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Ann Biol Clin (Paris) ; 79(6): 597-602, 2021 Dec 01.
Artigo em Francês | MEDLINE | ID: mdl-34961740

RESUMO

Large granular lymphocyte leukemia (LGL) constitutes a heterogeneous entity with very different immunophenotypic, clonal and evolutionary characteristics. The most common LGL-T are CD3 +, CD8 +, CD16 +, CD57 +, CD56-. The majority of patients have a chronic disease, systemic signs are rare, and symptoms mainly result from neutropenia or associated autoimmune diseases. We report here a very special case of a 44-year-old woman patient diagnosed with aggressive LGL-T variant also expressing CD56.


Assuntos
Doenças Autoimunes , Leucemia Linfocítica Granular Grande , Adulto , Contagem de Células , Feminino , Humanos , Imunofenotipagem , Leucemia Linfocítica Granular Grande/diagnóstico , Linfócitos
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