Gastrointestinal Neuroendocrine Tumors in Two Children

被引：0
|
作者：
Koca, Tugba [1 ]
Dereci, Selim [1 ]
Karahan, Nermin [2 ]
Akcam, Mustafa [1 ]
机构：
[1] Suleyman Demirel Univ, Fac Med, Dept Pediat, Div Pediat Gastroenterol Hepatol & Nutr, TR-32200 Isparta, Turkey
[2] Suleyman Demirel Univ, Fac Med, Dept Pathol, TR-32200 Isparta, Turkey
来源：
INDIAN PEDIATRICS | 2016年 / 53卷 / 01期
关键词：
Abdominal pain; H; pylori; Hemtochezia; GASTRITIS; COLON;
D O I：
暂无
中图分类号：
R72 [儿科学];
学科分类号：
100202 ;
摘要：
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.
引用
收藏
页码：70 / 72
页数：3
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