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IgG4-related disease / Kazuichi Okazaki, editor.

Contributor(s): Okazaki, Kazuichi, (1953-), editor literario
Material type: materialTypeLabelE-bookSeries: (Current topics in microbiology and immunology ; volume 401).Publisher: Cham, Switzerland : Springer, [2017]Description: 1 recurso en línea (vii, 128 páginas) : ilustraciones.ISBN: 3319525425; 9783319525426.Other title: Immunoglobulin G4-related disease.Subject: Enfermedades autoinmunesOnline resources: Acceso a este recurso digital (usuarios Universidad Europea de Madrid)Digital Resources
Contents:
Preface; Contents; 47 Current Concept of IgG4-Related Disease; Abstract; 1 The History of IgG4-Related Disease: Before and After Discovery of IgG4 (Table 1); 2 Current Concepts of IgG4-RD; 3 Nomenclatures and Individual Organ Manifestation of IgG4-RD; 3.1 Type 1 Autoimmune Pancreatitis (IgG4-Related Pancreatitis); 3.2 IgG4-Related Sclerosing Cholangitis (IgG4-SC); 3.3 IgG4-Related Dacryoadenitis and Sialoadenitis (Formerly Called Mikulicz's Disease); 3.4 IgG4-Related Ophthalmic Diseases (IgG4-Related OD); 3.5 IgG4-Related Kidney Disease (IgG4-Related KD)
3.2 Small-Scale GWAS for Detecting Genetic Factors Causing the Development of Lachrymal/Salivary Gland Lesions in AIP4 Conclusions and Future Perspectives; References; 38 The Histopathology of IgG4-Related Disease; Abstract; 1 Diagnosis of IgG4-Related Disease; 2 General Pathological Features of IgG4-RD; 2.1 Morphological Features; 2.2 Immunohistochemical Features; 3 Proposed Diagnostic Terminology for IgG4-RD; 4 Pancreatobiliary Manifestations; 5 Sialadenitis and Dacryoadenitis; 6 Lung Disease; 7 Periaortitis, Inflammatory Aneurysm, and Retroperitoneal Fibrosis; 8 Lymphadenopathy; 9 Summary
3.4 Treatment-Related Side Effects4 Prognosis; 5 Future Perspectives; References; 37 Immunogenetics of IgG4-Related AIP; Abstract; 1 Introduction; 2 Association Studies Using Polymorphic Markers in Candidate Genes; 2.1 Human Leukocyte Antigen (HLA) Complex; 2.2 Fc Receptor-Like 3 (FCRL3) Gene; 2.3 Cytotoxic T-Lymphocyte Antigen-4 (CTLA-4; CD152) Gene; 2.4 Toll-Like Receptor 4 (TLR4) and Protein Tyrosine Phosphatase N22 (PTPN22) Genes; 3 Association Studies Using Genome-Wide Polymorphic Markers; 3.1 Microsatellite Markers
3.6 IgG4-Related Retroperitoneal Fibrosis (IgG4-Related RPF)3.7 IgG4-Related Pulmonary Diseases (IgG4-Related PD); 3.8 IgG4-Related Thyroid Disease; 3.9 IgG4-Related Aortitis/Periaortitis; 3.10 IgG4-Related Lymphadenopathy; Acknowledgment; References; 36 Diagnosis and Treatment of IgG4-Related Disease; Abstract; 1 Introduction; 2 Diagnosis; 2.1 Epidemiology; 2.2 Clinical Symptoms; 2.3 Laboratory Tests; 2.4 Imaging; 2.5 Histopathology; 2.6 Steroid Responsiveness; 2.7 Diagnostic Criteria; 3 Treatment; 3.1 Indication of Treatment; 3.2 Induction of Remission; 3.3 Relapse and Maintenance Therapy
Abstract: This volume focuses on IgG4-related disease (IgG4-RD), a novel clinical entity involving multiple organs and of unknown origin, associated with the abundant infiltration of IgG4-positive cells. It consists of nine chapters written by prominent experts in the field and discusses the disease concept, diagnosis and treatment, as well as recent findings on its pathogenesis and pathophysiology. As such, it offers an invaluable source of information for researchers and clinicians alike.
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Holdings
Item type Current library Collection Call number Status Date due Barcode Item holds
LIBRO-E NO PRÉSTAMO LIBRO-E NO PRÉSTAMO Madrid Digital Acceso Electrónico (UEM) Ciencias de la Salud RC582 .I347 2017 EB (Browse shelf(Opens below)) Acceso electrónico eBook.20023287
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SpringerLink Springer Biomedical and Life Sciences eBooks 2017 English+International

Preface; Contents; 47 Current Concept of IgG4-Related Disease; Abstract; 1 The History of IgG4-Related Disease: Before and After Discovery of IgG4 (Table 1); 2 Current Concepts of IgG4-RD; 3 Nomenclatures and Individual Organ Manifestation of IgG4-RD; 3.1 Type 1 Autoimmune Pancreatitis (IgG4-Related Pancreatitis); 3.2 IgG4-Related Sclerosing Cholangitis (IgG4-SC); 3.3 IgG4-Related Dacryoadenitis and Sialoadenitis (Formerly Called Mikulicz's Disease); 3.4 IgG4-Related Ophthalmic Diseases (IgG4-Related OD); 3.5 IgG4-Related Kidney Disease (IgG4-Related KD)

3.2 Small-Scale GWAS for Detecting Genetic Factors Causing the Development of Lachrymal/Salivary Gland Lesions in AIP4 Conclusions and Future Perspectives; References; 38 The Histopathology of IgG4-Related Disease; Abstract; 1 Diagnosis of IgG4-Related Disease; 2 General Pathological Features of IgG4-RD; 2.1 Morphological Features; 2.2 Immunohistochemical Features; 3 Proposed Diagnostic Terminology for IgG4-RD; 4 Pancreatobiliary Manifestations; 5 Sialadenitis and Dacryoadenitis; 6 Lung Disease; 7 Periaortitis, Inflammatory Aneurysm, and Retroperitoneal Fibrosis; 8 Lymphadenopathy; 9 Summary

3.4 Treatment-Related Side Effects4 Prognosis; 5 Future Perspectives; References; 37 Immunogenetics of IgG4-Related AIP; Abstract; 1 Introduction; 2 Association Studies Using Polymorphic Markers in Candidate Genes; 2.1 Human Leukocyte Antigen (HLA) Complex; 2.2 Fc Receptor-Like 3 (FCRL3) Gene; 2.3 Cytotoxic T-Lymphocyte Antigen-4 (CTLA-4; CD152) Gene; 2.4 Toll-Like Receptor 4 (TLR4) and Protein Tyrosine Phosphatase N22 (PTPN22) Genes; 3 Association Studies Using Genome-Wide Polymorphic Markers; 3.1 Microsatellite Markers

3.6 IgG4-Related Retroperitoneal Fibrosis (IgG4-Related RPF)3.7 IgG4-Related Pulmonary Diseases (IgG4-Related PD); 3.8 IgG4-Related Thyroid Disease; 3.9 IgG4-Related Aortitis/Periaortitis; 3.10 IgG4-Related Lymphadenopathy; Acknowledgment; References; 36 Diagnosis and Treatment of IgG4-Related Disease; Abstract; 1 Introduction; 2 Diagnosis; 2.1 Epidemiology; 2.2 Clinical Symptoms; 2.3 Laboratory Tests; 2.4 Imaging; 2.5 Histopathology; 2.6 Steroid Responsiveness; 2.7 Diagnostic Criteria; 3 Treatment; 3.1 Indication of Treatment; 3.2 Induction of Remission; 3.3 Relapse and Maintenance Therapy

This volume focuses on IgG4-related disease (IgG4-RD), a novel clinical entity involving multiple organs and of unknown origin, associated with the abundant infiltration of IgG4-positive cells. It consists of nine chapters written by prominent experts in the field and discusses the disease concept, diagnosis and treatment, as well as recent findings on its pathogenesis and pathophysiology. As such, it offers an invaluable source of information for researchers and clinicians alike.

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