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==Overview==
==Overview==

Revision as of 01:54, 31 October 2018

Waldenström's macroglobulinemia Microchapters

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Roukoz A. Karam, M.D.[2] Mirdula Sharma, MBBS [3]

Overview

Laboratory findings consistent with the diagnosis of Waldenström's macroglobulinemia include any cytopenia, elevated LDH, and elevated Beta-2 microglobulin.

Laboratory Findings

Laboratory findings consistent with the diagnosis of [disease name] include:

  • Complete blood count:
    • Anemia
      • Seen in 40% of newly diagnosed patients and in 80% of symptomatic patients with Waldenström's macroglobulinemia
      • Multifactorial causes including: decreased RBC synthesis due to bone marrow infiltration, iron deficiency due to gastrointestinal bleeding, chronic inflammation.
    • Thrombocytopenia
      • Due to bone marrow infiltration
    • Neutropenia
      • Due to bone marrow infiltration
    • Lymphocytosis
    • Monocytosis
  • Peripheral smear:
    • Plasmacytoid lymphocytes
    • Normocytic normochromic red blood cells
    • Rouleaux formation
  • Serum and urine protein electrophoresis:
    • Screening test for Waldenström macroglobulinemia [1]
    • Detection of M spike
  • Serum and urine immunofixation
    • Confirmatory test for waldenström's macroglobulinemia[1]
    • Determines the IgM type of immunoglobulin
  • Chemistry Lab tests
  • Plasma viscosity
    • Plasma viscosity should be measured in patients presenting with hyperviscosity syndrome whenever the monoclonal IgM protein spike is >4 g/dL.
    • The normal plasma viscosity is 1.8 centipoise.
    • Patient presents with hyperviscosity symptoms with viscosity >4 centipoise.

References

  1. 1.0 1.1 Waldenström macroglobulinaemia. American Cancer Society (2015) http://www.cancer.org/cancer/waldenstrommacroglobulinemia/detailedguide/waldenstrom-macroglobulinemia-diagnosis Accessed on November 15th, 2015

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