IgG4-Associated Tubulointerstitial Nephritis: Two Case Reports and a Literature Review

التفاصيل البيبلوغرافية
العنوان: IgG4-Associated Tubulointerstitial Nephritis: Two Case Reports and a Literature Review
المؤلفون: Jun Hou, Xiaoqiang Ding, Fengqing Cai, Yi Fang, Hong Liu
المصدر: Internal Medicine. 51:2385-2391
بيانات النشر: Japanese Society of Internal Medicine, 2012.
سنة النشر: 2012
مصطلحات موضوعية: Male, China, Systemic disease, Pathology, medicine.medical_specialty, T-Lymphocytes, Kidney, Autoimmune Diseases, Adrenal Cortex Hormones, Cell Movement, parasitic diseases, Internal Medicine, medicine, Humans, skin and connective tissue diseases, Aged, Autoimmune disease, integumentary system, business.industry, fungi, General Medicine, Middle Aged, medicine.disease, Tubulointerstitial Nephritis, Treatment Outcome, Corticosteroid therapy, Immunoglobulin G, Nephritis, Interstitial, business, Infiltration (medical)
الوصف: IgG4-related systemic disease (IgG4-RSD) is an autoimmune disease that includes a wide variety of lesions. IgG4-RSD is characterized by high levels of serum IgG4, abundant levels of IgG4-positive plasma cells and T-lymphocyte infiltration in various organs. Tubulointerstitial nephritis (TIN) is a major finding when the kidneys are involved and is effectively treated with corticosteroid therapy. We herein describe two cases of IgG4-related TIN. Such cases have rarely been reported in China.
تدمد: 1349-7235
0918-2918
الوصول الحر: https://explore.openaire.eu/search/publication?articleId=doi_dedup___::4c11679d50f8c42c612f212dddaa5011Test
https://doi.org/10.2169/internalmedicine.51.7970Test
حقوق: OPEN
رقم الانضمام: edsair.doi.dedup.....4c11679d50f8c42c612f212dddaa5011
قاعدة البيانات: OpenAIRE