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Mediastinal Germ Cell Tumor and Acute Megakaryoblastic Leukemia With Co-occurring KRAS Mutation and Complex Cytogenetics.
Amra, Nasir; Zarate, Luis Velasquez; Punia, Jyotinder N; Mahajan, Priya; Stevens, Alexandra M; Roy, Angshumoy; Curry, Choladda V; Cortes-Santiago, Nahir; Fisher, Kevin E.
Afiliação
  • Amra N; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Zarate LV; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Punia JN; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Mahajan P; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Stevens AM; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Roy A; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Curry CV; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Cortes-Santiago N; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
  • Fisher KE; Department of Pathology & Immunology, Baylor College of Medicine, Houston, Texas.
Pediatr Dev Pathol ; 23(6): 461-466, 2020.
Article em En | MEDLINE | ID: mdl-32815783
Young males have a unique but rare predilection to develop mediastinal nonseminomatous germ cell tumors (NSGCTs) and concomitant acute megakaryoblastic leukemia (AMKL). Common cytogenetic and molecular abnormalities such as isochromosome 12p and somatic Tumor Protein P53(TP53) and Phosphatase And Tensin Homolog (PTEN) mutations have been reported in the presumed mutual neoplastic clones of origin. We report the case of a 17-year-old male who presented with a mediastinal NSGCT with high-grade sarcomatous transformation and a diagnosis of AMKL approximately 4 months later. Next-generation sequencing revealed identical KRAS Proto-Oncogene, GTPase (KRAS) p.Ala146Thr, TP53 p.Leu257Pro, and PTEN p.Leu181Pro missense mutations at similar variant allele frequencies in both the NSGCT and AMKL samples. Cytogenetic and microarray analyses detected shared copy gains in all chromosomes except chromosomes 9, 13, and Y. Multiple additional clonal chromosomal alterations were detected in the AMKL sample when compared with the NSGCT. This case emphasizes the shared clonal origins of these malignancies and identifies KRAS and other copy number alterations as potential molecular drivers in a subset of these combined diseases.
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Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Biomarcadores Tumorais / Leucemia Megacarioblástica Aguda / Proteínas Proto-Oncogênicas p21(ras) / Neoplasias Embrionárias de Células Germinativas / Neoplasias do Mediastino Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Humans / Male Idioma: En Revista: Pediatr Dev Pathol Assunto da revista: PATOLOGIA / PEDIATRIA Ano de publicação: 2020 Tipo de documento: Article

Texto completo: 1 Coleções: 01-internacional Base de dados: MEDLINE Assunto principal: Neoplasias Testiculares / Biomarcadores Tumorais / Leucemia Megacarioblástica Aguda / Proteínas Proto-Oncogênicas p21(ras) / Neoplasias Embrionárias de Células Germinativas / Neoplasias do Mediastino Tipo de estudo: Diagnostic_studies / Prognostic_studies Limite: Adolescent / Humans / Male Idioma: En Revista: Pediatr Dev Pathol Assunto da revista: PATOLOGIA / PEDIATRIA Ano de publicação: 2020 Tipo de documento: Article