Splenic artery aneurysm rupture in a pregnant woman with hepatosplenic schistosomiasis: case report and literature review

IF 0.8 Q4 GASTROENTEROLOGY & HEPATOLOGY Egyptian Liver Journal Pub Date : 2024-01-29 DOI:10.1186/s43066-024-00314-x
Chantelli Iamblaudiot Razafindrazoto, Antsa Fihobiana Randrianiaina, Behoavy Mahafaly Ralaizanaka, Henintsoa Rakotoniaina, Nitah Harivony Randriamifidy, Anjaramalala Sitraka Rasolonjatovo, Andry Lalaina Rinà Rakotozafindrabe, Tovo Harimanana Rabenjanahary, Soloniaina Hélio Razafimahefa, Rado Manitrala Ramanampamonjy
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Abstract

Pregnancy is not uncommon in patients with non-cirrhotic portal hypertension. Rupture of a splenic artery aneurysm remains a rare complication, associated with a very poor maternal–fetal prognosis. Our aim is to report a case of ruptured splenic aneurysm and to show the maternal–fetal over-risks during the association of pregnancy and portal hypertension, even in non-cirrhotic patients. We report a case of a 34-year-old woman, pregnant at 24 weeks gestation, with non-cirrhotic portal hypertension due to hepatic schistosomiasis. She was hospitalized for variceal bleeding. Patient had undergone endoscopic variceal band ligation and no bleeding recurrence. An unexplained hypovolemic shock appeared during the hospitalization with the occurrence of an in utero fetal death. The fetus was delivered by vaginal delivery. Abdominal CT scan angiogram showed a splenic artery aneurysm rupture. The patient underwent an emergency laparotomy with ligation of the splenic artery associated with splenectomy. Postoperative course was simple. Management of portal hypertension was continued at discharge (diuretic, beta-blockers, and esophageal varices ligation). The association of pregnancy and portal hypertension remains a serious situation with a high risk of maternal–fetal complications. Splenic artery aneurysm rupture is one of the rare complications of this association with a very poor maternal–fetal prognosis. Open repair is the surgical treatment of choice with a non-negligible morbi-mortality.
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一名患有肝脾血吸虫病的孕妇脾动脉瘤破裂:病例报告和文献综述
非肝硬化性门静脉高压症患者怀孕并不少见。脾动脉瘤破裂仍然是一种罕见的并发症,母婴预后极差。我们的目的是报告一例脾动脉瘤破裂的病例,并说明妊娠与门静脉高压症(即使是非肝硬化患者)相关的母胎风险。我们报告了一例 34 岁妇女的病例,她在妊娠 24 周时怀孕,因肝血吸虫病而患有非肝硬化性门脉高压症。她因静脉曲张出血住院治疗。患者接受了内镜下静脉曲张带结扎术,没有再出血。住院期间出现不明原因的低血容量性休克,并导致宫内胎儿死亡。胎儿经阴道分娩。腹部 CT 血管造影显示脾动脉瘤破裂。患者接受了紧急开腹手术,结扎了脾动脉并进行了脾切除术。术后过程很简单。出院时继续接受门脉高压治疗(利尿剂、β-受体阻滞剂和食道静脉曲张结扎术)。妊娠合并门静脉高压症的情况仍然很严重,母婴并发症的风险很高。脾动脉瘤破裂是这种并发症的罕见并发症之一,母胎预后极差。开腹修补术是首选的外科治疗方法,其死亡率不可忽略。
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来源期刊
Egyptian Liver Journal
Egyptian Liver Journal Medicine-Hepatology
CiteScore
1.60
自引率
0.00%
发文量
60
审稿时长
9 weeks
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