected bleeding around the uterus. As the patient's condition deteriorated, emergency surgery was performed, revealing a large liver mass rupture with significant intra-abdominal bleeding. Perihepatic packing was used for stabilization. Subsequent imaging identified a subcapsular hematoma in hepatic segments 2/3. A second surgery was performed, and a lateral segmentectomy was completed. Both the mother and baby recovered well, with the Jackson-Pratt drain removed on postoperative day 3 and discharge on day 7. CONCLUSIONS Spontaneous liver rupture, although rare, should be considered in pregnant patients with unexplained abdominal pain, even in the absence of typical risk factors. Early surgical intervention, timely imaging, and a multidisciplinary approach are critical for successful outcomes. Perihepatic packing serves as a lifesaving temporary measure to control bleeding and allow for further surgical planning.
妊娠期自发性肝破裂是一种罕见但危及生命的疾病,孕产妇和围产儿死亡率很高。它通常与HELLP(溶血、肝酶升高和血小板计数降低)综合征、先兆子痫及肝脏相关疾病有关,由于症状不具特异性,使得诊断和管理具有挑战性。立即干预和多学科方法对于改善预后至关重要。病例报告:一名34岁初产妇,孕35+5周,出现严重上腹痛、恶心和呕吐。最初按胃食管反流病治疗,但其症状持续存在。超声检查显示胎儿与孕周相符(AGA),状况良好,羊水水平正常,胎盘附着完整。然而,由于孕周较大且怀疑子宫周围出血,腹腔内可视化受限。随着患者病情恶化,进行了急诊手术,发现一个大的肝脏肿物破裂,腹腔内有大量出血。采用肝周填塞进行止血。随后的影像学检查发现肝2/3段有包膜下血肿。进行了第二次手术,完成了左外叶切除术。母婴恢复良好,术后第3天拔除杰克逊-普拉特引流管,第7天出院。结论:自发性肝破裂虽然罕见,但对于有不明原因腹痛的孕妇,即使没有典型危险因素,也应予以考虑。早期手术干预、及时的影像学检查和多学科方法对于取得成功的治疗结果至关重要。肝周填塞是一种挽救生命的临时措施,可控制出血并为进一步的手术规划创造条件。