Results 41 to 50 of about 13,032,569 (265)

IgG4-Related Disease Manifested as Cutaneous Plasmacytosis: A Case Report

, 2023
Weijia Wang,1– 3 Xiaojing Kang,1– 3 Yuan Ding,1– 3 Lidan Mao,1– 3 Abudureyimu Dilinuer,1– 3 Wenzheng Li1– 3 1Department of Dermatology and Venereology, People’s Hospital of Xinjiang Uygur Autonomous Region, Urumqi, People’s Republic of China; 2Xinjiang ...
Li W, Dilinuer A, Kang X, Ding Y, Wang W, Mao L   +5 more
core  

IgG4-related disease [PDF]

, 2008
IgG4関連疾患は21世紀になって提唱された新しい疾患である｡組織学的にはIgG4陽性形質細胞やリンパ球浸潤が涙腺, 唾液腺, 後腹膜, 膵臓, 胆管などで起こり, 臨床的にはMikulicz病, 後腹膜線維症, 自己免疫膵炎, 糖尿病, 原発性硬化性胆管炎類似の胆管病変などを呈する全身性疾患であり, ステロイド治療に対する良好な反応性を認める｡その診断基準は確立されておらず, われわれは, ①血清IgG4の高値, ②本疾患に特徴的な臓器の障害(唾液腺,涙腺, 膵臓, 後腹膜 ...
Nakamura, Sukio, Hiramatsu, Kazuhisa, Matsushita, Koki, Miyoshi, Tomoko, Mizushima, Takaaki, Ochi, Koji, Asano, Motoi, Mitsunobu, Fumihiro, Koide, Norio, Kataoka, Hitomi   +9 more
core   +1 more source

IgG4-Related Disease Involving the Ear: A Case Report [PDF]

IgG4-related disease is a chronic inflammatory disease with widespread clinical presentation. It mimics various malignant, infectious, and inflammatory conditions, leading to confusion in diagnosis and management.
Ushant Acharya, Kripa Dongol, Rabindra Bhakta Pradhananga   +2 more
core   +1 more source

Диагностическая ценность IgG4 сыворотки крови при IgG4-связанном заболевании: так ли она велика? [PDF]

, 2019
IgG4-related disease (IgG4-RD) is a systemic immune mediated condition that is characterized by the formation of tumor-like fibroinflamma-tory foci in different organs and by the elevation of serum and tissue IgG4 levels in the majority of patients.
Е. В. Сокол, E. V. Sokol, A. V. Torgashina, M. V. Cherkasova, М. В. Черкасова, А. В. Торгашина   +5 more
core   +1 more source

Inebilizumab in AQP4‐Seropositive NMOSD: One‐Year Follow‐Up From a Multicenter, Real‐World Study

Annals of Clinical and Translational Neurology, EarlyView.
ABSTRACT Objective Real‐world evidence on inebilizumab among neuromyelitis optica spectrum disorder (NMOSD) patients is lacking. This study assessed inebilizumab among Chinese patients with aquaporin 4 autoantibody (AQP4‐IgG)‐seropositive NMOSD in a real‐world setting.
Mengcui Gui, Jiayang Zhan, Wei Li, Tao Jin, Dan He, Daishi Tian, Zhijun Li, Jing Lin, Yue Li, Hongyu Zhou, Bitao Bu   +10 more
wiley   +1 more source

IgG4-related sclerosing disease

World Journal of Gastroenterology, 2008
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 ...
Terumi, Kamisawa, Atsutake, Okamoto
openaire   +2 more sources

IgG4-related autoimmune liver disease

, 2023
The term IgG4-related autoimmune liver disease (AILD) refers to hepato-biliary manifestations of Immunoglobin G4-related disease (IgG4-RD) including IgG4-related sclerosing cholangitis and IgG4-related pseudotumor.
Pedica F., Palumbo D., Della-Torre E., Capurso G.   +3 more
core   +1 more source

Nanomaterials for Allergy Diagnosis and Treatment: Advances, Opportunities and Translational Challenges

Advanced Science, EarlyView.
Nanomaterials offer dual applications in allergy management. For diagnosis, nanomaterials enhance analytical sensitivity and improve detection in specific IgE and functional assays such as the basophil activation test (BAT). For allergen‐specific immunotherapy, nanomaterials enable allergen masking and controlled release, and effectively modulate the ...
Madiha Habib, Shan Jiang, Joyce ZX Lee, CW Lim, HL Yeung, Nicki YH Leung, Patrick SC Leung, Ting F Leung, Christine YY Wai   +8 more
wiley   +1 more source

IgG4-related lymphadenopathy – a difficult diagnosis

Surgical and Experimental Pathology, 2020
Background The IgG4-related disease (IgG4-RD) is a systemic immune-mediated non-neoplastic disease associated with IgG4 positive plasma cells and fibrosis that often presents as a mass lesion.
Balan Louis Gaspar
doaj   +1 more source

IgG4-related hypertensive granulomatous anterior uveitis

American Journal of Ophthalmology Case Reports, 2022
Purpose: To report a case of hypertensive granulomatous anterior uveitis in the setting of IgG4-related disease (IgG4-RD). Observations: A 69-year-old man presented with no light perception vision in both eyes and bilateral granulomatous anterior uveitis
Judy L. Chen, Mauranda Men, Bita V. Naini, Edmund Tsui   +3 more
doaj   +1 more source