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Multiple myeloma and immunosecretory disorders: an update
Saad P Shaheen1, Sameer S Talwalkar, L Jeffrey Medeiros
1Department of Pathology, Veterans Affair Medical Center, Louisville, KY, USA.
Advances in Anatomic Pathology
|June 27, 2008
Summary
Immunosecretory disorders, including multiple myeloma, stem from abnormal B cell proliferation. Modern classification integrates clinical, morphologic, and biologic data for accurate diagnosis and understanding of disease progression.
Area of Science:
- Hematology
- Oncology
- Immunology
Background:
- Immunosecretory disorders involve abnormal immunoglobulin (Ig)-synthesizing B cell proliferation.
- These conditions include multiple myeloma (MM), Waldenstrom macroglobulinemia, and monoclonal Ig deposition diseases.
- Diagnosis has been challenging due to diverse classifications, often relying on morphology.
Purpose of the Study:
- To review the modern classification of immunosecretory disorders.
- To highlight the integration of various parameters for diagnosis and understanding disease progression.
- To address the evolution of classification schemes, including WHO and International Myeloma Group criteria.
Main Methods:
- Review of existing literature and classification systems.
- Integration of clinical, morphologic, laboratory, radiographic, and biologic data.
- Analysis of diagnostic criteria and definitions for immunosecretory disorders.
Main Results:
- Immunosecretory disorders are characterized by monoclonal protein (M-protein) production.
- Previous classifications, primarily morphologic, posed diagnostic challenges.
- The 2003 International Myeloma Group definition clarified MM by linking it to organ damage.
Conclusions:
- Modern classification requires integrating clinical, morphologic, laboratory, radiographic, and biologic parameters.
- Accurate classification is crucial for understanding disease progression and patient outcomes.
- The evolution of classification reflects a move towards a more comprehensive diagnostic approach.
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