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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Bibliographic Details
Main Authors:	Bignon, Y J, Janin-Mercier, A, Dubost, J J, Ristori, J M, Fonck, Y, Alphonse, J C, Sauvezie, B J
Format:	Artigo
Language:	Inglês
Published:	1986
Subjects:	Research Article
Online Access:	https://ncbi.nlm.nih.gov/pmc/articles/PMC1001926/ https://ncbi.nlm.nih.gov/pubmed/3729577
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Angioimmunoblastic lymphadenopathy with dysproteinaemia (AILD) and sicca syndrome.

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