ALK rearrangements in infantile fibrosarcoma‐like spindle cell tumours of soft tissue and kidney

Author:

Tan Serena Y1ORCID,Al‐Ibraheemi Alyaa2ORCID,Ahrens William A3,Oesterheld Javier E4,Fanburg‐Smith Julie C5,Liu Yajuan J6,Spunt Sheri L7,Rudzinski Erin R8,Coffin Cheryl9,Davis Jessica L10ORCID

Affiliation:

1. Department of Pathology Stanford University School of Medicine Palo Alto CAUSA

2. Department of Pathology Boston Children’s Hospital and Harvard Medical School Boston MAUSA

3. Department of Pathology Atrium HealthCharlotte NCUSA

4. Department of Pediatrics Levine Children’s Hospital Atrium Health Charlotte NCUSA

5. Department of Pathology, Pediatrics and Orthopedics PennState Health Penn State Children’s Hospital Penn State College of Medicine Hershey PAUSA

6. Department of Laboratory Medicine and Pathology University of Washington School of Medicine Seattle WAUSA

7. Department of Pediatrics Stanford University School of Medicine Palo Alto CAUSA

8. Department of Laboratories Seattle Children’s Hospital Seattle WAUSA

9. Department of Pathology, Microbiology, and Immunology Vanderbilt University Nashville TNUSA

10. Department of Pathology Oregon Health & Sciences University Portland OR USA

Publisher

Wiley

Subject

General Medicine,Histology,Pathology and Forensic Medicine

Reference64 articles.

1. Nonrandom numerical chromosome aberrations (+8, +11, +17, +20) in infantile fibrosarcoma;Mandahl N;Cancer Genet. Cytogenet.,1989

2. Congenital mesoblastic nephroma t(12;15) is associated with ETV6–NTRK3 gene fusion;Rubin BP;Am. J. Pathol.,1998

3. ETV6–NTRK3 gene fusions and trisomy 11 establish a histogenetic link between mesoblastic nephroma and congenital fibrosarcoma;Knezevtch SR;Cancer Res.,1998

4. Molecular detection of the ETV6–NTRK3 gene fusion differentiates congenital fibrosarcoma from other childhood spindle cell tumors;Bourgeois JM;Am. J. Surg. Pathol.,2000

5. Identification of NTRK fusions in pediatric mesenchymal tumors;Pavlick D;Pediatr. Blood Cancer,2017

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