Saudi Journal of Pathology and Microbiology (SJPM)
Volume-2 | Issue-03 | 66-69
Case Report
A cause of hyperlymphocytosis exceeding 800 G/L: Prolymphocytic leukemia T (PLL-T).
Dr. Hanane Khalki, Abdelaziz Khalloufi, Hicham Eddou, Dr. Amadou Djibrilla, Amal Taghouti, Imane Tlamçani, Moncef Hassani Amrani
Published : March 30, 2017
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.
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