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J T Xu1, L B Fu1, X F Yao1

  • 1Department of Pathology, Beijing Children's Hospital, Capital Medical University, National Center for Children's Health, Beijing 100045, China.

概括

先天性脊柱细胞/硬化性拉布多米索尔科马是一种罕见的婴儿拉布多米索尔科马亚型,通常出现在胸部或背部. NCOA2 / VGLL2基因融合是常见的,其预后通常比其他类型的狂宫肌肉瘤更好.