Angioimmunoblastic lymphadenopathy with dysproteinaemia (AILD) and sicca syndrome.

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...

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Bibliografiske detaljer
Main Authors: Bignon, Y J, Janin-Mercier, A, Dubost, J J, Ristori, J M, Fonck, Y, Alphonse, J C, Sauvezie, B J
Format: Artigo
Sprog:Inglês
Udgivet: 1986
Fag:
Research Article
Online adgang:https://ncbi.nlm.nih.gov/pmc/articles/PMC1001926/
https://ncbi.nlm.nih.gov/pubmed/3729577
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