A cause of hyperlymphocytosis exceeding 800 G/L: Prolymphocytic leukemia T (PLL-T).
Journal Title: Saudi Journal of Pathology and Microbiology - Year 2017, Vol 2, Issue 3
Abstract
Abstract: 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 hospital of Meknès, Morocco. Keywords: Prolymphocyte leukemia, hyperlymphocytosis, immunophenotyping.
Authors and Affiliations
Hanane Khalki, Abdelaziz Khalloufi, Hicham Eddou, Amadou Djibrilla, Amal Taghouti, Imane Tlamçani, Moncef Hassani Amrani
Keywords
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