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Journal ArticleDOI

A clinical overview of IgG4-related systemic disease.

Arezou Khosroshahi, +1 more
- 01 Jan 2011 - 
- Vol. 23, Iss: 1, pp 57-66
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TLDR
IgG4-RSD is an underrecognized condition about which knowledge is now growing rapidly, yet there remain many unknowns with regard to its cause, pathogenesis, various clinical presentations, approach to treatment, disease monitoring, and long-term outcomes.
Citations
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Journal ArticleDOI

IgG4-related disease

TL;DR: Identification of specific antigens and T-cell clones that drive the disease will be the first steps to elucidate the pathogenesis of IgG4-related disease.
Journal ArticleDOI

Rituximab for the treatment of IgG4-related disease: lessons from 10 consecutive patients.

TL;DR: Treatment with RTX led to prompt clinical and serologic improvement in refractory IgG4-RD in all patients with active inflammation, and Serial treatments with RTX may lead to progressive declines in serum IgG 4 concentrations and better disease control.
Journal ArticleDOI

IgG4-related disease.

TL;DR: The diagnosis of IgG4-RD unifies many eponymous fibroinflammatory conditions that had previously been thought to be confined to single organs and is now being recognized with increasing frequency.
References
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Journal ArticleDOI

High serum IgG4 concentrations in patients with sclerosing pancreatitis.

TL;DR: Patients with sclerosing pancreatitis have high serum IgG4 concentrations, providing a useful means of distinguishing this disorder from other diseases of the pancreas or biliary tract.
Journal ArticleDOI

Chronic pancreatitis caused by an autoimmune abnormality : proposal of the concept of autoimmune pancreatitis

TL;DR: In this paper, the authors reported a case of chronic pancreatitis in which an autoimmune mechanism is involved in the etiology and summarized the cases of pancreatitis suspected of being caused by an auto-antibody-positive mechanism in the Japanese and English literature.
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A new clinicopathological entity of IgG4-related autoimmune disease

TL;DR: It is suggested that AIP is not simply pancreatitis but that it is a pancreatic lesion involved in IgG4-related systemic disease with extensive organ involvement, and a new clinicopathological entity is proposed.
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Diagnosis of autoimmune pancreatitis: the Mayo Clinic experience.

TL;DR: D diagnosis of autoimmune pancreatitis can be made in patients with > or =1 of these criteria: diagnostic histology, characteristic imaging on computed tomography and pancreatography with elevated serum IgG4 level, or response to steroid therapy of pancreatic/extrapancreatic manifestations of AIP.
Journal ArticleDOI

Immunoglobulin G4–Associated Cholangitis: Clinical Profile and Response to Therapy

TL;DR: IAC should be suspected in unexplained biliary strictures associated with increased serum IgG4 and unexplained pancreatic disease, especially with proximal strictures, and the role of immunomodulatory drugs for relapses needs further study.
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