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Oxford textbook of vasculitis / edited by Gene V. Ball, MD, Barri J. Fessler, MD, MSPH and S. Louis Bridges, Jr., MD, PhD.

Contributor(s): Material type: TextTextSeries: Oxford textbooks in rheumatology Oxford textbook of vasculitisPublisher: Oxford : Oxford University Press, 2014Edition: Third editionDescription: 1 online resourceContent type:
  • text
Media type:
  • computer
Carrier type:
  • online resource
ISBN:
  • 9780191667022
  • 0191667021
Other title:
  • Textbook of vasculitis
  • Vasculitis
Uniform titles:
  • Vasculitis.
Subject(s): Genre/Form: Additional physical formats: Print version:: Oxford textbook of vasculitis.DDC classification:
  • 616.13 23
LOC classification:
  • RC694.5.I53
Online resources:
Contents:
Cover; Oxford Textbook of Vasculitis; Copyright; Contents; Abbreviations; Contributors; SECTION 1 Introductory chapters; CHAPTER 1 Nomenclature and classification of vasculitic syndromes; CHAPTER 2 Epidemiology of vasculitis; SECTION 2 Basic science; CHAPTER 3 Hypersensitivity; CHAPTER 4 Biology of endothelial cells; CHAPTER 5 Complement in vasculitis; CHAPTER 6 Autoantibodies in vasculitis; CHAPTER 7 Pathogenesis of vasculitis; CHAPTER 8 Animal models of vasculitis; CHAPTER 9 Pathological features of vasculitis; SECTION 3 Clinical manifestations common to vasculitis.
CHAPTER 10 Cutaneous manifestations of vasculitisCHAPTER 11 Ocular manifestations of systemic vasculitis; CHAPTER 12 Cardiopulmonary manifestations of vasculitis; CHAPTER 13 Vasculitic neuropathy; CHAPTER 14 Vasculitic manifestations in the gastrointestinal tract; CHAPTER 15 Renal manifestations; CHAPTER 16 Digital ischaemia and Raynaud's phenomenon; SECTION 4 Imaging and percutaneous interventions; CHAPTER 17 Angiography and percutaneous interventions; CHAPTER 18 Cross-sectional imaging in vasculitis; CHAPTER 19 PET imaging in vasculitis.
SECTION 5 Vasculitic diseases and syndromes and related disordersCHAPTER 20 Approach to the diagnosis of vasculitis in adult patients; CHAPTER 21 Vasculitis in infancy, childhood, and adolescence; CHAPTER 22 Assessment of disease activity and damage; CHAPTER 23 Giant cell arteritis and polymyalgia rheumatica; CHAPTER 24 Takayasu's arteritis; CHAPTER 25 Polyarteritis nodosa; CHAPTER 26 Microscopic polyangiitis; CHAPTER 27 Cutaneous polyarteritis; CHAPTER 28 Kawasaki's disease; CHAPTER 29 Granulomatosis with polyangiitis (Wegener's granulomatosis): pathogenesis.
CHAPTER 30 Granulomatosis with polyangiitis (Wegener's granulomatosis): clinical and immunodiagnostic aspectsCHAPTER 31 Granulomatosis with polyangiitis (Wegener's granulomatosis): treatment; CHAPTER 32 Eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome); CHAPTER 33 Vasculitis in primary connective tissue diseases; CHAPTER 34 Behçet's syndrome: pathogenesis, clinical manifestations, and treatment; CHAPTER 35 Juvenile Behçet's syndrome; CHAPTER 36 Vasculitis of the central nervous system; CHAPTER 37 Thromboangiitis obliterans (Buerger's disease).
CHAPTER 38 Cutaneous small-vessel vasculitisCHAPTER 39 IgA vasculitis (Henoch-Schönlein purpura); CHAPTER 40 Cryoglobulinaemic vasculitis; CHAPTER 41 Miscellaneous forms of vasculitis; CHAPTER 42 Experimental therapies for vasculitis; SECTION 6 Mimickers of vasculitis; CHAPTER 43 Antiphospholipid syndrome; CHAPTER 44 Imitators of vasculitis; Index.
Summary: The third edition of this definitive and highly-regarded reference work provides a comprehensive review of vasculitis, a fascinating array of life-threatening and minor conditions caused by inflammatory syndromes and diseases that affect the blood vessels. The text uniquely brings together concepts from both the biological and clinical aspects of vasculitis. Research in clinical immunology now invigorates the entire area of vasculitis and shapes a rational approach to pathogenesis, diagnosis, and treatment, which is the substance of this text. Over 40 chapters cover known vasculitic conditions, and are illustrated with over 250 full-colour photographs of clinical and pathologic findings, diagrams, and tables.
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Previous edition: published as Vasculitis. 2008.

Print version record.

The third edition of this definitive and highly-regarded reference work provides a comprehensive review of vasculitis, a fascinating array of life-threatening and minor conditions caused by inflammatory syndromes and diseases that affect the blood vessels. The text uniquely brings together concepts from both the biological and clinical aspects of vasculitis. Research in clinical immunology now invigorates the entire area of vasculitis and shapes a rational approach to pathogenesis, diagnosis, and treatment, which is the substance of this text. Over 40 chapters cover known vasculitic conditions, and are illustrated with over 250 full-colour photographs of clinical and pathologic findings, diagrams, and tables.

Includes bibliographical references and index.

Cover; Oxford Textbook of Vasculitis; Copyright; Contents; Abbreviations; Contributors; SECTION 1 Introductory chapters; CHAPTER 1 Nomenclature and classification of vasculitic syndromes; CHAPTER 2 Epidemiology of vasculitis; SECTION 2 Basic science; CHAPTER 3 Hypersensitivity; CHAPTER 4 Biology of endothelial cells; CHAPTER 5 Complement in vasculitis; CHAPTER 6 Autoantibodies in vasculitis; CHAPTER 7 Pathogenesis of vasculitis; CHAPTER 8 Animal models of vasculitis; CHAPTER 9 Pathological features of vasculitis; SECTION 3 Clinical manifestations common to vasculitis.

CHAPTER 10 Cutaneous manifestations of vasculitisCHAPTER 11 Ocular manifestations of systemic vasculitis; CHAPTER 12 Cardiopulmonary manifestations of vasculitis; CHAPTER 13 Vasculitic neuropathy; CHAPTER 14 Vasculitic manifestations in the gastrointestinal tract; CHAPTER 15 Renal manifestations; CHAPTER 16 Digital ischaemia and Raynaud's phenomenon; SECTION 4 Imaging and percutaneous interventions; CHAPTER 17 Angiography and percutaneous interventions; CHAPTER 18 Cross-sectional imaging in vasculitis; CHAPTER 19 PET imaging in vasculitis.

SECTION 5 Vasculitic diseases and syndromes and related disordersCHAPTER 20 Approach to the diagnosis of vasculitis in adult patients; CHAPTER 21 Vasculitis in infancy, childhood, and adolescence; CHAPTER 22 Assessment of disease activity and damage; CHAPTER 23 Giant cell arteritis and polymyalgia rheumatica; CHAPTER 24 Takayasu's arteritis; CHAPTER 25 Polyarteritis nodosa; CHAPTER 26 Microscopic polyangiitis; CHAPTER 27 Cutaneous polyarteritis; CHAPTER 28 Kawasaki's disease; CHAPTER 29 Granulomatosis with polyangiitis (Wegener's granulomatosis): pathogenesis.

CHAPTER 30 Granulomatosis with polyangiitis (Wegener's granulomatosis): clinical and immunodiagnostic aspectsCHAPTER 31 Granulomatosis with polyangiitis (Wegener's granulomatosis): treatment; CHAPTER 32 Eosinophilic granulomatosis with polyangiitis (Churg-Strauss syndrome); CHAPTER 33 Vasculitis in primary connective tissue diseases; CHAPTER 34 Behçet's syndrome: pathogenesis, clinical manifestations, and treatment; CHAPTER 35 Juvenile Behçet's syndrome; CHAPTER 36 Vasculitis of the central nervous system; CHAPTER 37 Thromboangiitis obliterans (Buerger's disease).

CHAPTER 38 Cutaneous small-vessel vasculitisCHAPTER 39 IgA vasculitis (Henoch-Schönlein purpura); CHAPTER 40 Cryoglobulinaemic vasculitis; CHAPTER 41 Miscellaneous forms of vasculitis; CHAPTER 42 Experimental therapies for vasculitis; SECTION 6 Mimickers of vasculitis; CHAPTER 43 Antiphospholipid syndrome; CHAPTER 44 Imitators of vasculitis; Index.

English.

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