Abdelaziz Khalloufi

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M López-Escobar, M Drake-Monfort, R Salesa-Gutiérrez de Rozas, and S Hermana-Ramírez Servicio de Dermatología, Servicio de Microbiología, and Servicio de Anatomía Patológica, Hospital Universitario Marqués de Valdecilla, Santander, Cantabria, Spain white card. We selected the macro function in the digital camera, switched off the flash, and turned on the(More)
An increase in the number of cases of cutaneous leishmaniasis has been observed, in recent years, in Morocco. We tried, through a series of 49 cases collected from the dermatology department at the military hospital Moulay Ismail of Meknes, to clarify the epidemiological, clinical and evolutionary aspects of the reported cases. We recorded for each patient:(More)
Acquired amegakaryocytic thrombocytopenic purpura is a very rare condition characterized by severe thrombocytopenia linked to the reduction or disappearance of megakaryocytes in the bone marrow. It may be primary idiopathic or secondary to many pathological conditions including hematologic disorders. We report the case of a 24-year-old patient admitted for(More)
Prolymphocytic leukemia T (PLL-T) is a rare entity of mature lymphoproliferative syndrome, characterized by its evolution but especially by its poor prognosis. It is usually revealed by hyperlymphocytosis in the blood. We report a case of prolymphocytic leukemia T, revealed by blood hyperlymphocytosis higher than 800 G/L, diagnosed at the My Ismail military(More)
Plasma cell leukemia (PCL) is a rare and aggressive plasma cell neoplasm that may either originate de novo (primary PCL) or by leukemic transformation of multiple myeloma (MM) to secondary PCL (sPCL). It is defined by the presence of >2 G/L plasma cells or >20% plasmacytosis of the differential white cell count in the peripheral blood. In this case series,(More)
Observation Un soldat âgé de 40 ans, rentré au Maroc depuis un mois après un séjour de dix-huit mois à la République démocratique du Congo, a consulté aux urgences pour une sensation de corps étranger mobile au niveau de l'œil droit, accompagnée d'irritation et de larmoiement. L'examen clinique a objectivé la présence d'un ver mobile sous la conjonctive(More)
Résumé Le purpura thrombopénique amégacaryocytaire acquis est une pathologie très rare caractérisé par une thrombopénie sévère liée une réduction ou une disparition des mégacaryocytes au niveau de la moelle osseuse. Il peut être primaire idiopathique ou secondaire à de nombreux états pathologique dont des hémopathies. Nous rapportons le cas d'un patient de(More)
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