Search engine for discovering works of Art, research articles, and books related to Art and Culture
ShareThis
Javascript must be enabled to continue!

Rapidly Progressive Glomerulonephritis

View through CrossRef
Abstract Rapidly Progressive Glomerulonephritis is one of the most exciting areas in renal medicine. The disease usually presents acutely, and leads to end stage renal failure in weeks or months if untreated. However, appropriate immunosuppressive therapy can dramatically improve the prognosis in many cases, such that renal failure is avoided. It is now clear that various immunopathological processes are involved, and that an accurate diagnosis is of value in guiding management. This volume aims to bring together current knowledge of both scientific and clinical aspects of RPN. Recent advances in the immunology, inflammatory mechanisms and pathology of RPGN are discussed. This is followed by consideration of the major causes of RPGN, which include Goodpasture's disease, primary systemic vasculitis and systemic lupus erythematosus. RPGN secondary to other renal and systemic diseases, and RPGN in children are also described. Finally, new approaches to treatment are reviewed. Although certain of these areas are covered in the larger textbooks of renal medicine, our aim is to provide a current overview of RPGN, in a concise volume. This should be of particular interest to nephrologists and general physicians, including those in training, but may also be of value to pathologists, immunologists, and other studying the mechanisms of renal disease. We hope that this volume will help them in the management of patients with RPGN, or in planning their research into this condition.
Oxford University PressNew York, NY
Title: Rapidly Progressive Glomerulonephritis
Description:
Abstract Rapidly Progressive Glomerulonephritis is one of the most exciting areas in renal medicine.
The disease usually presents acutely, and leads to end stage renal failure in weeks or months if untreated.
However, appropriate immunosuppressive therapy can dramatically improve the prognosis in many cases, such that renal failure is avoided.
It is now clear that various immunopathological processes are involved, and that an accurate diagnosis is of value in guiding management.
This volume aims to bring together current knowledge of both scientific and clinical aspects of RPN.
Recent advances in the immunology, inflammatory mechanisms and pathology of RPGN are discussed.
This is followed by consideration of the major causes of RPGN, which include Goodpasture's disease, primary systemic vasculitis and systemic lupus erythematosus.
RPGN secondary to other renal and systemic diseases, and RPGN in children are also described.
Finally, new approaches to treatment are reviewed.
Although certain of these areas are covered in the larger textbooks of renal medicine, our aim is to provide a current overview of RPGN, in a concise volume.
This should be of particular interest to nephrologists and general physicians, including those in training, but may also be of value to pathologists, immunologists, and other studying the mechanisms of renal disease.
We hope that this volume will help them in the management of patients with RPGN, or in planning their research into this condition.

Related Results

Glomerulonephritis associated with endocarditis, deep-seated infections, and shunt nephritis
Glomerulonephritis associated with endocarditis, deep-seated infections, and shunt nephritis
Endocarditis is a cause of glomerulonephritis. Healthcare interventions (prosthetic valves, indwelling catheters, pacemaker wires) and intravenous drug abuse are presently the most...
Social Change Philanthrophy in America
Social Change Philanthrophy in America
Alan Rabinowitz provides the first comprehensive analysis of the nontraditional or social change philanthropists who help finance national campaigns and grassroots organizations th...
Creating a Female Dominion in American Reform 1890–1935
Creating a Female Dominion in American Reform 1890–1935
Abstract In this book, Muncy explains the continuity of white, middle-class, American female reform activity between the Progressive era and the New Deal. She argues...
Infectious complications renal disease
Infectious complications renal disease
Abstract This book considers the aetiological factors that render renal patients at risk of infection and covers the infectious complications of the major modalities...
Clinical features of ANCA-associated vasculitis
Clinical features of ANCA-associated vasculitis
The primary ANCA-associated vasculitides are granulomatosis with polyangiitis (Wegener's, GPA), microscopic polyangiitis (MPA), and eosinophilic granulomatosis with polyangiitis (E...
From Lancaster County to Lowville
From Lancaster County to Lowville
This chapter traces the arrival of four Old Order Amish families from the Path Valley in Pennsylvania to Lowville in Lewis County. More progressive than Swartzentruber and less pro...
Fabry disease
Fabry disease
Fabry disease is a rare X-linked lysosomal storage disorder in which deficiency of alpha-galactosidase A leads to accumulation of substrate, mostly globotriaosylceramide, which cau...
Fabry disease
Fabry disease
Fabry disease is a rare X-linked lysosomal storage disorder in which deficiency of alpha-galactosidase A leads to accumulation of substrate, mostly globotriaosylceramide (Gb3), whi...

Back to Top