Primary cutaneous gamma/delta T‐cell lymphoma with simultaneous JAK2 and TP63 rearrangements: a new double‐hit?
Author:
Affiliation:
1. Department of Laboratory Medicine and Pathology Mayo Clinic Rochester MN USA
2. Division of Hematology Mayo Clinic Rochester MN USA
3. Department of Dermatology Mayo Clinic Rochester MN USA
Funder
National Institutes of Health
Publisher
Wiley
Subject
General Medicine,Histology,Pathology and Forensic Medicine
Link
https://onlinelibrary.wiley.com/doi/pdf/10.1111/his.14973
Reference7 articles.
1. Cellular origins and genetic landscape of cutaneous gamma delta T cell lymphomas
2. Recurrent STAT3-JAK2 fusions in indolent T-cell lymphoproliferative disorder of the gastrointestinal tract
3. Genome-wide analysis reveals recurrent structural abnormalities of TP63 and other p53-related genes in peripheral T-cell lymphomas
4. t(8;9)(p22;p24)/PCM1-JAK2 Activates SOCS2 and SOCS3 via STAT5
5. A phase 2 biomarker-driven study of ruxolitinib demonstrates effectiveness of JAK/STAT targeting in T-cell lymphomas
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1. A Rare Case of Primary Cutaneous Gamma-Delta T-cell Lymphoma with Aberrant B-cell Marker Expression;The American Journal of Dermatopathology;2023-11
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