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Potential role of MAP2K1 mutation in the trans-differentiation of interdigitating dendritic cell sarcoma: Case report and literature review.
Jenei, Alex; Bedics, Gábor; Erdélyi, Dániel J; Müller, Judit; Györke, Tamás; Bödör, Csaba; Szepesi, Ágota.
Afiliação
  • Jenei A; Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
  • Bedics G; Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
  • Erdélyi DJ; Hungarian Centre of Excellence for Molecular Medicine - Semmelweis University (HCEMM-SE) Molecular Oncohematology Research Group, Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
  • Müller J; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Györke T; 2nd Department of Pediatrics, Semmelweis University, Budapest, Hungary.
  • Bödör C; Department of Nuclear Medicine Semmelweis University, Budapest, Hungary.
  • Szepesi Á; Department of Pathology and Experimental Cancer Research, Semmelweis University, Budapest, Hungary.
Front Pediatr ; 10: 959307, 2022.
Article em En | MEDLINE | ID: mdl-36186629
ABSTRACT
A 5-year-old male child was diagnosed with interdigitating dendritic cell sarcoma (IDCS) during his maintenance therapy for B-cell precursor acute lymphoblastic leukemia (B-ALL). Multiplex lymph node involvements of the neck were found by positron emission tomography CT (PET-CT). Treatments, including surgical and chemotherapy, resulted in complete remission. Four years later, systemic bone infiltration was discovered. Surgical resection of the IV rib and intensive chemotherapy led to a complete morphological remission, and allogeneic bone marrow transplantation was performed. Comprehensive genomic profiling of the formalin fixed the tumor tissue, and the cryopreserved leukemic cells revealed several common alterations and divergent clonal evolution with a novel MAP2K1 mutation of the IDCS, which is responsible for the trans-differentiation of the common lymphoid-committed tumor progenitor.
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Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article

Texto completo: 1 Base de dados: MEDLINE Tipo de estudo: Systematic_reviews Idioma: En Ano de publicação: 2022 Tipo de documento: Article