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T-cell lymphoma, B-cell lymphoma, and myelodysplastic syndrome harboring common mutations: Trilineage tumorigenesis from a common founder clone.
Yoshihara, Kyoko; Nannya, Yasuhito; Matsuda, Ikuo; Samori, Mami; Utsunomiya, Nobuto; Okada, Masaya; Hirota, Seiichi; Ogawa, Seishi; Yoshihara, Satoshi.
Afiliação
  • Yoshihara K; Department of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
  • Nannya Y; Department of Pathology and Tumor Biology Kyoto University Kyoto Japan.
  • Matsuda I; Department of Surgical Pathology Hyogo College of Medicine Nishinomiya Japan.
  • Samori M; Department of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
  • Utsunomiya N; Department of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
  • Okada M; Department of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
  • Hirota S; Department of Surgical Pathology Hyogo College of Medicine Nishinomiya Japan.
  • Ogawa S; Department of Pathology and Tumor Biology Kyoto University Kyoto Japan.
  • Yoshihara S; Department of Hematology Hyogo College of Medicine Hospital Nishinomiya Japan.
EJHaem ; 3(1): 211-214, 2022 Feb.
Article em En | MEDLINE | ID: mdl-35846192
ABSTRACT
A 64-year-old man with angioimmunoblastic T-cell lymphoma (AITL) subsequently developed diffuse large B-cell lymphoma (DLBCL) and myelodysplastic syndrome (MDS). Genomic profiling of AITL, DLBCL, and MDS samples revealed that the tumor cells from all samples shared common mutations in TET2 and DNMT3A. In addition, the IDH2 mutation was observed in AITL, and TP53 mutation was observed in DLBCL and MDS. These findings illustrate the clonal relationship between AITL and DLBCL in addition to AITL and MDS, with the latter being increasingly reported. The present findings strongly support the theory of multistep and multilineage tumorigenesis from a common founder clone.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EJHaem Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Idioma: En Revista: EJHaem Ano de publicação: 2022 Tipo de documento: Article