Neurological Manifestations of IgG4-Related Disease

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Neurological Manifestations of IgG4-Related Disease

OPINION STATEMENT IgG4-related disease (IgG4-RD) is a multisystem inflammatory disorder. Early recognition of IgG4-RD is important to avoid permanent organ dysfunction and disability. Neurological involvement by IgG4-RD is relatively uncommon, but well recognised-hypertrophic pachymeningitis and hypophysitis are the most frequent manifestations. Although the nervous system may be involved in is...

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Renal manifestations of IgG4-related systemic disease

While autoimmune pancreatitis (AIP) has been recognized since the first description by Sarles et al in 1961, its involvement of other organs has been recognized more recently. Now, some form of IgG4-related systemic disease (IgG4-RSD) has been described in nearly every organ system, including the liver, gallbladder, other gastrointestinal sites, kidney, salivary and lacrimal glands, orbit, brea...

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Intrathoracic Manifestations of IgG4-Related Disease

Intrathoracic involvement with IgG4-related disease (IgG4-RD) is frequently overlooked in IgG4-related disease patients. In this article we review the intrathoracic findings of IgG4-RD which are variable and protean. IgG4-related disease has been reported to affect the lung parenchyma, pleura, mediastinal/hilar lymph nodes, vasculature, and pericardium within the thorax. Mediastinal and hilar l...

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Ophthalmic manifestations in IgG4-related disease

IgG4-related disease (IgG4-RD) is characterized by variable tissue or organ involvements sharing common pathological findings. Orbital or orbital adnexa involvement of the disease has been reported in a few case series. The aim of our study was to characterize and analyze ophthalmic manifestations from a nationwide French case-series.Patients with IgG4-RD and orbital or orbital adnexa involveme...

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ژورنال

عنوان ژورنال: Current Treatment Options in Neurology

سال: 2017

ISSN: 1092-8480,1534-3138

DOI: 10.1007/s11940-017-0450-9