医学
脾切除术
脾静脉
怀孕
外科
腹痛
妊娠期
胎儿
脾脏
静脉
放射科
门脉高压
内科学
肝硬化
生物
遗传学
作者
Daniel Kane,John F. Keaney,Elizabeth Tunney,Ronan Daly,Emma Doyle,John B. Conneely,Conán McCaul,Michael Geary,Jennifer Donnelly,Claire McCarthy
摘要
Abstract 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.
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