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Gastrointestinal Neuroendocrine Tumors in Two Children

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dc.creator Dereci, Selim
dc.creator Koca, Tugba
dc.creator KARAHAN, Nermin
dc.creator AKÇAM, Mustafa
dc.date 2015-12-31T22:00:00Z
dc.date.accessioned 2020-10-06T10:31:21Z
dc.date.available 2020-10-06T10:31:21Z
dc.identifier 6c1a19c7-4b26-424c-b046-685dc271eefe
dc.identifier 10.1007/s13312-016-0924-y
dc.identifier https://avesis.sdu.edu.tr/publication/details/6c1a19c7-4b26-424c-b046-685dc271eefe/oai
dc.identifier.uri http://acikerisim.sdu.edu.tr/xmlui/handle/123456789/62723
dc.description Background: Enterochromaffin-like cell hyperplasia and neuroendocrine tumors are relatively rare in childhood. Case characteristics: A 15-year-old girl who presented with epigastric pain and a 6-year-old boy who was admitted with hematochezia. Endoscopy revealed nodules in the stomach in Case 1, and polyploidy lesion in the rectum in Case 2. Outcome: Enterochromaffin-like cell hyperplasia in Case 1 and neuroendocrine tumor in Case 2. Message: A low index of suspicion for neuroendocrine tumors in children can result in delay in the detection of these rare but potentially malignant diseases.
dc.language eng
dc.rights info:eu-repo/semantics/closedAccess
dc.title Gastrointestinal Neuroendocrine Tumors in Two Children
dc.type info:eu-repo/semantics/article


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