Overview
Hematological malignancies are cancers that arise from cells of the blood, bone marrow, and lymphatic system, originating in the hematopoietic and lymphoid lineages rather than forming solid organ tumors. They are broadly classified into leukemias, which involve clonal proliferation of myeloid or lymphoid precursors in the marrow and blood; lymphomas, which develop in lymph nodes and lymphoid tissues and include Hodgkin and non-Hodgkin subtypes; and plasma cell disorders such as multiple myeloma and Waldenström's macroglobulinemia, marked by malignant antibody-producing cells. These diseases arise from acquired genetic and epigenetic alterations that disrupt normal differentiation, proliferation, and apoptosis, with leukemogenesis often driven by mutations, chromosomal translocations, and dysregulated signaling in hematopoietic stem and progenitor cells. Surface markers and molecular profiles are central to classification and diagnosis, and aberrant expression of receptors and signaling proteins can distinguish malignant clones. Hematological malignancies may also perturb hemostasis, producing acquired coagulation abnormalities, and can present with paraneoplastic syndromes affecting other organ systems. Diagnosis integrates morphology, immunophenotyping, cytogenetics, and molecular testing, while management spans chemotherapy, targeted agents, immunotherapy, and stem cell transplantation. Research in this area examines the molecular markers, microenvironmental interactions, and clonal evolution that govern disease behavior, prognosis, and the response to therapy.
Research published in this journal
7 peer-reviewed articles, ranked by relevance. Each links to its DOI.
Cholesterol-Conjugated siRNA Accumulates in the Different Hematopoietic and Lymphoid Cells.
Acquired Abnormalities of Plasma Von Willebrand Factor Related Parameters and ADAMTS13 Autoantibodies in Aggressive Haematological Malignancies.
Role of Tie2, CD14, Angiopoietin as Angiogenetic Markers in Hepatocellular Carcinoma Complicating Hepatitis C Virus Infection
Deficiency of Adenosine Deaminase Type 2 (ADA2) DADA2 Masquerade as Lupus
Syndrome of inappropriate antidiuretic hormone secretion in a patient with a Nodular Lymphocyte-Predominant Hodgkin Lymphoma. A case report and review of literature
The Daughter of Time: Late Development of Waldenstrom’s Macroglobulinemiain a Patient with Immunotactoid Glomerulopathy.
How this research is being cited
The 7 articles above have been cited 21 times in the scholarly literature. Citation data via OpenAlex and Crossref, updated Jun 2026.
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2026 · Biomolecules
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Dina Ashraf Abdelhady et al. · 2025 · European Journal of Medical Research
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2025 · European journal of medical research
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2024 · Expert Opinion on Drug Safety
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2024 · Expert Opinion on Drug Safety
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2023 · Expert Opinion on Drug Discovery
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2022 · Expert Opinion on Drug Discovery
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Wolfgang Neukirchen et al. · 2022 · Case Reports in Nephrology and Dialysis
A sample of recent works citing this journal's research on Hematological-malignancies, linking to each citing work.