Gastrointestinal Neuroendocrine Tumors in Two Children
Enterochromaffin-like cell hyperplasia and neuroendocrine tumors are relatively rare in childhood. 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 i...
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Veröffentlicht in: | Indian pediatrics 2016-01, Vol.53 (1), p.70-72 |
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Hauptverfasser: | , , , |
Format: | Artikel |
Sprache: | eng |
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Zusammenfassung: | Enterochromaffin-like cell hyperplasia and neuroendocrine tumors are relatively rare in childhood.
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.
Enterochromaffin-like cell hyperplasia in Case 1 and neuroendocrine tumor in Case 2.
A low index of suspicion for neuroendocrine tumors in children can result in delay in the detection of these rare but potentially malignant diseases. |
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ISSN: | 0974-7559 |
DOI: | 10.1007/s13312-016-0924-y |