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首页> 外文期刊>Journal of Pediatric Surgery Case Reports >Accessory hepatic lobes in the pediatric population: A report of three cases of torsion and literature review
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Accessory hepatic lobes in the pediatric population: A report of three cases of torsion and literature review

机译:小儿人群的肝旁叶:三例扭转病例报告并文献复习

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Congenital liver anomalies are uncommon. Symptomatic accessory hepatic lobes (AHL), either in continuity with the liver or ectopically located, are even less common. AHL have been reported in individuals spanning from neonates to octogenarians and are typically asymptomatic, however when symptomatic often require surgical intervention. We report three new cases of AHL in children (mean?=?14.6 years). All three presented with sudden onset of abdominal pain and were diagnosed preoperatively by imaging findings. All three patients had symptom resolution following resection of the torsed accessory liver lobes. We report here the largest series of pediatric AHL torsion at a single institution to date, review the classification schemes, identify diagnostic imaging findings, and summarize associated congenital disorders that should raise suspicion for accessory hepatic lobes.
机译:先天性肝异常并不常见。与肝脏连续或位于异位的有症状的肝副叶(AHL)更为罕见。据报道,从新生儿到八十岁的人,AHL均无症状,但是当有症状时通常需要手术干预。我们报告了三例新的儿童AHL病例(平均14.6岁)。这三人均表现为腹痛突然发作,并在术前通过影像学检查得到诊断。所有三名患者在切除扭转的副肝叶后均具有症状缓解。我们在这里报告了迄今为止单个机构中最大的儿科AHL扭转系列,回顾了分类方案,确定了诊断性影像学发现,并总结了相关的先天性疾病,这些疾病应引起对肝副叶的怀疑。

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