دانلود کتاب Diabetes Insipidus in Children: A Pocket Guide

فهرست مطالب :

Foreword Acknowledgments Introduction Contents Contributors 1: Primary Polydipsia Case Presentation Assessment and Diagnosis Management Complications References 2: Diagnosing DI (The Water Deprivation Test) Case Water Deprivation Test Concept History Limitations Additional Testing AVP Copeptin Patient Selection and Testing Protocol and Interpretation Preparation Prior To Admission On Admission At Any Time During the Test (See Fig. 2.1) Assessment of Response to Vasopressin Our Patient Summary References 3: MRI Lesions in Diabetes Insipidus Introduction Normal MRI Appearance of the Pituitary Gland (Fig. 3.1) MRI Findings in a Child with Diabetes Insipidus Langerhans Cell Histiocytosis (LCH) Hypophysitis Germ Cell Tumors (GCT) Rathke Cleft Cysts (RCC) Craniopharyngioma Other Tumors Congenital Abnormalities in the Pituitary/Hypothalamic Region Causing DI Ectopic Posterior Pituitary (EPP) Septo-optic Dysplasia (SOD) Inflammatory and Infectious Conditions Summary References 4: Central Diabetes Insipidus with Pituitary Stalk Thickening Case Description Assessment and Diagnosis Management Outcome References 5: Hypophysitis Vignette Chapter Write-Up Description/Incidence Classifications Difference from Adults Laboratory and Imaging Studies Histologic Findings Natural History Differential Treatment Utility of Autoantibodies Imaging Findings Over Time Anterior Pituitary Hormone Deficiency (APHD) Over Time Conclusion References 6: Germ Cell Tumors Case Presentation #1 Case Presentation #2 Discussion Management References 7: The Gist of a Rathke’s Cleft Cyst Case Clinical Impression after Initial Results and Consultation Bibliography 8: Langerhans Cell Histiocytosis and Diabetes Insipidus Clinical Case Presentation Case #1 Case #2 Introduction Presentation, Diagnosis, Classification, and Therapy Pituitary Involvement, Endocrine Dysfunction, and Neurodegeneration in LCH References 9: Craniopharyngioma and Diabetes Insipidus Case Presentation Assessment and Diagnosis Management Outcome References 10: Diabetes Insipidus After Craniopharyngioma Resection Case Presentation Discussion References 11: Partial Central Diabetes Insipidus Following Endonasal Biopsy Case Presentation Assessment and Diagnosis Management Outcome References 12: Septo-optic Dysplasia Spectrum Case Description Assessment and Diagnosis Management Outcome References 13: Familial DI and Genetic Workup Case Presentation Assessment and Diagnosis Management Outcome References 14: Treatment with Thiazides in Infants with Central Diabetes Insipidus Case Presentation Assessment and Diagnosis Management Outcome References 15: Absent Thirst and Diabetes Insipidus Case Presentation Assessment and Diagnosis Management Outcome References 16: Nephrogenic Diabetes Insipidus Case Discussion Congenital Nephrogenic DI AVPR2 Gene Mutations AQP2 Gene Mutations Current Management Approaches for NDI Nutrition Diuretics Non-steroidal Anti-inflammatory Drugs (NSAID) Possible Future Precision Medicine Through Targeted Gene Therapy Strategies Acquired NDI Amyloidosis Granuloma-Associated Conditions (Sarcoidosis and Histiocytosis) Sjogren Syndrome Sickle Cell Disease (SCD) Drugs Lithium Ifosfamide Foscarnet Antibiotics Other Disorders Associated with NDI Hypokalemia Fabry Disease References Index