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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Detaylı Bibliyografya
Asıl Yazarlar: Bignon, Y J, Janin-Mercier, A, Dubost, J J, Ristori, J M, Fonck, Y, Alphonse, J C, Sauvezie, B J
Materyal Türü: Artigo
Dil:Inglês
Baskı/Yayın Bilgisi: 1986
Konular:
Research Article
Online Erişim:https://ncbi.nlm.nih.gov/pmc/articles/PMC1001926/
https://ncbi.nlm.nih.gov/pubmed/3729577
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