Angioimmunoblastic lymphadenopathy with dysproteinaemia (AILD) and sicca syndrome.

@article{Bignon1986AngioimmunoblasticLW,
  title={Angioimmunoblastic lymphadenopathy with dysproteinaemia (AILD) and sicca syndrome.},
  author={Yves Jean Bignon and Anne Janin-Mercier and Jean-Jacques Dubost and Jean Michel Ristori and Yvette Fonck and J. C. Alphonse and Bernard Sauvezie},
  journal={Annals of the rheumatic diseases},
  year={1986},
  volume={45 6},
  pages={
          519-22
        }
}
We report a case of AILD and sicca syndrome. The patient had presented with renal insufficiency, lymphadenopathy, hepatosplenomegaly, polyclonal hypergammaglobulinaemia, dryness of the eyes and mouth. Lip biopsy specimens showed an unusual cellular infiltrate similar to his kidney lesions. Data from the eight previously reported cases support the hypothesis that the association is a distinct pathological entity differing from pseudolymphoma and malignant lymphoma, which occur in the course of… CONTINUE READING

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