儿童大间充质肝错构瘤1例报告。

IF 0.6 Q4 SURGERY
Case Reports in Surgery Pub Date : 2025-04-30 eCollection Date: 2025-01-01 DOI:10.1155/cris/1929050
Alhasan H Alhebshi, Ammar Kabbarah, Murad Aljiffry
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引用次数: 0

摘要

良性肝肿瘤在儿童年龄组中很少观察到,据报道发病率为每年百万分之0.7。其中间充质错构瘤占18%-29%。影像学检查通常显示边缘良好的孤立肿块,通常可达30厘米。肿块主要位于右肝叶(75%的病例),可表现为带梗结构。我们报告一个1岁零9个月大的男孩被诊断为肝间充质错构瘤。腹部增强计算机断层扫描和磁共振成像(MRI)显示一个大的多室分隔肝病变,大小约为13.6 × 17.7 cm,显示多个部分增厚的内分隔。该手术以扩展右肝切除4A段和胆囊切除术的形式完成。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Large Mesenchymal Hepatic Hamartoma in Pediatric Age: A Case Report.

Benign liver tumors are infrequently observed in the pediatric age group, with an incidence reported at 0.7 per million population annually. Among these tumors, mesenchymal hamartoma constitutes 18%-29%. Imaging studies commonly reveal a well-marginated, solitary mass, often measuring up to 30 cm. The mass, primarily located in the right liver lobe (75% of cases), may exhibit a pedunculated structure. We present a case of a 1-year-and-9-month-old boy diagnosed with hepatic mesenchymal hamartoma. A contrast-enhanced computed tomography of the abdomen and magnetic resonance imaging (MRI) were performed and demonstrated a large multiloculated septated liver lesion measuring approximately 13.6 × 17.7 cm, demonstrating multiple partially thickened internal septations. The procedure was done for the patient in the form of an extended right hepatectomy with segment 4A and cholecystectomy.

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