Zobrazeno 1 - 10
of 16
pro vyhledávání: '"Guillaume Vignon"'
Autor:
Guillaume Vignon, Annick Boscagli, Julien Labrousse, Anthony Bonnin, Adrian Hij, François Carrere, Pierre-Frédéric Augereau, Philippe Aucher, Franck Lellouche
Publikováno v:
Hématologie. 28:217-230
Autor:
Emmanuelle Bonnin, Guillaume Vignon, Adrian Hij, Alexandre Saunier, Franck Lellouche, Claire Montrieul
Publikováno v:
Hématologie. 27:32-39
Autor:
François Carrere, Philippe Aucher, Julien Labrousse, Annick Boscagly, Adrian Hij, Franck Lellouche, Guillaume Vignon, Pierre-Frédéric Augereau, Anthony Bonnin
Publikováno v:
Annales de biologie clinique. 79(5)
During a blood test, the discovery of thrombocytosis is a frequent phenomenon with multiple origins. False thrombocytosis linked to analytical interferences is rare but must be eliminated before confirming the anomaly. The reaction origin, often very
Autor:
Pierre-Frédéric Augereau, François Carrere, Guillaume Vignon, Anthony Bonnin, Philippe Aucher, Julien Labrousse, Franck Lellouche, Sophie Pasini, Philippe Mottaz
Publikováno v:
Hématologie. 25:286-297
The discovery of a monocytosis is a frequent phenomenon, requiring confirmation by reading under a microscope by an experimented biologist, to overcome usual cytological traps such as the presence of hairy cells, promonocytes or monoblasts. In the va
Autor:
Julien Labrousse, Guillaume Vignon, François Carrere, Pierre-Frédéric Augereau, Anne Sophie Meunier, Franck Lellouche, Philippe Aucher, Adrian Hij
Publikováno v:
Annales de biologie clinique. 79(1)
Sideroblastic anemias in adults are often quickly labeled as myelodysplasias. We report two unfrequent observations of secondary acquired forms. The first one is a 15-year-old girl presented with severe cytopenias. The myelogram revealed the presence
Autor:
Anthony Bonnin, Pierre-Frédéric Augereau, Florent Plasse, Philippe Mottaz, Phlippe Aucher, Julien Labrousse, Franck Lellouche, Guillaume Vignon, François Carrere
Publikováno v:
Annales de biologie clinique. 78(1)
Immunosuppression is a well known risk factor for the development of lymphoid pathologies. The classification of these neoplasias is becoming more precise and complex, some features being common to all immunocompromised patients, primarily the import
Autor:
Franck Lellouche, Sophie Pasini, Florent Plasse, François Carrere, Philippe Mottaz, Philippe Aucher, Guillaume Vignon, Pierre-Frédéric Augereau, Anthony Bonnin
Publikováno v:
Annales de biologie clinique. 77(3)
The etiological assessment of a monoclonal gammopathy is currently standardized, the decisional algorithms allowing a sufficiently precise classification to consider the care, wait or therapeutic. The purpose of this review is to recall the difficult
Autor:
Julien Labrousse, Franck Lellouche, François Carrere, Pierre Frédéric Augereau, Philippe Mottaz, Philippe Aucher, Guillaume Vignon, Anthony Bonnin
Publikováno v:
Annales de biologie clinique. 76(6)
Adult neutropenia, defined as a blood neutrophil count below 1.5 G/L, is a common condition. The most common cause of acute neutropenia is a drug-related reaction or an acute infectious disease. In chronic forms many etiologies are possible, sometime
Autor:
Guillaume, Vignon, Roxane, Jeanneau, Julien, Labrousse, Sébastien, Aubrit, Philippe, Mottaz, François, Carrère, Pierre-Frédéric, Augereau, Philippe, Aucher, Franck, Lellouche
Publikováno v:
Annales de biologie clinique. 76(5)
The most frequent causes of hemolytic anemias are immune or infectious diseases, drug induced hemolysis, thrombotic microangiopathies, hereditary spherocytosis, glucose-6-phosphate dehydrogenase or pyruvate kinase deficiencies, thalassemia's and sick
Autor:
Julien, Labrousse, Florent, Plasse, Philippe, Aucher, Pierre, Augereau, Anne, Bertin, François, Carrere, Anne-Sophie, Cognée, Guillaume, Vignon, Jérémie, Violette, Franck, Lellouche
Publikováno v:
Annales de biologie clinique. 76(5)
The presence of serum monoclonal IgM is often associated with the diagnosis of Waldenström macroglobulinemia (WM) or other chronic lymphoproliferative disorders. IgM myeloma is a rare entity (0.5%). We report the case of an IgM myeloma complicated b