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Revista Cubana de Reumatología

ISSN 1817-5996 (Electronic)
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2016, Number 1

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Rev Cub de Reu 2016; 18 (1)

Rheumatoid arthritis and thrombocytopenic purpura associated with common variable immunodeficiency

Saldarriaga RLM, Delgado QLA, Ríos GBBE
Full text How to cite this article

Language: Spanish
References: 11
Page: 62-65
PDF size: 68.26 Kb.


Key words:

rheumatoid arthritis, thrombocytopenic purpura, common variable immunodeficiency, autoimmune disease.

ABSTRACT

Common variable immunodeficiency is a disorder characterized by low levels of serum immunoglobulins associated with increased susceptibility to infections. In some patients there is a reduction in both IgG and IgA, in some others, the reduction is present in three main types of immunoglobulins (IgG, IgA and IgM). Frequent and unusual infections can occur in childhood, but in most patients the diagnosis is delayed. Diseases like rheumatoid arthritis and thrombocytopenic purpura are immune system disorders that can be associated with common variable immunodeficiency.


REFERENCES

  1. Abbott JK, Gelfand EW. Common Variable Immunodeficiency: Diagnosis, Management, and Treatment. Immunol Allergy Clin North Am. 2015;35(4):637-58.

  2. Hammarström L, Vorechovsky I, Webster D. Selective IgA deficiency (SIgAD) and common variable immunodeficiency (CVID). Clin Exp Immunol. 2000;120(2):225-31.

  3. Saifi M, Wysocki CA. Autoimmune Disease in Primary Immunodeficiency: At the Crossroads of Anti-Infective Immunity and Self-Tolerance. Immunol Allergy Clin North Am. 2015;35(4):731-52.

  4. Conley ME, Notarangelo LD, Etzioni A. Diagnostic criteria for primary immunodeficiencies. Representing PAGID (Pan-American Group for Immunodeficiency) and ESID (European Society for Immunodeficiencies). Clin Immunol. 1999; 93(3):190-7.

  5. Bonilla FA, Bernstein I, Khan D, Ballas ZK, Chimen J, Frank MM, et al. Practice parameter for diagnosis and management of primary immunodeficiency. Ann Allergy Asthma Immunol. 2005; 94:S1-64.

  6. Gathmann B, Grimbacher B, BeautéJ, Dudoit Y, Mahlaoui N, Fischer A, et al. The European internet-based patient and research database for primary immunodeficiencies: results 2006-2008. Clin Exp Immunol. 2009;157(Suppl 1):3-11.

  7. Ameratunga R, Brewerton M, Slade C, Jordan A, Gillis D, Steele R, Koopmans W, Woon ST. Comparison of diagnostic criteria for common variable immunodeficiency disorder. Front Immunol. 2014;15(5):415

  8. Seidel MG. Autoimmune and other cytopenias in primary immunodeficiencies: pathomechanisms, novel differential diagnoses, and treatment. Blood. 2014;124(15):2337-44.

  9. Cunningham-Rundles C, Bodian C. Common variable immunodeficiency: Clinical and immunological features of 248 patients. Clin Immunol. 1999; 92:34-48.

  10. Saldarriaga Rivera LM, Quiroz LAD, Bica BERG. Enfermedad Indiferenciada de Tejido Conectivo asociada a Deficiencia de IgG2 e IgG4. Rev Cubana de Reumatol. 2014; 16(01):47-51.

  11. Oksenhendler E, Gérard L, Fieschi C, Malphettes M, Mouillot G, Jaussaud R, et al. Infections in 252 patients with common variable immunodeficiency. Clin Infect Dis. 2008;46(10):1547-54.




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Rev Cub de Reu. 2016;18