Primitive Neuroectodermal Tumor of the Liver in a 13-year-old Boy: A Case Report

Sang Lee, Ji Eun Kim, Ji Hyuk Lee, H. Lee, Jong Seung Lee, Jee Hyun Lee, Y. Choe
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Abstract

Primary primitive neuroectodermal tumor (PNET) of the liver is a rare disease with aggressive behavior and poor prognosis. We report a case of a PNET of the liver in a 13-year-old boy. The patient was admitted to the hospital with fever and abdominal pain. Abdominal CT and MRI revealed a 5.5 cm sized, septated, non-enhancing mass in the hepatic hilum. The patient was initially diagnosed with an inflammatory pseudotumor. Despite 9 days of antibiotic therapy, the patient’s clinical symptoms did not improve. A liver biopsy was performed in the interest of formulating a differential diagnosis. This procedure revealed tumor cells positive for CD99 on immunohistochemistry. The patient was diagnosed with a PNET. (Korean J Pediatr Gastroenterol Nutr 2008; 11: 214∼218)
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13岁男孩原发性肝脏神经外胚层肿瘤1例报告
肝脏原发性原始神经外胚层肿瘤(PNET)是一种罕见的疾病,具有侵袭性,预后差。我们报告一个13岁男孩的肝脏PNET病例。病人因发烧和腹痛住进医院。腹部CT和MRI显示肝门有一个5.5厘米大小的分隔性无增强肿块。患者最初被诊断为炎性假瘤。经过9天的抗生素治疗,患者的临床症状未见改善。肝活检是在制定鉴别诊断的利益。结果显示肿瘤细胞CD99免疫组化阳性。患者被诊断为PNET。韩国儿科胃肠病学杂志2008;11: 214∼218)
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