Chen Han, Xu Yiyao, Lu Xin, Jin Bao
Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No.1, Shuaifuyuan, Beijing, 100730, China; Department of General Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No.1, Shuaifuyuan, Beijing, 100730, China.
Department of Liver Surgery, Peking Union Medical College Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, No.1, Shuaifuyuan, Beijing, 100730, China.
Int J Surg Case Rep. 2025 Oct;135:111900. doi: 10.1016/j.ijscr.2025.111900. Epub 2025 Sep 4.
Giant splenic hemangiomas are rare and pose diagnostic and management challenges, particularly during pregnancy. This case highlights the need for multidisciplinary approach to manage such a massive splenic lesion in the second trimester.
A 34-year-old woman with pre-pregnancy splenic cysts developed left upper quadrant distension at 19 weeks of gestation. Physical examination and preoperative ultrasound confirmed splenic enlargement. Due to concerns for splenic rupture from uterine compression, open splenectomy was performed at 19 weeks + 5 days. Histopathology analysis confirmed splenic hemangioma.
Management of splenic hemangioma or other types of massive splenic mass lacks standardized guideline. And imaging alone cannot reliably differentiate type of splenic lesions. In pregnant patients, management should be individualized based on lesion size, symptoms, gestational age, and complication risk of conservative approaches. Treatment options necessitate multidisciplinary collaboration to balance maternal-fetal safety.
This case of giant splenic hemangioma during pregnancy demonstrates that splenectomy in the second trimester is feasible after balancing balance maternal-fetal risks. It emphasizes the necessity of multidisciplinary decision-making to optimize maternal and fetal outcomes in management of complex abdominal masses during pregnancy.
巨大脾脏血管瘤罕见,对诊断和治疗构成挑战,尤其是在孕期。本病例强调了在孕中期处理如此巨大的脾脏病变时采用多学科方法的必要性。
一名孕前患有脾脏囊肿的34岁女性,在妊娠19周时出现左上腹膨隆。体格检查和术前超声检查证实脾脏肿大。由于担心子宫压迫导致脾脏破裂,于妊娠19周+5天行开放性脾切除术。组织病理学分析证实为脾脏血管瘤。
脾脏血管瘤或其他类型的巨大脾脏肿物的治疗缺乏标准化指南。仅靠影像学检查无法可靠地区分脾脏病变的类型。对于孕妇,应根据病变大小、症状、孕周以及保守治疗方法的并发症风险进行个体化管理。治疗方案需要多学科协作以平衡母婴安全。
该例孕期巨大脾脏血管瘤表明,在权衡母婴风险后,孕中期行脾切除术是可行的。它强调了在孕期复杂腹部肿物管理中进行多学科决策以优化母婴结局的必要性。