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Indian J Pathol Microbiol ; 2011 Jul-Sept 54(3): 597-598
Article in English | IMSEAR | ID: sea-142054

ABSTRACT

Sickle cell/beta 0 -thalassemia (S/β0 -thal) is a compound heterozygous state for βS and β0 thalassemia. There are rare reported cases of patients with sickle cell disease who developed hematological neoplasms including myeloid and lymphoid conditions; however, to the best of our knowledge, chronic myelogenous leukemia (CML) occurring in S/β0 -thal has been reported in one case and this is the second such report.


Subject(s)
Adolescent , Anemia, Sickle Cell/complications , Blood Cells/cytology , Bone Marrow/pathology , Female , Histocytochemistry , Humans , Leukemia, Myelogenous, Chronic, BCR-ABL Positive/diagnosis , Leukemia, Myelogenous, Chronic, BCR-ABL Positive/pathology , Microscopy , beta-Thalassemia/complications
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