IgG4-Related Kidney Disease
Takao Saito · John H. Stone · Hitoshi Nakashima · Takako Saeki · Mitsuhiro Kawano
нов 2016. · Springer
E-knjiga
311
Stranica
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O ovoj e-knjizi
This book offers a detailed review of the pathological and imaging features, diagnosis and treatment of IgG4-Related Kidney Disease (IgG4-RKD). IgG4-related disease (IgG4-RD), which is characterized by an elevated serum IgG4 level and infiltration of systemic organs by IgG4 positive plasma cells, is a newly recognized systemic disease. Diverse renal manifestations including specific tubulointerstitial nephritis, membranous nephropathy, and tumor-like urological diseases extending to the pelvis and urinary tract in IgG4-RD have been reported and are recently attracting attention as IgG4-RKD. In this book, leading researchers in the field present the latest insights into the broad spectrum of IgG4-RKD characteristics. In addition, they provide a detailed explanation of the pathology of IgG4-RKD including comparisons between the kidney and other affected organs, such as the lacrimal, salivary glands and pancreas in the histopathological section. IgG4-Related Kidney Disease will have a major impact on future immunological and nephrological studies and offers a useful resource not only for nephrologists but also general physicians and investigators in related fields.
O autoru
Takao Saito, Emeritus Professor, Faculty of Medicine, Fukuoka UniversityJohn H. Stone, Massachusetts General Hospital Hitoshi Nakashima, Division of Nephrology & Rheumatology, Department of Internal Medicine, Fukuoka University Takako Saeki, Department of Internal Medicine, Nagaoka Red Cross Hospital Mitsuhiro Kawano, Division of Rheumatology, Department of Internal Medicine, Kanazawa University
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