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Redefining the high-grade B cell lymphoma with double/triple rearrangements of MYC and BCL2/BCL6 genes. Learning from a case report.
Rodríguez-Pinilla, Socorro María; Salgado, Rocío Nieves; Chamizo, Cristina; Santonja, Carlos; Stewart, Peter; Carvajal, Nerea; McCafferty, Neil; Manso, Rebeca; Morillo, Daniel; Piris, Miguel Ángel; González de Castro, David.
Afiliación
  • Rodríguez-Pinilla SM; Pathology Department Hospital Universitario Fundación Jiménez Díaz (FJD) Madrid Spain.
  • Salgado RN; Cytogenetic Department Hospital Universitario Fundación Jiménez Díaz (FJD) Madrid Spain.
  • Chamizo C; Pathology Department Hospital Universitario Fundación Jiménez Díaz (FJD) Madrid Spain.
  • Santonja C; Pathology Department Hospital Universitario Fundación Jiménez Díaz (FJD) Madrid Spain.
  • Stewart P; Patrick G Johnston Centre for Cancer Research Queen's University Belfast Belfast UK.
  • Carvajal N; Pathology Department Hospital Universitario Fundación Jiménez Díaz (FJD) Madrid Spain.
  • McCafferty N; Patrick G Johnston Centre for Cancer Research Queen's University Belfast Belfast UK.
  • Manso R; Pathology Department Hospital Universitario Fundación Jiménez Díaz (FJD) Madrid Spain.
  • Morillo D; Haematology Department Hospital Universitario Fundación Jiménez Díaz Madrid Spain.
  • Piris MÁ; Pathology Department Hospital Universitario Fundación Jiménez Díaz (FJD) Madrid Spain.
  • González de Castro D; Patrick G Johnston Centre for Cancer Research Queen's University Belfast Belfast UK.
EJHaem ; 3(1): 171-174, 2022 Feb.
Article en En | MEDLINE | ID: mdl-35846201
We report a patient initially diagnosed with a triple hit high-grade B cell lymphoma (HGBL-TH), in which further morphologic, immunohistochemical, and next-generation sequencing studies of subsequent specimens disclosed it to be a germinal center diffuse large B cell lymphoma (GC-DLBCL) with BCL2/BCL6 gene translocations, PVT1-deletion, and gain of MYC genes evolving from a previous follicular lymphoma. However, fluorescence in situ hybridization (FISH) studies with the break-apart probe for MYC gene showed a fusion and two separated signals (red and green, respectively) leading to the interpretation of MYC gene translocation and a false diagnosis of a TH-lymphoma, according to the recent WHO classification. Nevertheless, PVT1 deletion plus MYC gain/amplification has been described as a cause of the double-hi transcription profile. These data highlight the need for new criteria to identify these highly aggressive lymphomas.
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Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: EJHaem Año: 2022 Tipo del documento: Article

Texto completo: 1 Colección: 01-internacional Base de datos: MEDLINE Tipo de estudio: Prognostic_studies Idioma: En Revista: EJHaem Año: 2022 Tipo del documento: Article
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