13.4: Waldenstrom Macroglobulinemia
- Page ID
- 38845
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Features:
Commonly characterized by an IgM monoclonal gammopathy. Increased igM may also result in cryoglobulinemia. Deposits of IgM into tissues and organs can result in intestinal dysfunction, clotting, and neuropathic complications.1
Cause:1,2
Genetic mutations
Inherited associations
Following viral infections (e.g. Hepatitis C).
Age Group Affected: 60-70 years old, slightly more predominant in males.1,2
Laboratory Results for Waldenstrom Macroglobulinemia:1,2
|
CBC: WBC: Increased (But lower than CLL) |
PBS: Increased number of small lymphocytes and maybe plasmacytoid lymphocytes. |
BM: Infiltration of small lymphocytes Variable number of plasma cells and plasmacytoid lymphocytes. |
|
Immunologic Markers: CD19, CD20, CD22, CD25, CD27, CD38, CD79a |
Other Tests: Monoclonal Paraprotein IgM: Positive |
References:
1. Swerdlow SH, Campo E, Harris NL, Jaffe ES, Pileri SA, Stein H, et al. editors. WHO Classification of Tumours of Haematopoietic and Lymphoid Tissues Volume 2. 4th ed. International Agency for Research on Cancer (IARC); 2008.
2. Yun S, Johnson AC, Okolo ON, Arnold SJ, McBride A, Zhang L, et al. Waldenström Macroglobulinemia: Review of Pathogenesis and Management. Clin Lymphoma, Myeloma Leuk [Internet]. 2017 May 7 [cited 2018 Jun 27];17(5):252–62. Available from: http://www.ncbi.nlm.nih.gov/pmc/articles/PMC5413391/