How Is Waldenström Macroglobulinemia Diagnosed?
Diagnosing Waldenström macroglobulinemia (WM) involves a series of evaluations, including a physical exam, a review of your medical history, and specialized blood and bone marrow tests.
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Expert Advice for Newly Diagnosed Waldenström Macroglobulinemia (WM) Patients
Waldenström Macroglobulinemia Staging
Unlike many other lymphomas, Waldenström macroglobulinemia does not follow a traditional staging system. Instead, healthcare providers assess disease progression based on symptoms, IgM levels, and bone marrow involvement.
Essential Testing
A definitive diagnosis of WM requires several key tests, including:
- Blood Tests: determine the types and amounts of antibodies in your blood
- Bone Marrow Aspiration and Biopsy: Confirms the presence of abnormal lymphoplasmacytic cells
- Genetic Testing: Identifies MYD88 and CXCR4 mutations, which can influence treatment decisions
- Imaging Tests: Such as a CT or PET scan to determine if the cancer has spread beyond the bone marrow
Waldenström Macroglobulinemia Diagnosis & Testing Programs
Provides actionable advice and downloadable materials to help you communicate clearly and effectively with your WM healthcare team.
Topics:
- Understanding Waldenström Macroglobulinemia
- Waldenström Macroglobulinemia Treatment Approaches
- Tips for Waldenström Macroglobulinemia Patient Self-Advocacy
- Planning Your Waldenström Macroglobulinemia Doctor’s Office Visit
- Pro-Active Waldenström Macroglobulinemia Patient Resources
