Recurrent EGFR alterations in NTRK3 fusion negative congenital mesoblastic nephroma

Recurrent EGFR alterations in NTRK3 fusion negative congenital mesoblastic nephroma

Objectives: To identify oncogenic driver mutations in congenital mesoblastic nephroma (CMN) cases lacking ETV6-NTRK3 fusion and discuss their diagnostic value. Design: The institutional pathology database was queried for cases with a morphologic diagnosis of CMN. Cases positive for ETV6 rearrangemen...

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Bibliographic Details
Main Authors: Li Lei, Bradley A. Stohr, Stacey Berry, Christina M. Lockwood, Jessica L. Davis, Erin R. Rudzinski, Christian A. Kunder
Format: Article
Language:English
Published: Elsevier 2020-08-01
Series:Practical Laboratory Medicine
Subjects:
Congenital mesoblastic nephroma
EGFR, kinase domain duplication
ETV6-NTRK3
Online Access:http://www.sciencedirect.com/science/article/pii/S2352551719300952

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http://www.sciencedirect.com/science/article/pii/S2352551719300952

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