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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Detalhes bibliográficos
Main Authors: Bignon, Y J, Janin-Mercier, A, Dubost, J J, Ristori, J M, Fonck, Y, Alphonse, J C, Sauvezie, B J
Formato: Artigo
Idioma:Inglês
Publicado em: 1986
Assuntos:
Research Article
Acesso em linha:https://ncbi.nlm.nih.gov/pmc/articles/PMC1001926/
https://ncbi.nlm.nih.gov/pubmed/3729577
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