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Abstract cute lymphoblastic leukemia (ALL) is a malignant disorder that originates from single B or T lymphoid cells at an early stage of proliferation with accumulation of blast cells in the marrow result in suppression of the hematopoiesis and thereafter the presence of anemia, thrombocytopenia and neutropenia(Sherry, 2007andJalali et al., 2012). Thrombo-embolism (TE) is a well recognized serious complication associated with ALL with potential impact on overall outcome regarding mortality and morbidity and subsequently quality of life (Rau et al., 2007and Jalali et al., 2012). Acute lymphoblastic leukemia is the most common childhood malignancy as associated with various coagulation abnormalities such as hemorrhage and thrombosis. The reported incidence of TE in childhood ALL varies from 1.1% to 36.7% (Stefana et al., 2011). The wide variation in the reported incidence of TE seems to be related to the definition of TE (symptomatic versus asymptomatic), diagnostic method used for detection of TE, study design (prospective versus retrospective) and treatment protocol (Ulrike et al., 2009). The majority of symptomatic TE in children with ALL is venous and 5% of patients were reported to have multiple sites involved. Thromboembolism of CNS occurs in 66% of cases, DVT |