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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Main Authors: Bignon, Y J, Janin-Mercier, A, Dubost, J J, Ristori, J M, Fonck, Y, Alphonse, J C, Sauvezie, B J
Format: Artigo
Jezik:Inglês
Izdano: 1986
Teme:
Research Article
Online dostop:https://ncbi.nlm.nih.gov/pmc/articles/PMC1001926/
https://ncbi.nlm.nih.gov/pubmed/3729577
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