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Two cases of mycosis fungoides with large cell transformation with KMT2A rearrangements.
Wadsworth, Paul A; Lawrence, Lauren; Suarez, Carlos J; Saleem, Atif; Khodadoust, Michael S; Kim, Youn H; Rieger, Kerri E; Fernandez-Pol, Sebastian.
  • Wadsworth PA; Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA, 94305, USA.
  • Lawrence L; Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA, 94305, USA.
  • Suarez CJ; Guardant Health, Redwood City, CA, 94063, USA.
  • Saleem A; Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA, 94305, USA.
  • Khodadoust MS; Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA, 94305, USA.
  • Kim YH; Department of Medicine, Stanford University School of Medicine, Stanford, CA, 94305, USA.
  • Rieger KE; Department of Dermatology, Stanford University School of Medicine, Stanford, CA, 94305, USA.
  • Fernandez-Pol S; Department of Pathology, Stanford University School of Medicine, 300 Pasteur Drive, Stanford, CA, 94305, USA.
J Hematop ; 16(4): 227-234, 2023 Dec.
Article en En | MEDLINE | ID: mdl-38175436
ABSTRACT
Cutaneous T-cell lymphomas (CTCL) are a clinically and molecularly heterogeneous class of lymphomas of the skin-homing T cell, and their genetic profiles are not fully characterized. Previously, rearrangements of the Lysine Methyltransferase 2A (KMT2A) gene have been identified as driver mutations only in acute leukemias. KMT2A plays a role in epigenetic regulation, and cancers with such rearrangements are responsive to epigenetic therapy including hypomethylating agents. Here, we report two cases of CTCL with novel genetic profiles. KMT2A rearrangements were identified in two aggressive cases of mycosis fungoides with large cell transformation. A KMT2ADSCAML1 gene rearrangement was seen in Case 1, while a KMT2AMAPRE1 fusion was identified in Case 2. These cases demonstrate that KMT2A rearrangements can be found in primary CTCLs rather than solely acute leukemias, illustrating the importance of correlating molecular findings with clinical and histologic features in diagnosis. Additionally, this finding suggests that the subset of CTCLs driven by aberrancy of the KMT2A pathway may be responsive to therapy with hypomethylating agents or menin inhibitors, as seen in acute leukemias.
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Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Leucemia / Linfoma Cutáneo de Células T / Micosis Fungoide Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article

Texto completo: 1 Banco de datos: MEDLINE Asunto principal: Neoplasias Cutáneas / Leucemia / Linfoma Cutáneo de Células T / Micosis Fungoide Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Humans Idioma: En Año: 2023 Tipo del documento: Article