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首页> 外文期刊>Medicine. >A 4 and a half years old boy with mesenchymal hamartomas in the left lateral lobe of the liver: A case report and literature review
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A 4 and a half years old boy with mesenchymal hamartomas in the left lateral lobe of the liver: A case report and literature review

机译:一个4岁半肝左叶间质错构瘤的男孩:一例病例并文献复习

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Rationale: Mesenchymal hamartomas of the liver is one type of rare liver tumor. Patient concerns: Mesenchymal hamartomas of the liver (MHL) is rarely reported in the left lobe of the liver in children who are more than 2 years old. It is difficult to distinguish it from liver lesions such as hepatoblastoma in children, and hepatocellular carcinoma and focal nodular hyperplasia in adults. In addition, it is hard to correctly diagnose it without pathological examination. Diagnoses: Mesenchymal hamartomas of the liver. Interventions: This patient underwent an operation assisted by the Da Vinci surgical system and the tumor was completely resected. Outcomes: No tumor recurrence or metastasis was observed 14 months after operation. Lessons: MHL is a benign tumor that is difficult to diagnose due to the lack of specific clinical symptoms and signs. The management of MHL remains controversial. To achieve a good long-term outcome, complete resection of MHL is recommended.
机译:理由:肝间质错构瘤是一种罕见的肝肿瘤。患者关注:2岁以上儿童的肝左叶很少报道间质肝错构瘤(MHL)。很难将其与儿童肝病如肝母细胞瘤,成人肝细胞癌和局灶性结节性增生区分开。另外,不进行病理检查就很难正确诊断。诊断:肝间质错构瘤。干预措施:该患者在达芬奇外科手术系统的辅助下进行了手术,肿瘤被完全切除。结果:术后14个月未观察到肿瘤复发或转移。经验教训:MHL是一种良性肿瘤,由于缺乏特定的临床症状和体征而难以诊断。 MHL的管理仍存在争议。为了获得良好的长期结果,建议完全切除MHL。

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