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Cell experience hairy leukemia patient

Hairy cell leukemia is a rare chronic B-cell disorder that follows an indolent but progressive course. This disorder is characterized by pancytopenia, splenomegaly, bone marrow fibrosis and the presence of atypical lymphoid cells with hairy projections in peripheral blood, bone marrow and spleen. Various parameters such as clinical features, laboratory parameters including complete blood cell count, bone marrow findings, cytochemistry, immunophenotyping by flowcytometry or immunohistochemistry, treatment protocol and complications secondary to treatment and relapse were reviewed. A total of 35 cases were diagnosed during this period of 12 years of which 27 received cladribine and went in to remission.
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Update on the Biology and Treatment Options for Hairy Cell Leukemia

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Hairy cell leukemia: A decade long experience of North Indian Hematology Center

We aimed to analyze the characteristics and response rates of different treatment modalities in hairy cell leukemia patients over 20 diagnosed as hairy cell leukemia HCL. Clinical data, response rates and survival outcome of the patients who were diagnosed with HCL were retrospectively analyzed. Fifty-two patients with a median age of 50 28—87 years were enrolled in the study. First line therapy was cladrabine in 36 patients CR and PR rates were
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Hairy cell leukemia: A decade long experience of North Indian Hematology Center

Hairy cell leukemia HCL is an uncommon chronic B-cell lymphoid malignancy. HCL is differentiated from other B-cell lymphoproliferative disorders by specific cytomorphological, immunophenotypic, and molecular features. In , Bouroncle et al.
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Stories are powerful. Through these stories, we hope you might have a better understanding of what to expect when you are diagnosed, relapse or receive treatment for hairy cell leukemia. Every patient is unique, so the stories you read here might mirror your experience or look and feel different from your own.
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