Kane Daniel, Keaney John M, Tunney Elizabeth, Daly Ronan, Doyle Emma, Conneely John B, McCaul Conan, Geary Michael, Donnelly Jennifer, McCarthy Claire M
Department of Obstetrics & Gynaecology, Royal College of Surgeons in Ireland, Rotunda Hospital, Dublin 1, Ireland.
School of Medicine, Royal College of Surgeons in Ireland, St Stephens Green, Dublin 2, Ireland.
Int J Gynaecol Obstet. 2025 Jan;168(1):63-68. doi: 10.1002/ijgo.15842. Epub 2024 Aug 1.
Splenic vein aneurysm (SVA) rupture is a rare clinical entity, with few case reports detailing its occurrence during pregnancy. We describe a case of a SVA rupture and present a systematic review of the literature in relation to splenic vein rupture, with or without aneurysm. Our case was of a 30-year-old woman, Para 4 at 37 weeks' gestation who presented with significant abdominal pain and subsequent maternal collapse. Massive intra-abdominal hemorrhage was identified, with splenic vessel rupture suspected. A splenectomy and partial pancreatectomy were performed along with massive blood product transfusion. There was both maternal and fetal survival with no long-term sequelae at follow-up. Histological examination of the spleen and its vessels noted a SVA rupture. In a subsequent systematic review of the literature, we identified 10 cases of splenic vein rupture with only two previously documented cases of SVA rupture in pregnancy. Maternal and fetal survival has only been reported in two cases of splenic vein rupture, with ours being a third.
脾静脉动脉瘤(SVA)破裂是一种罕见的临床情况,仅有少数病例报告详细描述了其在妊娠期的发生情况。我们报告一例SVA破裂病例,并对有或无动脉瘤的脾静脉破裂相关文献进行系统综述。我们的病例是一名30岁、孕4产的女性,孕37周时出现严重腹痛,随后母体发生虚脱。经诊断为腹腔内大量出血,怀疑脾血管破裂。遂行脾切除术和部分胰腺切除术,并大量输注血制品。母体和胎儿均存活,随访无长期后遗症。脾脏及其血管的组织学检查发现SVA破裂。在随后对文献的系统综述中,我们确定了10例脾静脉破裂病例,其中仅有2例先前记录的妊娠期SVA破裂病例。仅有2例脾静脉破裂病例报告了母体和胎儿存活情况,我们的病例是第三例。