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Non-Functioning, Malignant Pancreatic Neuroendocrine Tumor in a 16-Year-old Boy: A Case Report
Journal of the Korean Society of Magnetic Resonance in Medicine ; : 145-150, 2010.
Article in English | WPRIM | ID: wpr-198470
ABSTRACT
We report the case of a 16-year-old boy with a solid pancreatic mass which proved to be a nonfunctioning, malignant pancreatic neuroendocrine tumor (PNET). In pediatric patients, malignant pancreatic tumors are rare, especially malignant PNET. When dynamic contrast enhanced MRI showed a well enhancing solid pancreatic tumor on arterial and delayed phases and combined with malignant features, such as vascular invasion, invasion of adjascent organs, and lymphadenopathy, we should include malignant pancreatic neuroendocrine tumor in the differential diagnosis of childhood pancreatic tumors.
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Full text: Available Index: WPRIM (Western Pacific) Main subject: Neuroendocrine Tumors / Neuroectodermal Tumors, Primitive / Adenoma, Islet Cell / Diagnosis, Differential / Lymphatic Diseases Type of study: Diagnostic study Limits: Adolescent / Child / Humans Language: English Journal: Journal of the Korean Society of Magnetic Resonance in Medicine Year: 2010 Type: Article

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Full text: Available Index: WPRIM (Western Pacific) Main subject: Neuroendocrine Tumors / Neuroectodermal Tumors, Primitive / Adenoma, Islet Cell / Diagnosis, Differential / Lymphatic Diseases Type of study: Diagnostic study Limits: Adolescent / Child / Humans Language: English Journal: Journal of the Korean Society of Magnetic Resonance in Medicine Year: 2010 Type: Article