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Waldenström macroglobulinemia / [E-Book]

By: Contributor(s): Series: Fast facts for healthcare professionalsPublisher: Oxford : Karger, 2022Description: 1 online resource (74 pages) : illustrations (colour)ISBN:
  • 9783318071955 (PDF ebook) :
Subject(s): Online resources: Summary: Waldenström macroglobulinemia (WM) is a rare lymphoplasmacytic lymphoma characterized by the presence of an immunoglobulin M (IgM) monoclonal protein. WM is a chronic, indolent disease, which can remain undiagnosed for years. A better understanding of the role of signaling pathways in the development of the disease and the identification of clinical and genetic markers have driven the development of targeted therapeutic strategies, improving overall survival. In this resource, the authors distill current knowledge on the pathophysiology, epidemiology and etiology of WM and discuss how the disease may present, how it is diagnosed and when treatment should be initiated. They also provide an overview of current approaches to treatment as well as ongoing and planned research directions.
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Also issued in print: 2022.

Includes bibliographical references and index.

Waldenström macroglobulinemia (WM) is a rare lymphoplasmacytic lymphoma characterized by the presence of an immunoglobulin M (IgM) monoclonal protein. WM is a chronic, indolent disease, which can remain undiagnosed for years. A better understanding of the role of signaling pathways in the development of the disease and the identification of clinical and genetic markers have driven the development of targeted therapeutic strategies, improving overall survival. In this resource, the authors distill current knowledge on the pathophysiology, epidemiology and etiology of WM and discuss how the disease may present, how it is diagnosed and when treatment should be initiated. They also provide an overview of current approaches to treatment as well as ongoing and planned research directions.

Specialized.

Description based on online resource; title from PDF title page (viewed on June 26, 2023).

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