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首页> 外文期刊>Journal of Pediatric Surgery Case Reports >Laparoscopic resection of a torsed accessory hepatic lobe: Case report and literature review
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Laparoscopic resection of a torsed accessory hepatic lobe: Case report and literature review

机译:腹腔镜切除扭转性副肝叶:病例报告和文献复习

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Accessory hepatic lobe (AHL) is a rare anatomical variant of the liver that is often asymptomatic and discovered incidentally through radiographic imaging. When pedunculated, AHL can undergo ischemic torsion, presenting as severe abdominal pain. Laparoscopic surgery provides an excellent approach to establish the definitive diagnose and excise the offending lobe. In our case, a 12-year-old boy presented with severe abdominal pain. Abdominal ultrasound and computer tomography demonstrated a mass adjacent to the liver with surrounding inflammation. The patient underwent diagnostic laparoscopy and a pedunculated AHL was discovered that had undergone 360° torsion. The ischemic-appearing lobe was resected laparoscopically without complications. Pathology confirmed hemorrhagic necrosis of otherwise normal hepatic tissue. The patient was discharged on the second postoperative day after an uneventful recovery. Due to the rarity of AHL, the definitive diagnosis of AHL torsion is typically made during exploratory laparotomy. A laparoscopic approach provides a safe and effective way to explore, diagnose and excise an ischemic AHL.
机译:辅助肝叶(AHL)是一种罕见的肝脏解剖变异,通常无症状,并通过X线影像学偶然发现。当带蒂时,AHL会发生缺血性扭转,表现为严重的腹痛。腹腔镜手术提供了一种极好的方法来进行明确的诊断并切除病灶。在我们的案例中,一个12岁男孩表现出严重的腹痛。腹部超声和计算机断层扫描显示邻近肝脏的肿块伴有周围炎症。该患者接受了诊断性腹腔镜检查,发现带蒂的AHL经受了360°扭转。腹腔镜下切除出现缺血的肺叶,无并发症。病理证实原为正常肝组织的出血坏死。患者恢复良好后,在术后第二天出院。由于AHL的罕见性,AHL扭转的确定性诊断通常在探索性剖腹手术中进行。腹腔镜方法为探索,诊断和切除缺血性AHL提供了一种安全有效的方法。

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