Lack of classical astroblastoma features in pediatric MN1::BEND2-fused brain tumors.

• Tác giả: Nicholas Chapman, Jennifer A Cotter, Tom Belle Davidson, Debra Hawes, Mohammed Iqbal, Jianling Ji, Mark D Krieger, Nathan Robison, Benita Tamrazi, Adam D Walker
• Ngôn ngữ: eng
• Ký hiệu phân loại: 770.11 Inherent features
• Thông tin xuất bản: Switzerland : Brain pathology (Zurich, Switzerland) , 2025
• Bộ sưu tập: NCBI
• ID: 188633

Tóm tắt

Three distinct MN1::BEND2 fusion-positive tumors in pediatric patients. (A) Clinical course for each patient was variable in part due to differences in initial diagnosis. Each patient responded favorably to gross total resection and is stable at last follow-up. (B) Histologic diversity, lack of prominent classical astroblastoma features, and variable immunoexpression of key markers makes microscopic diagnosis challenging.