Results 71 to 80 of about 13,032,569 (265)

The association of recurrent stroke and immunoglobulin G4-related arteritis in the central nervous system: a case report

Journal of Stroke and Cerebrovascular Diseases
Background: Immunoglobulin G4–related disease (IgG4-RD) is a systemic immune-mediated fibroinflammatory disease. Histopathology is the key to diagnosis.
Qi Huang, Hongjian Shen, Pengfei Xing, Yi Jiang, Xiaolong Xu, Qiang Li, Yongwei Zhang   +6 more
doaj   +1 more source

IgG4-positive Plasmocytosis of Inflammatory Cell Spreading Pattern Revealed to Differentiation in Classic Oral Lichen Planus [PDF]

, 2013
Objective:Oral lichen planus( OLP) is a chronic inflammatory oral mucosal disease of unknown etiology.Due to similar histological features of OLP with other oral diseases.
Imai, Yutaka, Fujimori, Takahiro, Kojima, Masaru, Hakata, Yuko, Imura, Johji, Maruoka, Takashi, Tomita, Shigeki, Ichikawa, Kazuhito   +7 more
core  

Glucocorticoids combined with rituximab treatment for IgG4-related tubulointerstitial nephritis with diabetic nephropathy: a case report

Open Medicine
IgG4-related disease is a chronic immune-mediated disorder featuring elevated serum IgG4 levels and the tissue infiltration of IgG4-positive plasma cells.
Wang Tianshu, Zhang Jingjing, Xu Yaguang
doaj   +1 more source

Refractory Eczema as a Presenting Feature of Common Variable Immunodeficiency

JEADV Clinical Practice, EarlyView.
ABSTRACT Common variable immunodeficiency (CVID) is the most prevalent symptomatic inborn error of immunity (IEI) in adults. It presents with recurrent infections and non‐infectious complications, including autoimmunity, lymphoproliferation and dermatitis.
Mercedes Sanchez‐Diaz, Lars Matthies, Andrea Vanegas Ramirez   +2 more
wiley   +1 more source

Plasma Cell Mucositis: A 20‐Year Retrospective Review at a Tertiary Center

JEADV Clinical Practice, EarlyView.
ABSTRACT Background Plasma cell mucositis (PCM) is a rare, chronic inflammatory condition of mucosal surfaces that is likely underdiagnosed and underreported, with limited data on its clinical characteristics, extracavitary involvement, and treatment outcomes.
Miguel A. Aristizabal‐Torres, Jessi M. Larrinaga, Katherine Bodiford, Olayemi Sokumbi, Leila Tolaymat   +4 more
wiley   +1 more source

Multisystem IgG4-related disease involving the abdomen and coronary arteries and causing chronic abdominal pain

Acta Radiologica Open, 2021
IgG4-related disease was originally discovered in patients with autoimmune pancreatitis accompanied by elevated serum IgG4 levels and has subsequently been described in almost every organ system.
Nam Ju Lee, James F Glockner
doaj   +1 more source

IgG4 Related Cardiac Disease [PDF]

Methodist DeBakey Cardiovascular Journal, 2013
IgG4-related systemic disease is an inflammatory disorder that can affect many organs. This case report describes a patient who in 2004 was found to have an inflammatory pseudotumor with IgG4 pathology. Over the next 3 years, visual symptoms responded well to recurrent courses of prednisone.
Hector, Carbajal, Lindsay, Waters, Jovan, Popovich, Milton, Boniuk, Patricia, Chevez-Barrios, Donald M, Marcus, Sandra, Sessoms   +6 more
openaire   +2 more sources

IgG4-RELATED DISEASE. CLINICAL NOTES [PDF]

, 2013
IgG4-related diseases are a new nosological entity that encompasses a few previously known diseases. IgG4-related systemic disease is diagnosed if two or more affected organs are detected.
E B Rodionova, N A Probatova, N V Kokosadze, E N Aleksandrova, T N Safonova, E L Nasonov, O A Logvinenko, S G Radenska-Lopovok, S Kh Sedyshev, Vladimir Ivanovich Vasilyev   +9 more
core   +1 more source

Angiosarcoma of the Scalp Presenting With Eyelid Edema: A Diagnostic Pitfall of Eyelid Biopsy

JEADV Clinical Practice, EarlyView.
ABSTRACT Angiosarcoma of the scalp is a rare but aggressive vascular malignancy that may present with nonspecific clinical findings, potentially leading to delayed diagnosis. Eyelid edema is an uncommon initial manifestation and has been suggested to result from direct tumor infiltration or lymphatic obstruction.
Sayo Komiyama, Sayaka Yamaguchi, Akiko Kaneshima, Aya Sunagawa, Shuhei Yonamine, Takuya Miyagi, Teruki Yanagi, Kenzo Takahashi   +7 more
wiley   +1 more source

A case of eosinophilic granulomatosis with polyangiitis complicated with a similar condition to IgG4 related lung disease

BMC Pulmonary Medicine, 2019
Background Atypical manifestations, such as elevated serum immunoglobulin-G4 (IgG4) and extra-pulmonary IgG4 positive plasmacyte infiltration, have been described in patients with eosinophilic granulomatosis with polyangiitis (EGPA), such complicated ...
Li Zhou, Fen Cao, Songqing Fan, Ping Chen, Shuizi Ding, Guiqian Liu, Ruoyun Ouyang   +6 more
doaj   +1 more source