Journal of Hematology

ISSN 1927-1212 print
ISSN 1927-1220 online
Frequency: Quarterly
Journal Access: Open Access
Journal scope: Journal of Hematology is an international, peer-reviewed journal, publishing original contributions describing basic research and clinical investigation of hematology and transfusion medicine, on the cellular, molecular, prevention, diagnosis, therapy and prognosis aspects.
Indexed and covered by: Chemical Abstract (CA);
Worldcat; Google; Google Scholar; JournalTOCs; PubMed: selected citations only.
Journal archiving and digital preservation: Portico


Highlights

  • Beta-Globin Haplotypes and Alpha-Thalassemia 3.7 kb Deletion in Sickle Cell Disease Patients From the Occidental Brazilian Amazon

    Sickle cell disease (SCD) includes a group of inherited red blood cell disorders. SCD patients vary widely from person to person. We describe βS and βC haplotypes and α-thalassemia 3.7 kb genotypes from SCD patients Fundacao Hospitalar de Hematologia e Hemoterapia do Amazonas, Manaus, AM.

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  • Concurrent Presentation of High-Grade Lymphoma and Metastatic Pancreatic Neuroendocrine Tumor 14 Years After Renal Transplant

    The development of malignancy, especially lymphoma, is common after solid organ transplant. However, concurrent malignancies are rare and result in a diagnostic and treatment dilemma, particularly in the post-transplant setting.

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  • Arterial and Venous Estimation of Hemoglobin: A Correlational Study

    The objective of this study was to identify the correlation between arterial blood gas (ABG) hemoglobin and venous hemoglobin in acutely ill patients.

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  • A Rare Variant of Aggressive T-Cell Large Granular Lymphocyte Leukemia Associated With Hepatic Fibrosis and Trisomy 8

    Aggressive T-cell large granular lymphocytic leukemia (T-LGL) is a rare entity with a poor prognosis, the main clinical findings being splenomegaly, lymphadenopathy, thrombocytopenia and a CD3+/CD56+ phenotype.

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  • Mobile Thrombus in the Ascending Aorta Associated With Acute Myocardial Infarction

    The presence of thrombus in the ascending aorta is uncommon but it has been implicated in systemic thromboembolism.

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Viewpoints

 

 

Featured Article

 

Potential Benefits of Metformin Use in Sickle Cell Anemia
Sickle cell anemia (SCA) is one of the most important genetic disorders known to mankind. Even with the impressive advances in medical science, effective treatment and cure remain challenging. Currently available treatments including hydroxyurea, which is the only FDA approved drug for SCA, and hemopoietic stem cell transplantation all have significant limitations, so the search for new therapeutic options continues. Read the Full Text

Warm Autoimmune Hemolytic Anemia: Clinical Profile and Management
Autoimmune hemolytic anemia (AIHA) is a rare autoimmune disease in which autoantibodies target red blood cells leading to marked decrease in their lifespan. The classification of AIHA is based on the immunochemical properties of the RBC autoantibody. Warm antibody AIHA (wAIHA) accounts for 75-80% of all adult AIHA cases. The treatment of wAIHA is mainly corticosteroids. Read the Full Text


Image of the Issue

Ebstein-Barr Virus-Negative Clonal Plasma Cell Proliferations Associated With Systemic Involvement of Primary Cutaneous T-Cell Lymphoma
We describe a 66-year-old man with a long-standing history of squamous cell carcinoma of the head and neck region who developed nodular-sclerosing subtype of classical Hodgkin lymphoma and primary cutaneous CD8-positive, cytotoxic variant of mycosis fungoides over a 1-year period of time. Within a few months of his diagnosis of primary cutaneous T-cell lymphoma, he developed systemic involvement of T-cell lymphoma in an axillary lymph node, bone marrow and lung. Full Text

Current Issue

Past Issues


Vol. 6, No. 4, Oct 2017

Table of Contents

Original Article

The DAU Allele and Anti-D Alloimmunization Present With High Frequency in Brazilian Sickle Cell Disease Patients Abstract HTML PDF
Jose Pereira de Moura Neto, Bruno Antonio Veloso Cerqueira, Wendell Vilas Boas Santos, Isa Menezes Lyra, Marilda Souza Goncalves 73-80
doi: https://doi.org/10.14740/jh316w
Regulatory and memory B lymphocytes in children with newly diagnosed immune thrombocytopenia Abstract HTML PDF
Asmaa M. Zahran, Sanaa Shaker Aly, Ahmed Elabd, Ismail Lotfy Mohamad, Khalid I. Elsayh 81-86
doi: https://doi.org/10.14740/jh336w

Case Report

Methemoglobinemia: A Rare Entity Caused by Commonly Used Topical Anesthetic Agents, a Case Report Abstract HTML PDF
Prashanth Rawla, Jeffrey Pradeep Raj 87-89
doi: https://doi.org/10.14740/jh325w
Infiltrative Rash Secondary to Leukemic-Phase Diffuse Large B-Cell Lymphoma With t(14;18), CDKN2A and MLL Deletion Abstract HTML PDF
Iris Y. Sheng, Diana O. Treaba, Kenneth D. Bishop 90-95
doi: https://doi.org/10.14740/jh327w
A Case of Therapy-Related Acute Myeloid Leukemia in a Patient With Heterozygous Mutations in the Ataxia Telangiectasia Mutated Gene Abstract HTML PDF
Andrew Shieh, Ali A. Mohamed 96-100
doi: https://doi.org/10.14740/jh330w
Revisiting Howell-Jolly Body-Like Cytoplasmic Inclusions in Neutrophils: A Report of Two Cases and Confirmation of Nuclear Origin Abstract HTML PDF
Reeba Omman, Christina Kwong, Daniel Shepherd, Jo A. Molnar, Milind M. Velankar, Kamran M. Mirza 101-104
doi: https://doi.org/10.14740/jh334w
Two Novel Monoallelic Calreticulin Mutations in a Patient With Essential Thrombocythemia Abstract HTML PDF
Eniko Kamory, Thomas Schmidt, Cedric Broquere, Hartmut Peters, Berthold Hocher 105-108
doi: https://doi.org/10.14740/jh335w
 
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Journal of Hematology, quarterly, ISSN 1927-1212 (print), 1927-1220 (online), published by Elmer Press Inc.            
The content of this site is intended for health care professionals.
This is an open-access journal distributed under the terms of the Creative Commons Attribution-NonCommercial 4.0 International License, which permits unrestricted
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