Concomitant MDS with isolated 5q deletion and MGUS: case report and review of molecular aspects.

Nolte, Florian; Mossner, Maximilian; Jann, Johann-Christoph; Nowak, Daniel; Boch, Tobias; Müller, Nadine Zoe; Hofmann, Wolf-Karsten; Metzgeroth, Georgia

Nolte, Florian; Mossner, Maximilian; Jann, Johann-Christoph; Nowak, Daniel; Boch, Tobias; Müller, Nadine Zoe; Hofmann, Wolf-Karsten; Metzgeroth, Georgia.

Afiliação

Nolte F; Medical faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Mossner M; Department of Internal Medicine, Hematology and Oncology, St. Hedwig Hospital, Berlin, Germany.
Jann JC; Medical faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Nowak D; Medical faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Boch T; Medical faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Müller NZ; Department of Hematology and Oncology, University Hospital Mannheim, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Hofmann WK; Medical faculty Mannheim of the University of Heidelberg, Mannheim, Germany.
Metzgeroth G; Department of Hematology and Oncology, University Hospital Mannheim, Medical Faculty Mannheim of the University of Heidelberg, Mannheim, Germany.

Eur J Haematol ; 98(3): 302-310, 2017 Mar.

Article em En | MEDLINE | ID: mdl-27862375

Assuntos

Deleção Cromossômica; Cromossomos Humanos Par 5; Gamopatia Monoclonal de Significância Indeterminada/diagnóstico; Gamopatia Monoclonal de Significância Indeterminada/genética; Síndromes Mielodisplásicas/diagnóstico; Síndromes Mielodisplásicas/genética; Idoso; Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico; Medula Óssea/patologia; Progressão da Doença; Humanos; Leucemia Mieloide Aguda/diagnóstico; Leucemia Mieloide Aguda/genética; Masculino; Gamopatia Monoclonal de Significância Indeterminada/terapia; Mutação; Síndromes Mielodisplásicas/tratamento farmacológico; Proteínas Repressoras/genética

Palavras-chave

hematopoiesis and hematopathology; multiple myeloma; myelodysplastic syndromes; stem cell biology

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Texto completo: 1 Base de dados: MEDLINE Assunto principal: Síndromes Mielodisplásicas / Cromossomos Humanos Par 5 / Gamopatia Monoclonal de Significância Indeterminada / Deleção Cromossômica Tipo de estudo: Diagnostic_studies Limite: Aged / Humans / Male Idioma: En Ano de publicação: 2017 Tipo de documento: Article

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