IgG4-Related Orbitopathy

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منابع مشابه

A Case of IgG4-related Orbitopathy

IgG4-related disease is an immune-mediated disorder affecting almost all major organs of the body. A 62-year-old male, who was diagnosed with an orbital tumor and a nasal-orbital communicating tumor of the left eye, underwent endoscopic endonasal removal of the orbital tumor and fenestration of the ethmoid sinus. The tumor originated in the orbital tissue and showed pathological changes associa...

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Exophthalmos in a young woman with no graves’ disease – a case report of IgG4-related orbitopathy

BACKGROUND Immunoglobulin G4-related disease (IgG4-rd) is characterized by lymphoplasmacytic infiltration and tissue fibrosis. Orbital manifestations of IgG4-rd may include unilateral or bilateral proptosis, cicatricial extraocular muscle myopathy, orbital inflammation and pain which may mimic ophthalmic Graves' disease. CASE PRESENTATION A 25-year-old woman has been referred to the endocrino...

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IgG4-related prostatitis progressed from localized IgG4-related lymphadenopathy.

Immunoglobulin G4-related disease (IgG4-RD) is a recently described inflammatory disease involving multiple organs. Prostate involvement with IgG4-RD is very rare. In this report, we describe a case of IgG4-related prostatitis progressed from localized IgG4-related lymphadenopathy. This patient was present with urine retention symptoms. MRI and CT examination revealed the prostatic enlargement ...

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IgG4-Related Perineural Disease

Aims. To elucidate characteristics of IgG4-related disease involving the peripheral nervous system. Methods. Retrospective review of 106 patients with IgG4-related disease identified 21 peripheral nerve lesions in 7 patients. Clinicopathological and radiological features were examined. Results. Peripheral nerve lesions were commonly identified in orbital or paravertebral area, involving orbital...

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IgG4-related sclerosing disease.

Based on histological and immunohistochemical examination of various organs of patients with autoimmune pancreatitis (AIP), a novel clinicopathological entity of IgG4-related sclerosing disease has been proposed. This is a systemic disease that is characterized by extensive IgG4-positive plasma cells and T-lymphocyte infiltration of various organs. Clinical manifestations are apparent in the pa...

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ژورنال

عنوان ژورنال: Middle East African Journal of Ophthalmology

سال: 2015

ISSN: 0974-9233

DOI: 10.4103/0974-9233.167816