Zobrazeno 1 - 10
of 13
pro vyhledávání: '"Philippe Aucher"'
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:
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:
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:
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:
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
Autor:
Franck Lellouche, Philippe Aucher, Pierre Frédéric Augereau, Guillaume Vignon, François Carrere, Sébastien Aubrit, Philippe Mottaz
Publikováno v:
Hématologie. 21:289-294
Nous rapportons l’observation, tres rarement decrite, d’un satellitisme plaquettaire perilymphocytaire apres prelevement sur tube EDTA, ayant permis le diagnostic de lymphome B CD5-. Contrairement au satellitisme entourant les polynucleaires neut
Autor:
Philippe Aucher, François Carrere, Anne Sophie Cognée, Isabelle Masson, Franck Lellouche, Pierre Frédéric Augereau, Florence Borde, Guillaume Vignon
Publikováno v:
Annales de biologie clinique. 75(4)
IgE myeloma is an extremely rare disease characterized by frequent plasma cell leukemia, little monoclonal-spike on electrophoresis, an high incidence of t(11;14) translocation and a worse survival than those with common myelomas. We report here a ne