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Updated: Jun 4, 2026

Robotic Duodenal Sleeve Resection for Gastrointestinal Stromal Tumor with Rare Exon 8 KIT Mutation Following Neoadjuvant Imatinib
Published on: April 3, 2026
A rare cause of intestinal obstruction: neonatal gastrointestinal stromal tumor
Bilge Tanyeri1, Naim Koku, Mustafa Demirci
1Department of Neonatology, Bezmialem University Faculty of Medicine, Istanbul, Turkey. tanyeribilge@yahoo.com
Abstract:
Gastrointestinal stromal tumors (GISTs) are rare in the childhood period. The authors reported a case who was admitted to the neonatal intensive care unit (NICU) on a suspicion of intestinal obstruction. She was operated and a mass in a size of 6 x 4.5 x 4 cm was resected from the ileum. Histologic and immunohistochemical studies showed a GIST. CD34, small muscle actin (SMA), and desmin were positive. The baby was discharged on the 13th day after operation.
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