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      Congenital mesoblastic nephroma is characterised by kinase mutations including EGFR internal tandem duplications, the ETV6-NTRK3 fusion, and the rare KLHL7-BRAF fusion.

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          Abstract

          Congenital mesoblastic nephroma (CMN) is histologically classified into classic, cellular and mixed subtypes. The aims of this study were to characterise the clinical, pathological and molecular features of a series of CMNs, and to determine the utility of pan-Trk and epidermal growth factor receptor (EGFR) immunohistochemistry as surrogate markers for NTRK gene fusions and EGFR internal tandem duplications (ITDs).

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          Author and article information

          Journal
          Histopathology
          Histopathology
          Wiley
          1365-2559
          0309-0167
          Oct 2020
          : 77
          : 4
          Affiliations
          [1 ] Department of Pathology, The Children's Hospital, Zhejiang University School of Medicine, National Clinical Research Center for Child Health, Hangzhou, Zhejiang Province, China.
          [2 ] Department of Pathology, Shanghai Children's Medical Centre, Shanghai, China.
          [3 ] Department of Pathology and Laboratory Medicine, KK Women's and Children's Hospital, Singapore.
          [4 ] Lady Ridgeway Hospital for Children, Colombo, Sri Lanka.
          [5 ] Department of Paediatric Surgery, KK Women's and Children's Hospital.
          [6 ] Duke-NUS Medical School, Singapore.
          Article
          10.1111/his.14194
          32590884
          4e764357-6360-4d8a-84ce-cfc8e3abbcc2
          History

          EGFR immunohistochemistry,EGFR internal tandem duplication,KLHL7-BRAF gene fusion,congenital mesoblastic nephroma,pan-Trk immunohistochemistry

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