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Establishment and Characterization of Small Bowel Neuroendocrine Tumor Spheroids
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Gastrointestinal Neuroendocrine Tumors in Two Children

Tugba Koca1, Selim Dereci, Nermin Karahan

  • 1Departments of Pediatrics, Division of Pediatric Gastroenterology, Hepatology and Nutrition, and *Department of Pathology; Faculty of Medicine, Suleyman Demirel University, Isparta, Turkey. Correspondence to: Dr Tugba Koca, Department of Pediatrics, Suleyman Demirel University Faculty of Medicine, Cunur, Isparta, Turkey. tgkoca@gmail.com.

Indian Pediatrics
|February 4, 2016
PubMed

Insights

Childhood neuroendocrine tumors (NETs) and related cell hyperplasia are rare. Early detection is crucial, as a low suspicion index can delay diagnosis of these potentially malignant conditions in pediatric patients.

Area of Science:

  • Pediatric Gastroenterology
  • Oncology
  • Endocrinology

Background:

  • Enterochromaffin-like cell hyperplasia and neuroendocrine tumors are uncommon in pediatric populations.
  • These conditions can present with nonspecific gastrointestinal symptoms.
Abstract

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