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A Comprehensive Exploration of Waldenström Macroglobulinemia (WM)
Waldenström macroglobulinemia (WM), a rare lymphoplasmacytic lymphoma, is characterized by the presence of an immunoglobulin M (IgM) monoclonal protein. This chronic, indolent disease often remains undetected for prolonged periods.
Recent advancements have illuminated the crucial role of signaling pathways in WM development and facilitated the identification of clinical and genetic markers guiding targeted therapeutic strategies. Consequently, overall survival rates have witnessed notable improvements.
This comprehensive resource meticulously distills current knowledge regarding WM’s pathophysiology, epidemiology, and etiology. It elucidates the disease’s diverse clinical presentations, diagnostic methodologies, and the appropriate timing for treatment initiation. Furthermore, it provides a panoramic view of current treatment approaches and ongoing or projected research endeavors.
The wealth of information presented within these pages caters to professionals dedicated to the field of WM research and clinical management. Specialist nurses and trainees in hematology, oncology, gerontology, pathology, and neurology will find this resource invaluable in their pursuit of expanding their understanding and advancing their practice.
Table of Contents
- Epidemiology, Etiology, and Overview:
- Prevalence, risk factors, and molecular pathogenesis
- Clinical manifestations and disease variants
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Differential diagnosis and initial patient assessment
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Diagnostic Work-Up and Prognosis:
- Laboratory tests and imaging modalities
- Histological and molecular diagnostics
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Prognostic indicators and risk stratification
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Treatment:
- Non-chemotherapy approaches
- Chemotherapy and immunotherapy
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Emerging therapies and hematopoietic stem cell transplantation
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Research Directions:
- Novel therapeutic targets and drug discovery
- Biomarkers for diagnosis, prognosis, and treatment selection
- Patient-centered outcomes and survivorship
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