Please use this identifier to cite or link to this item: http://148.72.244.84:8080/xmlui/handle/xmlui/5607
Title: Acute Lymphoblastic Leukemia, Classification, Clinical features and Diagnosis
Authors: Fatimah Kadhim Ibrahim AL- Mahdawi
Mazin Razooqi Mohammed
Keywords: Acute Lymphoblastic Leukemia
Blood
Issue Date: Dec-2020
Publisher: University of Diyala - College of Medicine
Citation: https://doi.org/10.26505/DJM.19025390602
Series/Report no.: Vol 19;Issue 2
Abstract: Background: Leukemias are classified as lymphoid or myeloid, dependent on the type of stem cell that is affected. In addition, leukemia is classified as chronic or acute. Acute leukemia is a production of bone marrow-derived immature cells (blasts), include solid organs or peripheral blood. The FAB Cooperative Group original classification scheme proposed to divide1 ALL into three subtypes (L1 - L3). Currently, the world health organization (WHO), modify FAB classification depending on immunophenotype. Symptoms presence of anemia, splenomegaly, and thrombocytopenia, and those are naturally present at diagnosis, indicating the degree to which leukemic lymphoblasts have replaced the bone marrow and the first mark to an ALL diagnosis is typically an abnormal complete blood count result. Objective: To introduce causes of acute lymphocytic leukemia, recent classification methods, diagnosis, and symptoms and diagnosis. Conclusion: Acute lymphocytic leukemia occurs due to a defect in the bone marrow and is classified into several types. The most important classification by the World Health Organization is depending on immunophenotype. The main symptoms are the increase in white blood cells with anemia and thrombocytopenia.
URI: https://djm.uodiyala.edu.iq/index.php/djm
http://148.72.244.84:8080/xmlui/handle/xmlui/5607
ISSN: Print ISSN 2219-9764
Online ISSN 2617-8982
Appears in Collections:مجلة ديالى الطبية / Diyala Journal of Medicine

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