Rheumatoid arthritis in a patient with primary hypogammaglobulinaemia

Br J Rheumatol. 1993 Jul;32(7):636-9. doi: 10.1093/rheumatology/32.7.636.

Abstract

A 44-year-old woman with primary hypogammaglobulinaemia developed classical RA and inflammatory bowel disease. She represents an example of rheumatoid disease developing in the absence of endogenous antibodies and raises interesting questions regarding the pathophysiology of the disease.

Publication types

  • Case Reports

MeSH terms

  • Adult
  • Agammaglobulinemia / complications*
  • Agammaglobulinemia / physiopathology
  • Arthritis, Rheumatoid / etiology*
  • Arthritis, Rheumatoid / physiopathology
  • Female
  • Humans
  • Inflammatory Bowel Diseases / etiology
  • Inflammatory Bowel Diseases / physiopathology