منابع مشابه
A Case of Type 1 Autoimmune Pancreatitis (AIP), a Form of IgG4-Related Disease (IgG4-RD)
BACKGROUND Type 1 autoimmune pancreatitis (AIP), also known as lymphoplasmacytic sclerosing pancreatitis (LPSP), is a rare cause of chronic pancreatitis, characterized by a fibro-inflammatory process. However, patients with AIP may have a good response to corticosteroid therapy. We describe a Tunisian patient with AIP that was confirmed to be an IgG4-related disease (IgG4-RD). CASE REPORT We de...
متن کاملویژگی ها IgG4 و بیماری های مرتبط با IgG4
Abstract Background: In the serum of healthy people, IgG4 has lowest concentration among the different sub-classes of IgG. Elevation of serum IgG4 in response to chronic antigenic stimulation and inflammation has been reported. Inflammation, histopathologic lesions and systemic organ involvement have been reported in the IgG4-related disease (IgG4-RD). In this article we review IgG4 unique f...
متن کاملOn generalized AIP-rings
In this paper, we introduce the concept of the generalized AIP-rings as a generalization of the generalized quasiBaer rings and generalized p.p.-rings. We show that the class of the generalized AIP-rings is closed under direct products and Morita invariance. We also characterize the 2-by-2 formal upper triangular matrix rings of this new class of rings. Finally, we provide several examples to s...
متن کاملOrgan Correlation in IgG4-Related Diseases
IgG4-related disease (IgG4-RD) is a potentially multiorgan disorder. In this study, clinical and serological features from 132 IgG4-RD patients were compared about organ correlations. Underlying pathologies comprised autoimmune pancreatitis (AIP) in 85 cases, IgG4-related sclerosing cholangitis (IgG4-SC) in 12, IgG4-related sialadenitis (IgG4-SIA) in 56, IgG4-related dacryoadenitis (IgG4-DAC) i...
متن کاملSLE and APS
Childhood-onset systemic lupus erythematosus (cSLE) represents 15-20% of all SLE cases and is in general associated with a more aggressive disease course and more rapid damage accrual than adult-onset SLE. Disease expression varies according to ethnicity, with more severe disease course in non-Caucasian ethnic groups. The majority of patients with cSLE develop damage within 5-10 years of diseas...
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ژورنال
عنوان ژورنال: Hematology & Transfusion International Journal
سال: 2017
ISSN: 2469-2778
DOI: 10.15406/htij.2017.05.00106