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Primitive Neuroectodermal Tumor of the Liver in a 13-year-old Boy: A Case Report / 대한소아소화기영양학회지
Article in Korean | WPRIM (Western Pacific) | ID: wpr-130307
Responsible library: WPRO
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.
Subject(s)

Full text: Available Database: WPRIM (Western Pacific) Main subject: Prognosis / Biopsy / Immunohistochemistry / Abdominal Pain / Neuroectodermal Tumors, Primitive / Rare Diseases / Diagnosis, Differential / Fever / Granuloma, Plasma Cell / Liver Type of study: Diagnostic study / Prognostic study Limits: Adolescent / Humans Language: Korean Journal: Korean Journal of Pediatric Gastroenterology and Nutrition Year: 2008 Document type: Article
Full text: Available Database: WPRIM (Western Pacific) Main subject: Prognosis / Biopsy / Immunohistochemistry / Abdominal Pain / Neuroectodermal Tumors, Primitive / Rare Diseases / Diagnosis, Differential / Fever / Granuloma, Plasma Cell / Liver Type of study: Diagnostic study / Prognostic study Limits: Adolescent / Humans Language: Korean Journal: Korean Journal of Pediatric Gastroenterology and Nutrition Year: 2008 Document type: Article
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