IgG4-positive multi-organ lymphoproliferative syndrome manifesting as chronic symmetrical sclerosing dacryo-sialadenitis with subsequent secondary portal hypertension and remarkable IgG4-linked IL-4 elevation-Reference-Cited by-同舟云学术

IgG4-positive multi-organ lymphoproliferative syndrome manifesting as chronic symmetrical sclerosing dacryo-sialadenitis with subsequent secondary portal hypertension and remarkable IgG4-linked IL-4 elevation

Published:2010-05-05 Issue:9 Volume:49 Page:1789-1791
ISSN:1462-0324
Container-title:Rheumatology
language:en
Short-container-title:Rheumatology

Author:

Suzuki K.,Tamaru J.-i.,Okuyama A.,Kameda H.,Amano K.,Nagasawa H.,Nishi E.,Yoshimoto K.,Setoyama Y.,Kaneko K.,Osada H.,Honda N.,Sasaki Y.,Itoyama S.,Tsuzaka K.,Takeuchi T.

Publisher

Oxford University Press (OUP)

Subject

Pharmacology (medical),Rheumatology

Link

http://academic.oup.com/rheumatology/article-pdf/49/9/1789/5050520/keq113.pdf

Reference10 articles.

1. Clinical and pathological differences between Mikulicz's disease and Sjögren's syndrome

2. Proposal for a new clinical entity, IgG4-positive multiorgan lymphoproliferative syndrome: analysis of 64 cases of IgG4-related disorders

3. Hyper-IgG4 disease: report and characterisation of a new disease

5. A case of Mikulicz’s disease complicated with severe interstitial nephritis associated with IgG4

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