Gastrointestinal stromal tumor (GIST) usually originates from the cells of the stomach wall or small intestinal wall. Gastrointestinal stromal tumor can be benign or malignant (cancer). Pediatric gastrointestinal stromal tumor is more common in girls and adolescents.
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The characteristics of gastrointestinal stromal tumors in children are significantly different from those in adults, and tumor gene mutation testing must be performed. A small number of pediatric patients have the same genetic mutations as adult patients.
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The following genetic disorders may increase the risk of gastrointestinal stromal tumors:
Gastrointestinal stromal tumor signs also include: abdominal mass or intestinal obstruction (abdominal spasmodic pain, nausea, vomiting, diarrhea, constipation, and bloating). Anemia caused by other conditions may also cause the same symptoms.
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For the treatment information below, see the treatment plan overview section above.
Children with the same genetic mutation as adult patients were treated with targeted therapy with tyrosine kinase inhibitors.
Children without genetic mutations can be exposed to the tumor through surgery.
Children with recurrent gastrointestinal stromal tumors may be considered for clinical trials to test whether the genes in the patient's tumor samples have changed and to target the patient based on the type of gene change.
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