Primary and Secondary Immunodeficiency (eBook, PDF)

A Case-Based Guide to Evaluation and Management

• Format: PDF

Produktbeschreibung

This book provides a broad clinical overview of primary and secondary immunodeficiencies nested in clinical cases that will help the reader understand the approach to evaluation, diagnosis, and management of these challenging cases. Chapters begin with a comprehensive overview of immunodeficiencies to ground the reader in practical knowledge of the field and these complex conditions. Chapters cover B lymphocyte immunodeficiency, T cell immunodeficiency, immune dysregulation syndromes, and innate immune defects. They discuss a range of treatment options including gene therapy or bone marrow transplant. The book continues with a discussion on secondary immunodeficiencies and their treatment. Each chapter was written by authors with expertise related to different immunodeficiency disorders and provide a succinct overview of pathomechanisms, diagnosis, and treatment of a specific condition.

Primary and Secondary Immunodeficiency will be an excellent resource forpracticing allergists, hematologists, clinical immunologists, fellows, residents, and other clinicians who work with immunodeficiency patients.

Produktdetails

• Verlag: Springer International Publishing
• Erscheinungstermin: 28. Januar 2021
• Englisch
• ISBN-13: 9783030571573
• Artikelnr.: 61096879

Autorenporträt

Jonathan A. Bernstein, M.D. Professor of Clinical Medicine University of Cincinnati College of Medicine
Internal Medicine, Division of Immunology/Allergy Section
231 Albert Sabin Way, ML#563
Cincinnati, Ohio 45267
[e-mail]

Inhaltsangabe

Chapter 1. Overview of Immunodeficiency.- Part I. B-Lymphocyte Immunodeficiency.- Chapter 2. Common Variable Immunodeficiency, Hypogammaglobulinemia, and Specific Antibody Deficiency.- Chapter 3. Agammaglobulinemia.- Chapter 4. Class Switch Defects.- Chapter 5. Transient Immunodeficiency of Infancy.- Chapter 6. Selective Isotype Immunodeficiency.- Chapter 7. Common Variable Immunodeficiency Disorders-like Disorders.- Part II. T-Cell Immunodeficiency.- Chapter 8. Severe Combined Immunodeficiency.- Chapter 9. Idiopathic CD4 Lymphopenia.- Chapter 10. Hyper IgE Syndrome.- Chapter 11. Genetic Syndromes with Associated Immunodeficiencies.- Part III. Immune Dysregulation Syndromes.- Chapter 12. Autoimmune Lymphoproliferative Syndrome.- Chapter 13. Auto-inflammatory Syndromes.- Chapter 14. Immune Dysregulation Leading to Autoimmunity.- Chapter 15. Dendritic Cells in PrimaryImmunodeficiency.- Part IV. Innate Immune Defects.- Chapter 16. Congenital Neutropenia and Migration Defects.- Chapter 17. Chronic Granulomatous Disease.- Chapter 18. Primary Immunodeficiencies of Complement.- Chapter 19. Natural Killer Cell Defects.- Chapter 20. Mucocutaneous Candidiasis.- Part V. Secondary Immunodeficiency.- Chapter 21. Immunodeficiency Secondary to Malignancies and Biologics.- Chapter 22. Immunodeficiency Secondary to Prematurity, Pregnancy, and Aging.- Chapter 23. Vaccinations in Primary and Secondary Immunodeficiencies Including Asplenia.

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Chapter 1. Overview of Immunodeficiency.
 Part I.  B
Lymphocyte Immunodeficiency.
 Chapter 2. Common Variable Immunodeficiency, Hypogammaglobulinemia, and Specific Antibody Deficiency.
 Chapter 3. Agammaglobulinemia.
 Chapter 4. Class Switch Defects.
 Chapter 5. Transient Immunodeficiency of Infancy.
Chapter 6. Selective Isotype Immunodeficiency.
 Chapter 7. Common Variable Immunodeficiency Disorders
like Disorders.
 Part II. T
Cell Immunodeficiency.
 Chapter 8. Severe Combined Immunodeficiency.
 Chapter 9. Idiopathic CD4 Lymphopenia.
 Chapter 10. Hyper IgE Syndrome.
 Chapter 11.  Genetic Syndromes with Associated Immunodeficiencies.
 Part III. Immune Dysregulation Syndromes.
 Chapter 12. Autoimmune Lymphoproliferative Syndrome.
 Chapter 13. Auto
inflammatory Syndromes.
 Chapter 14. Immune Dysregulation Leading to Autoimmunity.
 Chapter 15. Dendritic Cells in PrimaryImmunodeficiency.
 Part IV. Innate Immune Defects.
 Chapter 16. Congenital Neutropenia and Migration Defects.
 Chapter 17. Chronic Granulomatous Disease.
 Chapter 18. Primary Immunodeficiencies of Complement.
 Chapter 19. Natural Killer Cell Defects.
 Chapter 20.  Mucocutaneous Candidiasis.
 Part V. Secondary Immunodeficiency.
 Chapter 21. Immunodeficiency Secondary to Malignancies and Biologics.
 Chapter 22.  Immunodeficiency Secondary to Prematurity, Pregnancy, and Aging.
 Chapter 23. Vaccinations in Primary and Secondary Immunodeficiencies Including Asplenia.