ABSTRACT
Pediatric neuroendocrine tumors (NETs) are slow-growing tumors arising from neuroendocrine system and are very rare. Tumors are diagnosed incidentally and may present with vague symptoms, including abdominal pain, weight loss, fatigue, diarrhea and flushing. Early-stage and well-differentiated tumors have excellent outcomes. Complete surgical resection is the only treatment option and curative for most of the cases.
