Neuroepidemiology in Tropical Health

Author: Preux   Pierre-Marie;Dumas   Michel  

Publisher: Elsevier Science‎

Publication year: 2017

E-ISBN: 9780128046258

P-ISBN(Paperback): 9780128046074

Subject: R741 Neurology

Keyword: 神经科学,神经病学与精神病学

Language: ENG

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Disclaimer: Any content in publications that violate the sovereignty, the constitution or regulations of the PRC is not accepted or approved by CNPIEC.

Description

Neuroepidemiology in Tropical Health covers major neurological diseases of relevance in tropical settings and examines the specificities of epidemiology of neurological diseases in the context of tropical countries that face many challenges when compared to the developed world. Part One focuses on methods and their eventual specificities, and how such methods, like sampling, can be adapted for specific scenarios. Parts Two and Three discuss environmental factors and their consequences for neurology in the tropical world, as well as large geographical areas and their specificities. Finally, Part Four presents relevant neurological diseases in in-depth chapters.

This invaluable information will help readers recognize the various neurological conditions presented, with the inclusion of their aetiologies and treatment in tropical areas. The book therefore fills a gap in the neuroepidemiology literature, with chapters written by an international collection of experienced authors in the field.

  • Highlights differences and similarities between neuroepidemiology in tropical areas and temperate zones with a focus on methods and underlying factors
  • Covers environmental factors in the tropical world and their consequences for neurology
  • Chapters include references (key articles, books, protocols) for additional detailed study
  • Includes wide topics of neurological disease in the tropics, not only infectious diseases, but also nutrition and

Chapter

References

I. Fundamental Concepts

1 Methodological Challenges of Neuroepidemiological Studies in Low- and Middle-Income Countries

1.1 Introduction

1.2 Study design and Feasibility in the Field

1.3 General Context

1.3.1 Geographical Difficulties

1.3.2 How to Move Forward?

1.3.3 Systematic Review and Meta-Analysis

1.3.4 Socioeconomic and Sociocultural Factors

1.4 Difficulties in the Availability and Mobilization of Data

1.4.1 Medical Data

1.4.2 General Population Census

1.4.3 Cartography and Geographical Information Systems

1.5 Study Design

1.5.1 Geographical and Logistical Challenges

1.5.2 Demographic and Follow-Up Issues

1.6 Clinical and Regulatory Issues

1.6.1 International Ethic Rules

1.6.2 Suspected Cases Ascertainment

1.6.3 Diagnostic and Treatment

1.7 Design-Specific Issues

1.7.1 Cases Census and Sample Studies

1.7.2 Involvement of Institutions and Key Stakeholders

1.7.3 Medical Examinations, Biological Specimens and Laboratory Tests

1.7.4 Monitoring and New Technologies

1.8 Valorization: Scientific and Public Health Issues

1.8.1 International Acknowledgments of the Works Conducted in Tropical Areas

1.8.2 Advocacy—Policy and International Cooperation

1.9 Conclusion

References

II. Tropical Neuroepidemiology: Between Environment and Genetics

2 Sociocultural Factors

2.1 Introduction

2.2 Tropical Neuroepidemiology and Health Anthropology: For Effective Collaboration

2.2.1 The Expected and Assumed Collaborative Epidemiology/Anthropology

2.2.2 A Concept: Almost Exclusive Use of the Sociocultural Representation Theory

2.2.3 Health-Related Stigma

2.3 Mental Disorders and Traditional Beliefs in SSA

2.3.1 Explanatory Models of Mental Illness in SSA

2.3.1.1 What are the Theories of Mankind in SSA?

2.3.1.2 Causality of Mental Illness in SSA

2.3.1.3 Psychosis and Neurosis

2.3.1.4 Stigma and Mental Illness

2.3.1.5 Managing Mental Illness: Traditional or Modern Medicine?

2.4 Sociocultural Representations and Stigma in Epilepsy

2.4.1 Explanatory Models of Epilepsy

2.4.2 Symptomatic Denominations

2.4.3 Etiological Denominations

2.4.4 Beliefs About Epilepsy in SSA

2.4.4.1 Magical Causes (Evil-Spirit, Possession, and Witchcraft)

2.4.4.2 Contagion

2.4.4.3 “Biomedical Model”: Foreign Body Migration, Body Fluids-Bound, and Heredity

2.4.4.4 Epilepsy and Stigma

2.5 Sociocultural Representations and Stigma in Dementia

2.5.1 Models of Understanding of Dementia

2.5.2 Social Tolerance of People With Dementia: Representations and Stigma

2.6 Conclusion

References

Further Reading

3 Climatic Factors Under the Tropics

3.1 Introduction

3.2 A Physical Geographic Approach: The Climate and Its Characteristics

3.2.1 The Role of the Inter-Tropical Convergence Zone

3.2.2 Types of Tropical Climate

3.3 A Biogeographical Approach: How Climate’s Features Determine Natural Biomes and Ecosystems

3.3.1 The Marine Biome

3.3.2 Microbial Diversity and Biogeography

3.4 Biology: Adaptation and Acclimation to Tropical Climates

3.4.1 Thermal Tolerance

3.4.2 Water Availability

3.4.3 UVR and Airborne Propagation of Neurotropic Viruses

3.4.4 Thermoregulation in Man

3.4.5 Nutrition

3.5 Does the Tropical Climate Favor Pathogens and Infections in Humans?

3.5.1 Biogeography

3.5.2 Role of Environmental Conditions

3.5.3 Infections of Humans

3.5.4 Seasonality Under the Tropics

3.5.5 The Tropical Origin of Infectious Diseases

3.5.6 Fungal Proliferation Under the Tropics

3.5.7 Algal Blooms and Seafood Poisoning

3.6 Weather Events and Extreme Effects of Climate

3.7 A Health Geographical Approach: Case Studies of Climatic Features that Modulate Tropical Diseases

3.7.1 Mainly Climatic Determinants

3.7.1.1 Epidemic Meningococcal Meningitis

3.7.2 Complex Relations Between Climate, Soil, and Human Activities

3.7.2.1 Climate Impact on Tropical Endemic Diseases Vectors Ecology: Case Studies of Malaria and Human African Trypanosomia...

3.7.2.2 The Amazon Basin, Soil Chemical Composition, Soil–Air Interface, Climate Dependency, and Environmental (Surface Wat...

3.8 The “Boomerang Effect” Under the Tropics: Health Consequences of Anthropogenic Changes

3.8.1 The Bangladesh Story: Persistent Dryness, Safe Drinking Water Availability and Deep-Water Wells

3.8.2 Agriculture Under the Tropics

3.8.3 Perturbation of the Global Nutrient Cycles

3.8.4 Climate in Tropical Cities

3.9 Conclusions

References

Further Reading

4 Economic Aspects

4.1 Introduction

4.2 Health System Financing: Key Challenges

4.2.1 The Changing Landscape of Disease and Injury

4.2.2 Health Spending: Inefficient or Insufficient?

4.2.3 Composition of Health Spending

4.3 Economical Aspects Related to Chronic Neurological Diseases

4.3.1 Epilepsy

4.3.2 Dementia and Cognitive Disorders

4.3.2.1 The Global Burden of Disease Approach

4.3.2.2 Limitations of the GBD Approach

4.3.2.3 Alternative Approaches to Understanding the Economic Impact of Dementia

4.4 Conclusion

References

5 Tropical Epidemiology: Nutritional Factors

5.1 Introduction

5.2 The Tools for Pointing Out Malnutrition and Obesity and Their Thresholds

5.2.1 Body Mass Index

5.2.2 Unintentional Loss of Weight

5.2.3 Main Other Anthopometric Assessments

5.2.4 Albuminemia

5.2.5 Dietician Survey

5.3 The Main Causes of Malnutrition During Neurological Diseases and Their Treatment

5.3.1 Disabilities

5.3.2 Anorexia

5.3.3 Swallowing Disorders

5.3.4 Disorders of Salivation

5.3.5 The Increase in Energy Expenditure

5.3.6 The Role of Therapeutics

5.4 Nutrition and Epilepsy in Tropical Countries

5.4.1 Malnutrition or Obesity as Possible Consequences of Epilepsy

5.4.2 Epilepsy Favored by Malnutrition

5.5 Nutrition and Dementia in Tropical Countries

5.5.1 Nutritional Status

5.5.2 Nutritional Factors Associated With Dementia

5.5.2.1 Malnutrition and Weight Loss

5.5.2.2 Food Consumption

References

6 Genetics of Infections and Diseases Caused by Human Parasites Affecting the Central Nervous System

6.1 Introduction

6.2 Neurocysticercosis

6.3 Toxoplasmosis

6.4 Cerebral Malaria

References

III. Tropical Neuroepidemiology by Large Areas of the World

7 Asia

7.1 Introduction

7.2 Stroke

7.2.1 Incidence, Prevalence, and Mortality

7.2.2 Stroke Subtypes

7.2.3 Young Stroke

7.2.4 Other Causes of Stroke

7.3 Epilepsy

7.3.1 Prevalence and Incidence

7.3.2 Classification and Causes

7.3.3 Mortality

7.3.4 Psychosocial Burden

7.3.5 Treatment Gap

7.3.6 Steven–Johnson Syndrome Secondary to Carbamazepine

7.4 Headache

7.4.1 Prevalence of Primary Headache

7.4.2 Headache in the Elderly

7.4.3 Cultural Influence on Concepts and Management

7.5 Neuroinflammation

7.5.1 Multiple Sclerosis

7.5.2 Neuromyelitis Optica

7.6 Neuromuscular Disorders

7.6.1 Amyotrophic Lateral Sclerosis

7.6.2 Guillain–Barré Syndrome

7.6.3 Myasthenia Gravis

7.6.4 Muscle Diseases

7.6.5 Toxic Neuropathies

7.7 Movement Disorders

7.7.1 Parkinson’s Disease

7.7.2 Atypical Parkinsonian Syndromes

7.7.3 Huntington’s Disease

7.7.4 Other Movement Disorders

7.8 Dementia

7.8.1 Dementia Subtypes

7.9 CNS Infections

7.9.1 Bacteria

7.9.2 Viruses

7.9.3 Parasites

7.9.4 Fungus

7.10 Neurology Care

7.10.1 Number of Neurologists

7.10.2 Neuroimaging, Clinical Neurophysiology Services, and Pharmaceuticals

7.10.3 Training Programs for Neurologists

7.10.4 Regional Networking and Publication

References

8 Neurologic Diseases in Tropical Oceania

8.1 Preamble

8.2 Tropical Australia

8.2.1 Overview

8.2.2 Geography and Health Resources

8.2.2.1 The Northern Territory

8.2.2.2 Queensland and Far North Queensland

8.2.2.3 The Kimberleys and North Western Australia

8.2.3 Indigenous Health

8.2.4 Neurology in Tropical Australia

8.2.4.1 Infectious Diseases: Protozoal and Nematode Infections

8.2.4.1.1 Malaria

8.2.4.1.2 Nematode-Induced Myositis

8.2.4.2 Infectious Diseases: Vector-Borne Viral Infections

8.2.4.2.1 Flaviviral Infections

Host Immunity

Target Populations

Neurological Features of Flaviviral Infections

Diagnosis of Flaviviral Infection

Treatment

Epidemiology of Arboviruses

Climate and Animal Vectors and Other Modes of Transmission

Seroprevalence

8.2.4.2.2 Murray Valley Encephalitis Virus

8.2.4.2.3 Kunjin Virus

8.2.4.2.4 Dengue Fever

Clinical Features

8.2.4.2.5 Japanese Encephalitis Virus

8.2.4.2.6 Newer Viral Infections Associated With Encephalitis

8.2.4.3.1 Melioidosis

Epidemiology

Clinical Picture

Pathology

8.2.4.3.2 Cryptococcus

8.2.4.3.3 Naegleria

8.2.4.3.4 Echinococcus

8.2.4.4 Non-infectious Neurological Diseases

8.2.4.4.1 Kava

8.2.4.4.2 Inhalants

8.2.5 Cerebrovascular Disease

8.2.6 Rheumatic Fever and Rhematic Heart Disease

8.2.7 Otitis Media

8.3 Melanesia

8.3.1 Papua New Guinea

8.3.1.1 Trauma

8.3.1.2 Vector-Borne Viral Disease

8.3.1.2.1 Malaria

8.3.1.2.2 Zika Virus

8.3.1.2.3 Kuru

8.3.1.2.4 Cysticercosis

8.3.2 New Caledonia

8.3.3 Fiji

8.4 Micronesia

8.4.1 Guam

8.4.1.1 ALS–Parkinsonism–Dementia Complex

8.4.2 Marshall Islands

8.4.3 Kiribati and Nauru

8.5 Polynesia

8.5.1 Samoa and Tonga

8.6 Cerebrovascular Disease in Oceania Outside Australia

8.7 The Future

Acknowledgments

References and Selected Reading

Newer Viral Encephalitides

Murray Valley Encephalitis

Dengue Fever

Melioidosis

Neurocysticercosis

Malaria

9 Neuroepidemiology in Latin America

9.1 Introduction

9.2 Neuroepidemiology in Latin America

9.3 Epilepsy

9.4 Multiple Sclerosis

9.5 Dementia Syndromes

9.6 Stroke

9.7 Headache and Migraine

9.8 Extrapyramidal Disease and Parkinson’s Diseases

9.9 ALS

9.10 Neuroinfectious Diseases

9.11 Neuroepidemiology Training and Education

9.12 Conclusions

References

10 Epidemiology of Neurological Disorders in Sub-Saharan Africa

10.1 Introduction

10.2 Infections of the Nervous System

10.2.1 HIV-Related Neurological Diseases

10.2.2 Neurosyphilis

10.2.3 Poliomyelitis

10.2.4 Leprosy

10.2.5 Tuberculous Spondylitis

10.3 Tropical Spastic Paraparesis

10.4 Neurofluorosis

10.5 Konzo

10.6 Stroke

10.7 Epilepsy

10.7.1 Etiologies of Epilepsy

10.7.1.1 CNS Infections

10.7.1.2 Birth Complications

10.7.1.3 Febrile Convulsions

10.7.1.4 Head Injuries

10.7.2 Genetic Factors

10.7.3 Burden

10.7.4 Prognosis

10.7.5 Treatment Options

10.8 Nodding Syndrome

10.9 Lathyrism

10.10 Dementia

10.11 Peripheral Neuropathies

10.12 Parkinson’s Disease

10.13 Conclusion

References

IV. Focus on Specific Neurological Syndromes or Diseases in Tropical Areas

11 Epilepsy

11.1 Introduction

11.2 Definitions

11.2.1 Epileptic Seizures

11.2.2 Epilepsy

11.3 Classification

11.3.1 Classification of Epilepsies and Epileptic Syndromes

11.3.2 Classification by Seizure Type

11.3.2.1 Focal Seizures

11.3.2.2 Generalized Seizures

11.3.2.2.1 Generalized Convulsive Seizures

11.3.2.2.2 Absence Seizures

11.3.2.2.3 Other Motor Seizures

11.3.2.2.4 Unclassifiable Seizures

11.4 Epidemiology

11.4.1 Methodological Considerations

11.4.1.1 Difficulties With Identification

11.4.1.2 Definition

11.4.1.3 The Problem of Diagnosis

11.4.2 The Prevalence of Epilepsy

11.4.3 The Incidence of Epilepsy

11.4.4 Seizure Type

11.5 The Causes of Epilepsy

11.5.1 Identifying the Etiology

11.5.2 Infection of CNS

11.5.2.1 Acute Bacterial Meningitis

11.5.2.2 Other Bacterial Suppurative Infections

11.5.2.3 Tuberculosis

11.5.2.4 Parasitic

11.5.2.5 Viral Infections

11.5.2.5.1 Human Immunodeficiency Virus

11.5.3 Traumatic Brain Injury

11.5.4 Perinatal Factors

11.5.5 Cerebrovascular Disease

11.5.6 Tumors

11.5.7 Family History of Epilepsy

11.6 Comorbidity

11.7 Mortality

11.8 Sociocultural Aspects

11.9 Treatment

11.10 Conclusion

References

12 Dementia

12.1 Background

12.1.1 Brain Pathology

12.1.2 Burden

12.1.3 Prevention

12.1.4 An Aging and Changing World

12.2 Prevalence

12.2.1 Asia

12.2.2 Latin America and Caribbean

12.2.3 Sub-Saharan Africa

12.3 Incidence

12.3.1 Asia

12.3.2 Latin America and the Caribbean

12.3.3 Sub-Saharan Africa

12.4 Mortality

12.5 Trends

References

13 Other Neurocognitive Disorders in Tropical Health (Amyotrophic Lateral Sclerosis and Parkinson’s Disease)

13.1 Introduction

13.2 Clinical Features of ALS

13.2.1 Introduction

13.2.2 Clinical Symptoms and Signs

13.3 Clinical Features of Parkinsonian Disorders

13.3.1 Introduction

13.3.2 Clinical Features

13.3.3 Diagnostic Criteria

13.4 Epidemiology of ALS

13.4.1 Study of ALS in Tropical Areas, a Challenging Context

13.4.2 ALS Variability With Population’s Ancestral Origin

13.4.3 ALS in Africa

13.4.4 ALS in Oceania

13.4.5 ALS in Asia

13.4.6 ALS in Latin America

13.5 Epidemiology of PD

13.5.1 Prevalence of Parkinsonism in Tropical Countries

13.5.2 Hypothesis for the Lower Frequency of PD in Tropical Countries

13.5.2.1 Racial or Ethnic Differences?

13.5.3 Higher Proportion of Atypical Parkinsonism?

13.5.4 Environmental Exposures?

13.6 Conclusion

References

14 Vascular Disorders

14.1 Introduction

14.2 Burden of Stroke in SSA

14.2.1 Overview

14.2.2 Epidemiology

14.2.2.1 Prevalence

14.2.2.2 Incidence

14.2.2.3 Mortality

14.2.2.4 Stroke Case-Fatality

14.2.2.5 Stroke Subtypes

14.2.3 Comments

14.3 Risk Factors

14.4 The Gaps

References

15 Neuromuscular Disorders in Tropical Areas

15.1 Introduction

15.2 Infectious NMDs

15.2.1 Bacterial Infections

15.2.1.1 Leprosy

15.2.1.2 Buruli Ulcer

15.2.1.3 Tuberculosis

15.2.1.4 Brucellosis

15.2.1.5 Tropical Pyomyositis

15.2.1.6 Leptospirosis and Other Spirochetes

15.2.1.7 Rickettsiosis

15.2.1.8 Diphtheria

15.2.1.9 Botulism

15.2.1.10 Tetanus

15.2.1.11 Typhoid Fever

15.2.2 Viral Infections

15.2.2.1 Human Immunodeficiency Virus

15.2.2.2 The Neurotropic Herpes Viruses

15.2.2.3 Cytomegalovirus

15.2.2.4 Human T-lymphotropic Virus 1

15.2.2.5 The Hepatitis Viruses

15.2.2.6 Arboviruses

15.2.2.7 Poliovirus

15.2.2.8 Rabies

15.2.2.9 Rubella

15.2.2.10 Influenza

15.2.3 Parasitic and Fungal Infections

15.2.3.1 American Trypanosomiasis

15.2.3.2 Trichinellosis (or Trichinosis)

15.2.3.3 Cysticercosis

15.2.3.4 Echinococcosis

15.2.3.5 Schistosomiasis (or Bilharziasis)

15.2.3.6 Malaria

15.2.3.7 Gnathosomiasis

15.2.3.8 Angiostrongyliasis

15.2.3.9 Dracunculiasis

15.2.3.10 Infection by Haycocknema perplexum

15.2.3.11 Coenuriasis

15.2.3.12 Toxoplasmosis

15.2.3.13 Onchocerciasis

15.2.3.14 Giardiasis

15.2.3.15 Bothriocephalus Infection

15.2.3.16 Leishmaniasis

15.2.3.17 Sarcocystosis

15.2.3.18 Microsporidial Infections

15.3 Malnutrition and Micronutrient Deficiencies

15.3.1 Vitamin B1 (Thiamin) Deficiency

15.3.2 Vitamin B2 (Riboflavin) Deficiency

15.3.3 Vitamin B3 (Niacin) Deficiency

15.3.4 Vitamin B5 (Pantothenic Acid) Deficiency

15.3.5 Vitamin B6 (Pyridoxine) Deficiency

15.3.6 Vitamin B8 (Biotin) Deficiency

15.3.7 Vitamin B12 (Cobalamin) Deficiency

15.3.8 Copper Deficiency

15.3.9 Tropical Sprue

15.3.10 Tropical Ataxic Neuropathy

15.4 Toxic Causes

15.4.1 NMDs Caused by Envenimation

15.4.1.1 Spider Bites

15.4.1.2 Scorpion Stings

15.4.1.3 Snake Bites

15.4.1.4 Marine Poisoning

15.4.1.5 Plant Sources and Other Animal Poisons

15.5 Other Acquired NMDs

15.5.1 Diabetes Mellitus

15.5.2 Immune-Mediated NMDs

15.5.2.1 Guillain–Barré Syndrome

15.5.2.2 CIDP

15.5.2.3 Myasthenia Gravis

15.5.3 Systemic Diseases

15.6 Hereditary NMDs

15.7 Idiopathic Neuropathies

Abbreviations

References

16 Headaches in Tropical Areas

16.1 Introduction

16.2 Epidemiological Aspects

16.3 Impact

16.4 Clinical Aspects

16.4.1 Migraine

16.4.2 Tension Headaches

16.4.3 Secondary Headache

16.4.3.1 Headache of Ophthalmological Origin

16.4.3.2 Headache in Intracranial Infection

16.4.3.3 Work-Related Headache

16.5 Conclusion

References

17 Neuropsychiatric Disorders and Addictions

17.1 Introduction

17.2 Psychiatry and Mental Health in SSA

17.2.1 Epidemiology in Mental Health in SSA

17.2.1.1 Prevalence of Mental Illness and Associated Factors

17.2.1.2 Women’s Mental Health

17.2.1.3 Childhood Mental Health

17.2.1.4 Mental Health in Prisons

17.2.1.5 Consequences of Mental-Health Diseases and Mental Quality of Life

17.2.2 Support for Mental Illness and Promotion of Mental Health

17.2.2.1 Obstacles

17.2.2.2 Solutions for More Effectively Dealing With Mental Health in SSA

17.3 Addictions in SSA

17.3.1 History and Generality of Addictions in SSA

17.3.1.1 The Local Production of Cannabis

17.3.1.2 Local Production of Heroin and Cocaine

17.3.2 Epidemiology of Addictions in SSA

17.3.2.1 Prevalence of Addictions in SSA

17.3.2.1.1 Prevalence of Addiction to Intravenous Drug Misuse in SSA

17.3.2.1.2 Drug Abuse and HIV

17.3.2.2 Specificity of the Addictions in Women in SSA

17.3.2.3 Prevalence of Addictions in Childhood and Adolescents in SSA

17.3.2.4 Factors Associated With Addictions in SSA

17.3.2.4.1 Factors Associated With Smoking in SSA

17.3.2.4.2 Factors Associated With Alcoholism in SSA

17.3.2.4.3 Factors Associated With Intravenous Drug Injection in SSA

17.3.2.4.4 Factors Associated With Addiction in Teenagers in SSA

17.3.2.4.5 Factors Associated With Addictions in Women SSA

17.3.2.5 The Consequences of Addictions in SSA

17.3.2.6 The Causes of Addiction in SSA

17.3.2.6.1 Causes of Alcoholism in SSA

17.3.2.6.2 Causes of the Tobacco Epidemic in Developing Countries

17.3.2.6.3 Causes of Illicit Drug Addiction in SSA

17.3.2.6.4 Causes of Trafficking of Drugs in SSA

17.3.3 Solutions to Addiction in SSA

17.3.3.1 Fighting Tobacco Control in SSA

17.3.3.2 The Fight Against Alcoholism

17.3.3.3 The Fight Against Drug Abuse and Trafficking of Psychotropic Drugs

17.4 Conclusion

References

Further Reading

18 Neurological Syndromes or Diseases Caused by Parasites in Tropical Areas

18.1 Introduction

18.2 Cysticercosis

18.3 American Trypanosomiasis

18.4 African Trypanosomiasis

18.5 Malaria

18.6 Schistosomiasis

18.7 Toxoplasmosis

18.8 Gnathostomiasis

18.9 Angiostrongyliasis

18.10 Nodding Syndrome and Onchocerciasis

18.11 Neurologic Infections by Free-Living Amebae

18.12 Future Directions

References

19 Bacterial Diseases of the Nervous System

19.1 Introduction

19.2 BM/Encephalitis/Cerebral Abscess (Mycobacteria Excluded)

19.2.1 Neonatal Meningitis

19.2.1.1 Epidemiology and Physiopathology

19.2.1.2 Diagnosis

19.2.1.3 Treatment

19.2.2 BM in Children and Adults

19.2.2.1 Epidemiology

19.2.2.1.1 Meningococcal Disease

19.2.2.1.2 Streptococcus pneumoniae

19.2.2.1.3 Other Pathogens

19.2.2.2 Pathophysiology

19.2.2.3 Clinical Features

19.2.2.4 Diagnosis

19.2.2.5 Treatment

19.2.2.6 Outcome

19.2.2.7 Prevention

19.2.2.7.1 Chemoprophylaxis

19.2.2.7.2 Vaccination

19.2.3 Cerebral Abscess

19.3 Mycobacterial Infections

19.3.1 TB of the CNS

19.3.1.1 Epidemiology

19.3.1.2 Pathophysiology

19.3.1.3 Clinical Features

19.3.1.4 Diagnosis

19.3.1.5 Treatment

19.3.1.6 Outcome

19.3.1.7 Prevention

19.3.1.7.1 Chemoprophylaxis

19.3.1.7.2 Vaccination: Bacille Calmette–Guérin

19.3.2 Leprosy

19.3.2.1 Epidemiology

19.3.2.2 Pathophysiology

19.3.2.3 Clinical Features

19.3.2.4 Diagnosis

19.3.2.5 Treatment

19.3.2.6 Outcome

19.3.2.7 Prevention

19.4 Other Bacterial Infections Involving the CNS

19.4.1 Neurosyphilis

19.4.1.1 Epidemiology

19.4.1.2 Physiopathology/Microbiology

19.4.1.3 Clinical Features

19.4.1.4 Diagnosis

19.4.1.5 Treatment

19.4.1.6 Outcome

19.4.1.7 Prevention136

19.4.2 Zoonotic BM

19.4.2.1 Leptospirosis, Brucellosis and Q Fever

19.4.2.1.1 Epidemiology

19.4.2.1.2 Physiopathology

19.4.2.1.3 Clinical Features

19.4.2.1.4 Diagnosis

19.4.2.1.5 Treatment

19.4.2.1.6 Outcome

19.4.2.1.7 Prevention

19.4.2.2 Rickettsiosis

19.4.2.3 Relapsing Fever

19.4.3 Mycoplasma pneumoniae

19.4.3.1 Physiopathology162,164 and Diagnosis

19.4.3.2 Treatment

19.4.4 Tetanus

19.4.4.1 Physiopathology

19.4.4.2 Diagnosis

19.4.4.3 Mortality

19.4.4.4 Outcome in Survivors

19.4.4.5 Treatment

19.4.4.6 Prevention

References

20 Viral Diseases

20.1 Introduction

20.2 Herpes Simplex 1 and 2

20.2.1 Epidemiology

20.2.2 CNS Diseases Caused by HSV

20.2.3 Pathogenesis

20.2.4 Diagnosis

20.2.5 Prevention and Treatment

20.3 Varicella Zoster Virus

20.3.1 Epidemiology

20.3.2 Pathogenesis

20.3.3 Diagnosis

20.3.4 Treatment

20.3.5 Prevention

20.4 Cytomegalovirus

20.4.1 Epidemiology

20.4.2 Pathogenesis

20.4.3 Diagnosis

20.4.4 Treatment and Prevention

20.5 Epstein–Barr Virus

20.5.1 Epidemiology

20.5.2 Pathogenesis

20.5.3 Diagnosis

20.5.4 Treatment and Prevention

20.6 Human Herpes Virus 6

20.7 Enterovirus

20.8 Poliomyelitis

20.8.1 Epidemiology

20.8.2 Pathogenesis

20.8.3 Diagnosis

20.8.4 Treatment and Prevention

20.9 Non-polio Enteroviruses

20.9.1 Epidemiology and Clinical Features

20.9.2 Diagnosis

20.9.3 Treatment and Prevention

20.10 Paramyxoviruses (Measles, Mumps, and Nipah Viruses)

20.10.1 Measles

20.10.1.1 Epidemiology

20.10.1.2 Diagnosis

20.10.1.3 Prevention and Treatment

20.10.2 Mumps

20.10.2.1 Epidemiology

20.10.2.2 Pathogenesis

20.10.2.3 Diagnosis

20.10.2.4 Prevention and Treatment

20.10.3 Nipah Virus

20.10.3.1 Epidemiology

20.10.3.2 Pathogenesis and Pathology

20.10.3.3 Diagnosis

20.10.3.4 Prevention and Treatment

20.11 Retrovirus

20.11.1 Human T–Lymphotropic Virus

20.11.1.1 Epidemiology

20.11.1.2 Pathogenesis

20.11.1.3 Diagnosis

20.11.1.4 Prevention and Treatment

20.11.2 Human Immunodeficiency Virus

20.11.2.1 Epidemiology

20.11.2.2 Pathogenesis

20.11.2.3 Diagnosis

20.11.2.4 Prevention and Treatment

20.12 Polyomavirus and Progressive Multifocal Leucoencephalopathy

20.12.1 Epidemiology

20.12.2 Pathogenesis

20.12.3 Diagnosis

20.12.4 Prevention and Treatment

20.13 Rhabdoviridae/Lyssavirus

20.13.1 Epidemiology

20.13.2 Pathogenesis

20.13.3 Diagnosis

20.13.4 Prevention and Treatment

20.14 Arboviruses

20.14.1 Bunyaviridae Family

20.14.2 Flaviviridae Family, Genus Flavivirus

20.14.2.1 Epidemiology

20.14.2.2 Clinical Features

20.14.2.3 Diagnosis

20.14.2.4 Prevention and Treatment

20.15 Togaviridae/Rubivirus

20.15.1 Epidemiology

20.15.2 Pathogenesis

20.15.3 Diagnosis

20.15.4 Prevention

20.16 Poxviruses/Smallpox and Vaccinia

20.16.1 Epidemiology

20.16.2 Prevention and Safety of the Vaccine

References

Further Reading

21 Other Diseases: Traumatic Brain Injuries, Tumors, and Multiple Sclerosis

21.1 Traumatic Brain Injuries

21.1.1 Frequency

21.1.2 Distribution by Age and Sex

21.1.3 The Circumstances of Occurrence

21.1.4 Morbidity and Mortality

21.2 Tumors

21.2.1 PBT Risk Factors

21.2.1.1 Endogenous Factors

21.2.1.1.1 Age and Sex

21.2.1.1.2 Genetic Factors

21.2.1.1.3 Allergic Conditions

21.2.1.1.4 Anthropometric Factors

21.2.1.2 Exogenous Factors

21.2.1.2.1 Ionizing Radiations

21.2.1.2.2 Magnetic Fields

21.2.1.2.3 Viral Infections

21.2.1.2.4 Nitrates

21.2.2 Frequency

21.2.3 Breakdown by Location and Nature of Tumors

21.3 Multiple Sclerosis

References

Glossary

Index

Back Cover

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