Waldenström's macroglobulinemia laboratory findings: Difference between revisions

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**Normocytic normochromic red blood cells
**Normocytic normochromic red blood cells
**[[Rouleaux]] formation
**[[Rouleaux]] formation
* '''Chemistry Lab tests:'''
* '''Chemistry Lab tests:'''<ref name="pmid19520758">{{cite journal| author=Katzmann JA, Kyle RA, Benson J, Larson DR, Snyder MR, Lust JA et al.| title=Screening panels for detection of monoclonal gammopathies. | journal=Clin Chem | year= 2009 | volume= 55 | issue= 8 | pages= 1517-22 | pmid=19520758 | doi=10.1373/clinchem.2009.126664 | pmc=3773468 | url=https://www.ncbi.nlm.nih.gov/entrez/eutils/elink.fcgi?dbfrom=pubmed&tool=sumsearch.org/cite&retmode=ref&cmd=prlinks&id=19520758  }} </ref>
**Elevated [[lactate dehydrogenase]] (LDH)
**Elevated [[lactate dehydrogenase]] (LDH)
***Level indicates the extent of the disease
***Level indicates the extent of the disease
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*** Possibly due to interaction between platelet surface glycoproteins and IgM paraprotein
*** Possibly due to interaction between platelet surface glycoproteins and IgM paraprotein
** Abnormalities in prothrombin time, activated partial thromboplastin time, thrombin time, and fibrinogen
** Abnormalities in prothrombin time, activated partial thromboplastin time, thrombin time, and fibrinogen
* '''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==
==References==

Revision as of 02:15, 31 October 2018

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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 Waldenström macroglobulinemia include:[1]

  • 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
  • Chemistry Lab tests:[2]
  • Platelet function test and blood coagulation studies:
    • Prolonged bleeding time[3]
      • Possibly due to interaction between platelet surface glycoproteins and IgM paraprotein
    • Abnormalities in prothrombin time, activated partial thromboplastin time, thrombin time, and fibrinogen

References

  1. García-Sanz R, Montoto S, Torrequebrada A, de Coca AG, Petit J, Sureda A; et al. (2001). "Waldenström macroglobulinaemia: presenting features and outcome in a series with 217 cases". Br J Haematol. 115 (3): 575–82. PMID 11736938.
  2. Katzmann JA, Kyle RA, Benson J, Larson DR, Snyder MR, Lust JA; et al. (2009). "Screening panels for detection of monoclonal gammopathies". Clin Chem. 55 (8): 1517–22. doi:10.1373/clinchem.2009.126664. PMC 3773468. PMID 19520758.
  3. Penny R, Castaldi PA, Whitsed HM (1971). "Inflammation and haemostasis in paraproteinaemias". Br J Haematol. 20 (1): 35–44. PMID 4924493.

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