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Monoclonal gammopathy

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Excess myeloma protein or monoclonal gamma globulin in the blood Medical condition
Monoclonal gammopathy
Other namesparaproteinemia
Serum protein electrophoresis shows gamma spike, or peak
SpecialtyOncology Edit this on Wikidata

Monoclonal gammopathy, also known as paraproteinemia, is the presence of excessive amounts of myeloma protein or monoclonal gamma globulin in the blood. It is usually due to an underlying immunoproliferative disorder or hematologic neoplasms, especially multiple myeloma. It is sometimes considered equivalent to plasma cell dyscrasia. The most common form of the disease is monoclonal gammopathy of undetermined significance.

Causes

Main article: Plasma cell dyscrasia

Causes of paraproteinemia include the following:

Diagnosis

These are characterized by the presence of any abnormal protein that is involved in the immune system, which are most often immunoglobulins and are associated with the clonal proliferation of lymphocytes.

When a paraproteinemia is present in the blood, there will be a narrow band, or spike, in the serum protein electrophoresis because there will be an excess of production of one protein.

There are two large classes of blood proteins: albumin and globulin. They are generally equal in proportion, but albumin is much smaller than globulin, and slightly negatively charged, which leads to an accumulation at the end of the electrophoretic gel. The globulins separate out into three regions on the electrophoretic gel, which are the α band, the β band, and the γ band.

Types

Paraproteinemias may be categorized according to the type of monoclonal protein found in blood:

The three types of paraproteins may occur alone or in combination in a given individual. Note that while most heavy chains or whole immunoglobulins remain within blood vessels, light chains frequently escape and are excreted by the kidneys into urine, where they take the name of Bence Jones protein.

It is also possible for paraproteins (usually whole immunoglobulins) to form polymers by aggregating with each other; this takes the name of macroglobulinemia and may lead to further complications. For example, certain macroglobulins tend to precipitate within blood vessel with cold, a phenomenon known as cryoglobulinemia. Others may make blood too viscous to flow smoothly (usually with IgM pentamer macroglobulins), a phenomenon known as Waldenström macroglobulinemia.

The most common type of paraproteinemia is monoclonal gammopathy of undetermined significance (MGUS). Another form, monoclonal gammopathy of renal significance (MGRS) results in kidney damage and chronic kidney disease due to the effects of monoclonal immunoglobulins.

References

  1. Health Communication Network. Immunoproliferative disorders- Topic Tree. http://www.use.hcn.com.au/subject.%60Immunoproliferative%20Disorders%60/home.html Archived 2007-09-28 at the Wayback Machine. Accessed March 2007.
  2. Ma ES, Lee ET (2007). "A case of IgM paraproteinemia in which serum free light chain values were within reference intervals". Clin. Chem. 53 (2): 362–3. doi:10.1373/clinchem.2006.080317. PMID 17259251.
  3. ^ Martínez-Gómez MA, Carril-Avilés MM, Sagrado S, Villanueva-Camañas RM, Medina-Hernández MJ (2007). "Characterization of antihistamine-human serum protein interactions by capillary electrophoresis". J Chromatogr A. 1147 (2): 261–9. doi:10.1016/j.chroma.2007.02.054. PMID 17339039.
  4. Abbas, A.K and Lichtman, A.H. Cellular and Molecular Immunology. Fifth Edition. Elsevier Saunders. Philadelphia. 2005
  5. Leung, Nelson; Bridoux, Frank; Nasr, Samih H. (19 May 2021). "Monoclonal Gammopathy of Renal Significance". New England Journal of Medicine. 384 (20): 1931–1941. doi:10.1056/NEJMra1810907. PMID 34010532. S2CID 234791002.

External links

ClassificationD
Immunoproliferative immunoglobulin disorders
PCDs/PP
Other hypergammaglobulinemia
Leukaemias, lymphomas and related disease
B cell
(lymphoma,
leukemia)
(most CD19
By
development/
marker
TdT+
  • ALL (Precursor B acute lymphoblastic leukemia/lymphoma)
  • CD5+
    CD22+
    CD79a+
    RS (CD15+, CD30+)
    PCDs/PP
    (CD38+/CD138+)
    By infection
    Cutaneous
    T/NK
    T cell
    (lymphoma,
    leukemia)
    (most CD3
    By
    development/
    marker
  • TdT+: ALL (Precursor T acute lymphoblastic leukemia/lymphoma)
  • Cutaneous
    MF+variants

    aggressive: Sézary disease

    Non-MF
    Other
    peripheral
    By infection
    NK cell/
    (most CD56)
    T or NK
    Lymphoid+
    myeloid
    Lymphocytosis
    Cutaneous lymphoid hyperplasia
    General
    Category: