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Pediatr Dev Pathol ; 24(4): 371-377, 2021.
Article in English | MEDLINE | ID: mdl-33734915

ABSTRACT

Overall, neonatal cancer is uncommon. Because of its rarity and heterogeneity, diagnosis can be challenging. We report a unique case of a myoepithelial carcinoma in a 7 week old girl. Molecular diagnostic workup revealed a EWSR1-KLF15 gene fusion which was previously described in only six cases of myoepithelial tumors so far. All cases occurred in children and adolescents. To our knowledge, this is the first report of a congenital EWSR1-KLF15 fusion positive myoepithelial tumor in an infant.


Subject(s)
Biomarkers, Tumor/genetics , Gene Fusion , Kruppel-Like Transcription Factors/genetics , Myoepithelioma/genetics , RNA-Binding Protein EWS/genetics , Soft Tissue Neoplasms/genetics , Female , Humans , Infant , Myoepithelioma/diagnosis , Myoepithelioma/pathology , Soft Tissue Neoplasms/diagnosis , Soft Tissue Neoplasms/pathology
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