Results 81 to 90 of about 232,932 (206)
JAK Inhibition as a Therapeutic Strategy for IgG4-RD [PDF]
Journal of Investigational Allergology and Clinical Immunology, 2021 S, Khan, P, Gordins, S, Durairaj
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Journal of Hepato-Biliary-Pancreatic Sciences, Volume 33, Issue 7, Page 557-567, July 2026.Kuraishi and colleagues showed that nearly one‐third of patients with type 1 autoimmune pancreatitis initially managed without corticosteroids eventually required steroid therapy. Elevated serum IgG4 predicted delayed steroid initiation, whereas spontaneous remission was associated with a lower likelihood of treatment, supporting careful risk ...
Yasuhiro Kuraishi +9 more
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Respirology Case Reports, Volume 14, Issue 7, July 2026.Multisystem IgG4‐RD can closely mimic metastatic malignancy and should be considered when thoracic and extrapulmonary mass‐forming lesions coexist. Timely biopsy confirmation is essential to avoid misdiagnosis and treatment delay. ABSTRACT IgG4‐related disease (IgG4‐RD) is a multisystem fibroinflammatory condition that can mimic metastatic malignancy ...
Ho Young Lee, Juyeon Kang
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Случай изолированного IgG4-связанного заболевания легких у подростка [PDF]
, 2020 IgG4-related disease (IgG4-RD) is a rare immune-mediated fibroinflammatory disease that is characterized by the occurrence of nodules in one or more organs and proceeds in most patients with the elevated levels of IgG4 in serum and/or in the tissues of ...
V. I. Vasilyev +5 more
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Histopathology, Volume 89, Issue 1, Page 47-57, July 2026.We report a series of 12 patients (mean age 63 years) with chronic oesophageal ulceration showing morphological features of IgG4‐related inflammatory disease. Most patients underwent several rounds of endoscopy until this association was recognized. The majority of patients went into clinical and histological remission following corticosteroid therapy.
Hanna Henzinger +5 more
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Internal Medicine Journal, Volume 56, Issue 7, Page 1218-1239, July 2026.Abstract Idiopathic multicentric Castleman disease (iMCD) is a rare condition. The pathogenesis is incompletely understood; however, interleukin‐6 (IL‐6) is a major mediator. The clinical presentation is heterogeneous, from mild constitutional symptoms to severe multi‐organ failure.
Dipti Talaulikar +16 more
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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 +5 more
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Arthritis Research & Therapy, 2021 Objective The growing utilization of needle biopsy has challenged the current pathology consensus of IgG4-related disease (IgG4-RD). The aims of this study were to identify the histological characteristics of needle biopsy and surgical specimens and ...
Yanying Liu +7 more
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Rheumatological aspects of IgG4-related disease (IgG4-RD)
Rheumatology (Bulgaria), 2023 Abstract. Immunoglobulin G4-related disease (IgG4-RD) is an immune-mediated fibro-inflammatory disorder, characterized by a tissue IgG4(+)plasma cells infiltration, leading to fibrosis and destruction of the involved organs. The IgG4-RD scope includes all organs and systems but within the review only the actual diagnostic and therapeutic data ...
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ERDHEIM‐Chester Disease: Two Fatal Cases With Unusual Presentations
Clinical Case Reports, Volume 14, Issue 6, June 2026.Fluorodeoxyglucose positron emission tomography‐computed tomography (FDG PET‐CT) demonstrated markedly increased metabolic activity in serosal surfaces including pericardium, pleura, and renal fascia, as well as diffuse uptake along vascular walls, particularly the entire aorta.
Ribero‐Vargas Daniel Andres +2 more
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