作者: E. Renji , A. K. Nathan , M. A. Dalzell
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摘要: A 12-year-old girl with Smith-Lemli-Opitz syndrome and gastrostomy dependency presented multiple episodes of coffee ground vomits. An upper gastrointestinal endoscopy revealed a trichobezoar in the lower oesophagus, ‘hidden treasure’—a retained end G tube at core. Endoscopic retrieval led to resolution symptoms. Literature is scant only one previous report an oesophageal trichobezoar. Techniques removal percutaneous endoscopic children are reviewed. The pathogenesis, preventative measures management for trichobezoars discussed.