Results 91 to 100 of about 609,847 (198)

IgG4-related inflammatory pseudotumor of the central nervous system responsive to mycophenolate mofetil

, 2012
Orbital apex and skull base masses often present with neuro-ophthalmic signs and symptoms. Though the localization of these syndromes and visualization of the responsible lesion on imaging is typically straightforward, definitive diagnosis usually relies
Thomas M. Coyne (6490292), Steven L. Galetta (4270588), Luis Mejico (7928264), Gustavo de la Roza (765859), Grant T. Liu (7928267), Heather E. Moss (3607835)   +5 more
core  

Periorbital presentation of IgG4 related disease

, 2018
IgG4-Related Disease is an immunomediated condition that is characterized by the presence of inflammatory lesions associated with fibrosis and lymphoplasmacytic infiltration rich in positive IgG4 tissue plasmocytes, forming a spectrum of ...
Gabriela Caroline Monteiro de Albuquerque (5911541), Rinalva Tenório Vaz (5911550), Bruna Dantas Aires Guimarães (5911544), Maria Amélia Silva de Sousa Ribeiro (5911547), Jerrar Janedson Xavier Silva (5911553)   +4 more
core   +1 more source

TREATMENT OF IgG4-RELATED DISEASE

, 2016
IgG4-related disease (IgG4-RD) is a fibroinflammatory condition characterized by the occurrence of tumor-like foci in different organs with a unique histological pattern (moirо-like fibrosis, obvious lymphoplasmacytic infiltration with large numbers of ...
V. I. Vasilyev, E. V. Sokol
core   +1 more source

IgG4-related chorioretinitis (a case report)

Офтальмохирургия, 2015
The IgG4-related disease is a specific inflammatory disorder characterized by the presence of elevated serum IgG4, inflammatory infiltrates rich of IgG4-positive plasma cells and subsequent fibrosis.
E. E. Grishina, I. A. Kazantseva, S. V. Lishchuk, A. A. Ryabtseva   +3 more
doaj  

Atypical IgG4 related hypophysitis revealed by submandibular sialadenitis: a case report

Endocrine Regulations
Objective. IgG4-related disease is a fibro-inflammatory multisystemic condition with lesions mimicking tumors. Involvement of the hypophysis is rare and the first case of IgG4-related hypophysitis was described in 2004.
Amor Bilel Ben, Hajji Ekram, Bayar Ines, Mesfar Rym, Saad Jamel, Njim Leila, Sayadi Hanene, Khochtali Ines   +7 more
doaj   +1 more source

Abundance of IgG4+ Plasma Cells in Isolated Reactive Lymphadenopathy Is No Indication of IgG4-Related Disease

, 2014
Contains fulltext : 138318.pdf (Publisher’s version ) (Open Access)OBJECTIVES: IgG4-related disease is a recently recognized condition that can be associated with lymphadenopathy, with several histologic patterns and increased absolute ...
Martinez, L.L., Laak, J.A.W.M. van der, Friedlander, E., Hebeda, K.M.   +3 more
core   +1 more source

Histological evolution of IgG4 related disease

Rheumatology & Autoimmunity, 2022
Subrahmanian Sathiavageesan, Anila Abraham   +1 more
doaj   +1 more source

IgG4-related disease in the nervous system [PDF]

IgG4-related disease (IgG4-RD) is a recently described multisystemic disorder the complete spectrum of which continues to be described. Nonetheless, distinct patterns of disease can be recognized.
Yang, Lu, Smith, Paul, Scolding, Neil J, Rice, Claire M   +3 more
core   +1 more source

Omics in IgG4-related disease

Chinese Medical Journal
Abstract Research on IgG4-related disease (IgG4-RD), an autoimmune condition recognized to be a unique disease entity only two decades ago, has processed from describing patients’ symptoms and signs to summarizing its critical pathological features, and further to investigating key pathogenic mechanisms. Challenges in gaining a
Shaozhe Cai, Yu Chen, Ziwei Hu, Shengyan Lin, Rongfen Gao, Bingxia Ming, Jixin Zhong, Wei Sun, Qian Chen, John H Stone, Lingli Dong, Xiangxiang Pan   +11 more
openaire   +3 more sources

Neurologic IgG4-Related Disease [PDF]

The Neurohospitalist, 2018
Karan, Topiwala, Christopher, Hampton, Carl, Boland, David, Waitzman   +3 more
openaire   +2 more sources