Handbook of Oral Pathology and Oral Medicine

Handbook of Oral Pathology and Oral Medicine
Автор книги: id книги: 2131148     Оценка: 0.0     Голосов: 0     Отзывы, комментарии: 0 8935,13 руб.     (87,31$) Читать книгу Купить и скачать книгу Электронная книга Жанр: Медицина Правообладатель и/или издательство: John Wiley & Sons Limited Дата добавления в каталог КнигаЛит: ISBN: 9781119781158 Скачать фрагмент в формате   fb2   fb2.zip Возрастное ограничение: 0+ Оглавление Отрывок из книги

Реклама. ООО «ЛитРес», ИНН: 7719571260.

Описание книги

Handbook of Oral Pathology and Oral Medicine Discover a concise overview of the most common oral diseases in a reader-friendly book Handbook of Oral Pathology and Oral Medicine delivers a succinct overview of a range of oral diseases. The book contains up-to-date evidence-based information organized by clinical topic and supported by over 300 clinical, radiological, and microscopic images. Each chapter includes topics following universally respected curricula of oral pathology and oral medicine. Divided into seven parts, it covers core topics such as pathology of teeth, pulp, and supporting structures, pathology of jawbones, pathology of the oral mucosa, pathology of the salivary glands, clinical presentation of mucosal disease, orofacial pain, and miscellaneous topics of clinical relevance. Written for undergraduate dental students, dental hygienists and oral health therapists, Handbook of Oral Pathology and Oral Medicine is an ideal quick reference and is also useful to dental educators and practitioners.

Оглавление

S. R. Prabhu. Handbook of Oral Pathology and Oral Medicine

Table of Contents

List of Tables

List of Illustrations

Guide

Pages

Handbook of Oral Pathology and Oral Medicine

Foreword

Preface

Acknowledgements

About the Companion Website

Nomenclature Used in The Study of Human Disease

Standard Abbreviations for Prescribers

1 Disorders of Tooth Development and Eruption. CHAPTER MENU

1.1 Anodontia, Hypodontia and Oligodontia. 1.1.1 Definition/Description

1.1.2 Frequency

1.1.3 Aetiology/Risk Factors

1.1.4 Clinical Features

1.1.5 Radiographical Features

1.1.6 Diagnosis

1.1.7 Management

1.2 Hyperdontia (Supernumerary Teeth) 1.2.1 Definition/Description

1.2.2 Frequency

1.2.3 Aetiology/Risk Factors

1.2.4 Clinical Features

1.2.5 Radiographical Features

1.2.6 Diagnosis

1.2.7 Management

1.3 Microdontia and Macrodontia. 1.3.1 Definition/Description

1.3.2 Frequency

1.3.3 Aetiology/Risk Factors

1.3.4 Clinical Features

1.3.5 Diagnosis

1.3.6 Management

1.4 Gemination, Fusion and Concrescence. 1.4.1 Definition/Description

1.4.2 Frequency

1.4.3 Aetiology/Risk Factors

1.4.4 Clinical Features

1.4.5 Radiographical Features

1.4.6 Diagnosis

1.4.7 Management

1.5 Taurodontism and Dilaceration. 1.5.1 Definition/Description

1.5.2 Frequency

1.5.3 Aetiology/Risk Factors

1.5.4 Clinical Features

1.5.5 Radiographical Features

1.5.6 Management

1.6 Amelogenesis Imperfecta. 1.6.1 Definition/Description

1.6.2 Incidence/Prevalence

1.6.3 Aetiology/Risk Factors

1.6.4 Clinical/Radiographical Features

1.6.5 Differential diagnosis

1.6.6 Diagnosis

1.6.7 Management

1.7 Dentinogenesis Imperfecta. 1.7.1 Definition/Description

1.7.2 Frequency

1.7.3 Aetiology/Risk Factors

1.7.4 Clinical Features

1.7.5 Radiographical features

1.7.6 Differential Diagnosis

1.7.7 Diagnosis

1.7.8 Management

1.8 Dentinal Dysplasia (Dentin Dysplasia) 1.8.1 Definition/Description

1.8.2 Frequency

1.8.3 Aetiology/Risk Factors

1.8.4 Clinical Features

1.8.5 Radiographical features

1.8.6 Differential Diagnosis

1.8.7 Diagnosis

1.8.8 Management

1.9 Regional Odontodysplasia (Ghost Teeth) 1.9.1 Definition/Description

1.9.2 Frequency

1.9.3 Aetiology/Risk Factors

1.9.4 Clinical Features

1.9.5 Radiographical features

1.9.6 Differential Diagnosis

1.9.7 Diagnosis

1.9.8 Management

1.10 Delayed Tooth Eruption. 1.10.1 Definition/Description

1.10.2 Frequency

1.10.3 Aetiology/Risk Factors

1.10.4 Clinical and Radiographical Features

1.10.5 Diagnosis

1.10.6 Management

1.11 Tooth Impaction (Impacted Teeth) 1.11.1 Definition/Description

1.11.2 Frequency

1.11.3 Aetiology

1.11.4 Clinical Features

1.11.5 Radiographical Features

1.11.6 Diagnosis

1.11.7 Management

1.12 Dens Invaginatus and Dens Evaginatus. 1.12.1 Definition/Description

1.12.2 Frequency

1.12.3 Aetiology/Risk Factors

1.12.4 Clinical Features

1.12.5 Radiographical features

1.12.6 Diagnosis

1.12.7 Management

1.13 Fluorosis (Mottled Enamel) 1.13.1 Definition/Description

1.13.2 Frequency

1.13.3 Aetiology/Risk Factors

1.13.4 Clinical Features

1.13.5 Differential Diagnosis

1.13.6 Diagnosis

1.13.7 Management

1.14 Tetracycline‐Induced Discoloration of Teeth: Key Features

1.15 Enamel Pearl: Key Features

1.16 Talon Cusp: Key Features

1.17 Hutchinson's Incisors and Mulberry Molars: Key Features

1.18 Tooth Ankylosis: Key Features

1.19 Supernumerary Roots: Key Features

Recommended Reading

2 Dental caries. CHAPTER MENU

2.1 Definition/Description

2.2 Frequency

2.3 Aetiology/Risk Factors/Pathogenesis

2.4 Classification of Caries

2.5 Clinical Features

2.5.1 Primary Caries

2.5.2 Secondary Caries (Recurrent Caries)

2.5.3 Arrested Caries

2.5.4 Rampant Caries

2.5.5 Early Childhood Caries

2.5.6 Methamphetamine‐Induced Caries

2.5.7 Radiation Caries

2.6 Differential Diagnosis

2.7 Diagnosis

2.8 Microsopic Features. 2.8.1 Enamel Caries

2.8.2 Dentinal Caries

2.9 Management

2.10 Prevention

Recommended Reading

3 Diseases of the Pulp and Apical Periodontal Tissues. CHAPTER MENU

3.1 Classification of Diseases of the Pulp and Apical Periodontal Tissues

3.2 Pulpitis. 3.2.1 Definition/Description

3.2.2 Frequency

3.2.3 Aetiology/Risk Factors

3.2.4 Clinical and Radiographical Features

3.2.5 Microscopic Features

3.2.6 Differential Diagnosis

3.2.7 Diagnosis

3.2.8 Management. 3.2.8.1 Reversible Pulpitis

3.2.8.2 Irreversible Pulpitis

3.2.8.3 Chronic Hyperplastic Pulpitis

3.3 Apical Periodontitis and Periapical Granuloma. 3.3.1 Definition/Description

3.3.2 Frequency

3.3.3 Aetiology/Risk Factors

3.3.4 Clinical Features

3.3.5 Radiographical Features

3.3.6 Microscopic Features

3.3.7 Differential Diagnosis

3.3.8 Diagnosis

3.3.9 Management

3.4 Apical Abscess (Dentoalveolar Abscess) 3.4.1 Definition/Description

3.4.2 Frequency

3.4.3 Aetiology/Risk Factors

3.4.4 Clinical and Radiographical Features

3.4.5 Differential Diagnosis

3.4.6 Diagnosis

3.4.7 Management

3.5 Condensing Osteitis. 3.5.1 Definition/Description

3.5.2 Frequency

3.5.3 Aetiology

3.5.4 Clinical Features

3.5.5 Radiographical Features

3.5.6 Microscopic Features

3.5.7 Differential Diagnosis

3.5.8 Diagnosis

3.5.9 Management

Recommended Reading

4 Tooth Wear, Pathological Resorption of Teeth, Hypercementosis and Cracked Tooth Syndrome. CHAPTER MENU

4.1 Tooth wear: Attrition, Abrasion, Erosion, and Abfraction. 4.1.1 Definition/Description

4.1.2 Frequency

4.1.3 Aetiology/Risk Factors

4.1.4 Clinical Features

4.1.5 Differential diagnosis

4.1.6 Diagnosis

4.1.7 Management

4.1.8 Prognosis

4.2 Pathological Resorption of Teeth. 4.2.1 Definition/Description

4.2.2 Frequency

4.2.3 Aetiology/Risk Factors

4.2.4 Clinical Features

4.2.5 Radiographical features

4.2.6 Microscopic Features

4.2.7 Differential diagnosis

4.2.8 Diagnosis

4.2.9 Management

4.2.10 Prognosis

4.3 Hypercementosis. 4.3.1 Definition/Description

4.3.2 Frequency

4.3.3 Aetiology/Risk Factors

4.3.4 Clinical Features

4.3.5 Radiographical features

4.3.6 Microscopic Features

4.3.7 Differential Diagnosis

4.3.8 Management

4.4 Cracked Tooth Syndrome. 4.4.1 Definition/Description

4.4.2 Frequency

4.4.3 Aetiology/Risk factors

4.4.4 Clinical Features

4.4.5 Differential Diagnosis

4.4.6 Diagnosis

4.4.7 Management

4.4.8 Prognosis

Recommended Reading

5 Gingival and Periodontal Diseases. CHAPTER MENU

5.1 Classification of Gingival and Periodontal Diseases

5.2 Chronic Gingivitis. 5.2.1 Definition/Description

5.2.2 Frequency

5.2.3 Aetiology/Risk Factors

5.2.4 Clinical Features

5.2.5 Microscopic Features

5.2.6 Differential Diagnosis

5.2.7 Diagnosis

5.2.8 Management

5.2.9 Prognosis

5.3 Necrotizing Periodontal Diseases. 5.3.1 Definition/Description

5.3.2 Frequency

5.3.3 Aetiology/Risk Factors

5.3.4 Clinical Features

5.3.5 Microscopic Features

5.3.6 Differential Diagnosis

5.3.7 Diagnosis

5.3.8 Management

5.3.9 Prognosis

5.4 Plasma Cell Gingivitis. 5.4.1 Definition/Description

5.4.2 Frequency

5.4.3 Aetiology/Risk Factors

5.4.4 Clinical Features

5.4.5 Microscopic Features

5.4.6 Differential Diagnosis

5.4.7 Diagnosis

5.4.8 Management

5.4.9 Prognosis

5.5 Foreign Body Gingivitis. 5.5.1 Definition/Description

5.5.2 Frequency

5.5.3 Aetiology/Risk Factors

5.5.4 Clinical Features

5.5.5 Microscopic Features

5.5.6 Differential Diagnosis

5.5.7 Diagnosis

5.5.8 Management

5.5.9 Prognosis

5.6 Desquamative Gingivitis. 5.6.1 Definition/Description

5.6.2 Frequency

5.6.3 Aetiology/Risk Factors

5.6.4 Clinical Features

5.6.5 Microscopic Features

5.6.6 Differential Diagnosis

5.6.7 Diagnosis

5.6.8 Management

5.6.9 Prognosis

5.7 Chronic Periodontitis. 5.7.1 Definition/Description

5.7.2 Frequency

5.7.3 Aetiology/Risk Factors

5.7.4 Clinical Features

5.7.5 Radiographical features

5.7.6 Microscopic Features

5.7.7 Differential Diagnosis

5.7.8 Diagnosis

5.7.9 Management

5.7.10 Prognosis

5.7.11 Complications of Chronic Periodontitis

5.8 Aggressive Periodontitis. 5.8.1 Definition/Description

5.8.2 Frequency

5.8.3 Aetiology/Risk Factors

5.8.4 Clinical and Radiographical Features

5.8.5 Microscopic Features

5.8.6 Differential Diagnosis

5.8.7 Diagnosis

5.8.8 Management

5.8.9 Prognosis

5.9 Fibrous Epulis (Peripheral Fibroma) 5.9.1 Definition/Description

5.9.2 Frequency

5.9.3 Aetiology/Risk factors

5.9.4 Clinical Features

5.9.5 Microscopic Features

5.9.6 Differential Diagnosis

5.9.7 Diagnosis

5.9.8 Management

5.9.9 Prognosis

5.10 Peripheral Ossifying/Cementifying Fibroma. 5.10.1 Definition/Description

5.10.2 Frequency

5.10.3 Aetiology/Risk Factors

5.10.4 Clinical Features

5.10.5 Microscopic Features

5.10.6 Differential Diagnosis

5.10.7 Diagnosis

5.10.8 Management

5.10.9 Prognosis

5.11 Peripheral Giant Cell Granuloma (Giant Cell Epulis) 5.11.1 Definition/Description

5.11.2 Frequency

5.11.3 Aetiology/Risk Factors

5.11.4 Clinical Features

5.11.5 Microscopic Features

5.11.6 Differential Diagnosis

5.11.7 Diagnosis

5.11.8 Management

5.11.9 Prognosis

5.12 Angiogranuloma (Pyogenic granuloma/pregnancy epulis) 5.12.1 Definition/Description

5.12.2 Frequency

5.12.3 Aetiology/Risk Factors

5.12.4 Clinical Features

5.12.5 Microscopic Features

5.12.6 Differential Diagnosis

5.12.7 Diagnosis

5.12.8 Management

5.12.9 Prognosis

5.13 Inflammatory Gingival Hyperplasia (Inflammatory Gingival Enlargement) 5.13.1 Definition/Description

5.13.2 Frequency

5.13.3 Aetiology

5.13.4 Clinical Features

5.13.5 Microscopic Features

5.13.6 Differential Diagnosis

5.13.7 Diagnosis

5.13.8 Management

5.13.9 Prognosis

5.14 Generalized Gingival Hyperplasia in Pregnancy. 5.14.1 Definition/Description

5.14.2 Frequency

5.14.3 Aetiology/Risk Factors

5.14.4 Clinical Features

5.14.5 Microscopic Features

5.14.6 Differential Diagnosis

5.14.7 Diagnosis

5.14.8 Management

5.14.9 Prognosis

5.15 Drug‐Induced Gingival Hyperplasia. 5.15.1 Definition/Description

5.15.2 Frequency

5.15.3 Aetiology/Risk Factors

5.15.4 Clinical Features

5.15.5 Microscopic Features

5.15.6 Differential Diagnosis

5.15.7 Diagnosis

5.15.8 Management

5.15.9 Prognosis

5.16 Familial Gingival Hyperplasia. 5.16.1 Definition/Description

5.16.2 Frequency

5.16.3 Aetiology/Risk Factors

5.16.4 Clinical Features

5.16.5 Microscopic Features

5.16.6 Differential Diagnosis

5.16.7 Diagnosis

5.16.8 Management

5.16.9 Prognosis

5.17 Gingival and Periodontal Abscesses. 5.17.1 Definition/Description

5.17.2 Frequency

5.17.3 Aetiology/Risk Factors

5.17.4 Clinical Features

5.17.5 Microscopic Features

5.17.6 Differential Diagnosis

5.17.7 Diagnosis

5.17.8 Management. 5.17.8.1 Gingival Abscess

5.17.8.2 Periodontal Abscess

5.17.9 Prognosis

5.18 Pericoronitis/Pericoronal Abscess. 5.18.1 Definition/Description

5.18.2 Frequency

5.18.3 Aetiology/Risk Factors. 5.18.3.1 Aetiology

5.18.3.2 Risk Factors

5.18.3.3 Microbial Association

5.18.3.4 Clinical Features

5.18.4 Microscopic Features

5.18.5 Differential Diagnosis

5.18.6 Diagnosis

5.18.7 Management

5.18.8 Prognosis

5.19 Gingival Enlargement in Granulomatosis with Polyangiitis (Wegener's granulomatosis) 5.19.1 Definition/Description

5.19.2 Frequency

5.19.3 Aetiology/Risk Factors

5.19.4 Clinical Features

5.19.5 Microscopic Features

5.19.6 Differential Diagnosis

5.19.7 Diagnosis

5.19.8 Management

5.19.9 Prognosis

5.20 Gingival Enlargement in Leukaemia. 5.20.1 Definition/Description

5.20.2 Frequency

5.20.3 Aetiology/Risk Factors

5.20.4 Clinical Features

5.20.5 Microscopic Features

5.20.6 Differential Diagnosis

5.20.7 Diagnosis

5.20.8 Management

5.20.9 Prognosis

5.21 Gingival Enlargement in Ascorbic Acid Deficiency. 5.21.1 Definition

5.21.2 Frequency

5.21.3 Aetiology/Risk Factors

5.21.4 Clinical Features

5.21.5 Microscopic Features

5.21.6 Differential Diagnosis

5.21.7 Diagnosis

5.21.8 Management

5.21.9 Prognosis

Recommended Reading

6 Infections and Necrosis of the Jaw. CHAPTER MENU

6.1 Acute Suppurative Osteomyelitis. 6.1.1 Definition/Description

6.1.2 Frequency

6.1.3 Aetiology/Risk Factors

6.1.4 Clinical Features

6.1.5 Radiographical Features

6.1.6 Microscopic Features

6.1.7 Differential Diagnosis

6.1.8 Diagnosis

6.1.9 Management

6.1.10 Prognosis

6.2 Chronic Suppurative Osteomyelitis. 6.2.1 Definition/Description

6.2.2 Frequency

6.2.3 Aetiology/Risk Factors

6.2.4 Clinical Features

6.2.5 Radiographical Features

6.2.6 Microscopic Features

6.2.7 Differential Diagnosis

6.2.8 Diagnosis

6.2.9 Management

6.2.10 Prognosis

6.3 Sclerosing Osteomyelitis. 6.3.1 Definition/Description

6.3.2 Frequency

6.3.3 Aetiology/Risk Factors

6.3.4 Clinical Features

6.3.5 Radiographical Features

6.3.6 Microscopic Features

6.3.7 Differential Diagnosis

6.3.8 Diagnosis

6.3.9 Management

6.3.10 Prognosis

6.4 Proliferative Periostitis (Garre's Osteomyelitis) 6.4.1 Definition/Description

6.4.2 Frequency

6.4.3 Aetiology/Risk Factors

6.4.4 Clinical Features

6.4.5 Radiographical Features

6.4.6 Microscopic Features

6.4.7 Differential Diagnosis

6.4.8 Diagnosis

6.4.9 Management

6.4.10 Prognosis

6.5 Actinomycosis of the Jaw. 6.5.1 Definition

6.5.2 Frequency

6.5.3 Aetiology/Risk Factors

6.5.4 Clinical Features

6.5.5 Microscopic Features

6.5.6 Differential Diagnosis

6.5.7 Diagnosis

6.5.8 Management

6.5.9 Prognosis

6.6 Cervicofacial Cellulitis (Cervicofacial Fascial Space Infection) 6.6.1 Definition

6.6.2 Frequency

6.6.3 Aetiology/Risk Factors

6.6.4 Clinical Features

6.6.5 Diagnosis

6.6.6 Management

6.6.7 Prognosis

6.7 Osteoradionecrosis of the Jaw. 6.7.1 Definition/Description

6.7.2 Frequency

6.7.3 Aetiology/Risk Factors

6.7.4 Clinical Features

6.7.5 Radiographical Features

6.7.6 Microscopic Features

6.7.7 Differential Diagnosis

6.7.8 Diagnosis

6.7.9 Management

6.7.10 Prognosis

6.8 Medication‐Related Osteonecrosis of the Jaw. 6.8.1 Definition/Description

6.8.2 Frequency

6.8.3 Aetiology/Risk Factors

6.8.4 Clinical Features

6.8.5 Radiographical Features

6.8.6 Microscopic Features

6.8.7 Differential Diagnosis

6.8.8 Diagnosis

6.8.9 Management

Prognosis

Recommended Reading

7 Cysts of the Jaw. CHAPTER MENU

7.1 Radicular, Lateral Radicular, and Residual Radicular Cysts. 7.1.1 Definition/Description

7.1.2 Frequency

7.1.3 Aetiology/Risk Factors

7.1.4 Clinical/Radiographical Features

7.1.5 Microscopic Features

7.1.6 Differential Diagnosis

7.1.7 Diagnosis

7.1.8 Management

7.1.9 Prognosis

7.2 Dentigerous Cyst. 7.2.1 Definition/Description

7.2.2 Frequency

7.2.3 Aetiology/Risk Factors

7.2.4 Clinical Features

7.2.5 Radiographical Findings

7.2.6 Microscopic Features

7.2.7 Differential Diagnosis

7.2.8 Diagnosis

7.2.9 Management

7.2.10 Prognosis

7.3 Eruption Cyst. 7.3.1 Definition

7.3.2 Frequency

7.3.3 Aetiology/Risk Factors

7.3.4 Clinical Features

7.3.5 Microscopic Features

7.3.6 Differential Diagnosis

7.3.7 Diagnosis

7.3.8 Management

7.3.9 Prognosis

7.4 Odontogenic Keratocyst (Keratocystic Odontogenic Tumour) 7.4.1 Definition

7.4.2 Frequency

7.4.3 Aetiology/Risk Factors

7.4.4 Clinical Features

7.4.5 Radiographical Features

7.4.6 Microscopic Features

7.4.7 Other Features

7.4.8 Differential Diagnosis

7.4.9 Diagnosis

7.4.10 Management

7.4.11 Prognosis

7.5 Lateral Periodontal Cyst. 7.5.1 Definition/Description

7.5.2 Frequency

7.5.3 Origin/Aetiology/Risk Factors

7.5.4 Clinical Features

7.5.5 Radiographical Features

7.5.6 Microscopic Features

7.5.7 Differential Diagnosis

7.5.8 Diagnosis

7.5.9 Prognosis

7.6 Calcifying Odontogenic Cyst. 7.6.1 Definition/Description

7.6.2 Frequency

7.6.3 Origin/Aetiology/Risk Factors

7.6.4 Clinical Features

7.6.5 Radiographical Features

7.6.6 Microscopic Features

7.6.7 Differential Diagnosis

7.6.8 Diagnosis

7.6.9 Management

7.6.10 Prognosis

7.7 Orthokeratinized Odontogenic Cyst: Key Features

7.8 Glandular Odontogenic Cyst: Key Features

7.9 Nasopalatine Duct Cyst (Incisive Canal Cyst) 7.9.1 Definition/Description

7.9.2 Frequency

7.9.3 Aetiology/Risk Factors

7.9.4 Clinical Features

7.9.5 Radiographical Features

7.9.6 Microscopic Features

7.9.7 Differential Diagnosis

7.9.8 Diagnosis

7.9.9 Management

7.9.10 Prognosis

7.10 Pseudocysts of the Jaw: Solitary Bone Cyst, Aneurysmal Bone Cyst and Stafne's bone Cyst

7.10.1 Definition/Description

7.10.2 Frequency

7.10.3 Aetiology

7.10.4 Clinical Features

7.10.5 Microscopic Features

7.10.6 Differential Diagnosis

7.10.7 Diagnosis

7.10.8 Management

7.10.9 Prognosis

7.11 Nasolabial Cyst: Key Features

Recommended Reading

8 Odontogenic Tumours. CHAPTER MENU

8.1 World Health Organization Classification of Odontogenic Tumours (2017)

8.2 Ameloblastoma. 8.2.1 Definition/Description

8.2.2 Frequency

8.2.3 Aetiology/Risk Factors

8.2.4 Clinical Features

8.2.5 Radiographical Features

8.2.6 Microscopic Features

8.2.7 Diagnosis

8.2.8 Differential Diagnosis

8.2.9 Management

8.2.10 Prognosis

8.3 Unicystic Ameloblastoma. 8.3.1 Definition/Description

8.3.2 Frequency

8.3.3 Aetiology/Risk Factors

8.3.4 Clinical Signs and Symptoms

8.3.5 Radiographical Features

8.3.6 Microscopic Features

8.3.7 Differential Diagnosis

8.3.8 Diagnosis

8.3.9 Management

8.3.10 Prognosis

8.4 Squamous Odontogenic Tumour. 8.4.1 Definition/Description

8.4.2 Frequency

8.4.3 Aetiology/Risk Factors

8.4.4 Clinical features

8.4.5 Radiographical Features

8.4.6 Microscopic Features

8.4.7 Differential Diagnosis

8.4.8 Diagnosis

8.4.9 Management

8.4.10 Prognosis

8.5 Calcifying Epithelial Odontogenic Tumour (Pindborg Tumour) 8.5.1 Definition/Description

8.5.2 Frequency

8.5.3 Aetiology/Risk Factors

8.5.4 Clinical Features

8.5.5 Radiographical Features

8.5.6 Microscopic Features

8.5.7 Differential Diagnosis

8.5.8 Diagnosis

8.5.9 Management

8.5.10 Prognosis

8.6 Adenomatoid Odontogenic Tumour. 8.6.1 Definition/Description

8.6.2 Frequency

8.6.3 Aetiology/Risk Factors

8.6.4 Clinical features

8.6.5 Radiographical Features

8.6.6 Microscopic Features

8.6.7 Differential Diagnosis

8.6.8 Diagnosis

8.6.9 Management

8.6.10 Prognosis

8.7 Ameloblastic Fibroma. 8.7.1 Definition/Description

8.7.2 Frequency

8.7.3 Aetiology/Risk Factors

8.7.4 Clinical features

8.7.5 Radiographical Features

8.7.6 Microscopic Features

8.7.7 Differential Diagnosis

8.7.8 Diagnosis

8.7.9 Management

8.7.10 Prognosis

8.8 Ameloblastic Fibrodentinoma and Ameloblastic Fibro‐Odontome. 8.8.1 Definition/Description

8.8.2 Frequency

8.8.3 Aetiology/Risk Factors

8.8.4 Clinical features

8.8.5 Radiographical Features

8.8.6 Microscopic Features

8.8.7 Differential Diagnosis

8.8.8 Diagnosis

8.8.9 Management

8.8.10 Prognosis

8.9 Odontome (Odontoma) 8.9.1 Definition/Description

8.9.2 Frequency

8.9.3 Aetiology/Risk Factors

8.9.4 Clinical Features

8.9.5 Radiographical Features

8.9.6 Microscopic Features

8.9.7 Differential Diagnosis

8.9.8 Diagnosis

8.9.9 Management

8.9.10 Prognosis

8.10 Dentinogenic Ghost Cell Tumour. 8.10.1 Definition/Description

8.10.2 Frequency

8.10.3 Aetiology/Risk Factors

8.10.4 Clinical features

8.10.5 Radiographical Features

8.10.6 Microscopic Features

8.10.7 Differential Diagnosis

8.10.8 Diagnosis

8.10.9 Management

8.10.10 Prognosis

8.11 Odontogenic Myxoma. 8.11.1 Definition/Description

8.11.2 Frequency

8.11.3 Aetiology/Risk Factors

8.11.4 Clinical features

8.11.5 Radiographical Features

8.11.6 Microscopic Features

8.11.7 Differential Diagnosis

8.11.8 Diagnosis

8.11.9 Management

8.11.10 Prognosis

8.12 Odontogenic Fibroma (Central Odontogenic Fibroma) 8.12.1 Definition/description

8.12.2 Aetiology/Risk factors

8.12.3 Frequency

8.12.4 Clinical Features

8.12.5 Radiographical Features

8.12.6 Microscopic Features

8.12.7 Differential Diagnosis

8.12.8 Diagnosis

8.12.9 Management

8.13 Cementoblastoma. 8.13.1 Definition/Description

8.13.2 Frequency

8.13.3 Aetiology/Risk Factors

8.13.4 Clinical Features

8.13.5 Radiographical Features

8.13.6 Microscopic Features

8.13.7 Differential Diagnosis

8.13.8 Diagnosis

8.13.9 Management

8.13.10 Prognosis

Recommended Reading

9 Non‐odontogenic Benign and Malignant Tumours of the Jaw. CHAPTER MENU

9.1 Osteoma. 9.1.1 Definition/Description

9.1.2 Frequency

9.1.3 Aetiology

9.1.4 Clinical Features

9.1.5 Radiographical Features

9.1.6 Microscopic Features

9.1.7 Differential Diagnosis

9.1.8 Diagnosis

9.1.9 Management

9.2 Multiple Osteomas in Gardner's Syndrome. 9.2.1 Definition

9.2.2 Frequency

9.2.3 Aetiology

9.2.4 Clinical Features

9.2.5 Radiographical Features

9.2.6 Microscopic Features

9.2.7 Differential Diagnosis

9.2.8 Diagnosis

9.2.9 Management

9.2.10 Prognosis

9.3 Central Haemangioma (Intraosseous Haemangioma) 9.3.1 Definition/Description

9.3.2 Frequency

9.3.3 Aetiology

9.3.4 Clinical Features

9.3.5 Radiographical Features

9.3.6 Microscopic Features

9.3.7 Differential Diagnosis

9.3.8 Diagnosis

9.3.9 Management

9.3.10 Prognosis

9.4 Melanotic Neuroectodermal Tumour of Infancy. 9.4.1 Definition/Description

9.4.2 Frequency

9.4.3 Aetiology

9.4.4 Clinical Features

9.4.5 Radiographical Features

9.4.6 Microscopic Features

9.4.7 Differential Diagnosis

9.4.8 Diagnosis

9.4.9 Management

9.4.10 Prognosis

9.5 Osteosarcoma. 9.5.1 Definition/Description

9.5.2 Frequency

9.5.3 Aetiology/Predisposing Factors

9.5.4 Clinical Features

9.5.5 Radiographical Features

9.5.6 Microscopic Features

9.5.7 Differential Diagnosis

9.5.8 Diagnosis

9.5.9 Management

9.5.10 Prognosis

9.6 Chondrosarcoma: Key Features

9.6.1 Prognosis

9.7 Ewing's Sarcoma. 9.7.1 Definition/Description

9.7.2 Frequency

9.7.3 Aetiology/Risk Factors

9.7.4 Clinical Features

9.7.5 Radiographical Features

9.7.6 Microscopic Features

9.7.7 Differential Diagnosis

9.7.8 Diagnosis

9.7.9 Management

9.7.10 Prognosis

9.8 Myeloma (Multiple Myeloma) 9.8.1 Definition/Description

9.8.2 Frequency

9.8.3 Aetiology/Risk Factors

9.8.4 Clinical Features

9.8.5 Radiographical Features

9.8.6 Microscopic Features

9.8.7 Differential Diagnosis

9.8.8 Diagnosis

9.8.9 Management

9.8.10 Prognosis

9.9 Solitary Plasmacytoma. 9.9.1 Definition/Description

9.9.2 Frequency

9.9.3 Aetiology/Risk Factors

9.9.4 Clinical Features

9.9.5 Radiographical Features

9.9.6 Microscopic Features

9.9.7 Differential Diagnosis

9.9.8 Diagnosis

9.9.9 Management

9.9.10 Prognosis

9.10 Burkitt's Lymphoma. 9.10.1 Definition/Description

9.10.2 Frequency

9.10.3 Aetiology/Risk Factors

9.10.4 Clinical Features

9.10.5 Radiographical Features

9.10.6 Microscopic Features

9.10.7 Differential Diagnosis

9.10.8 Management/Prognosis

Recommended Reading

10 Fibro‐Osseous and Related Lesions of the Jaw. CHAPTER MENU

10.1 Ossifying Fibroma/Cemento‐Ossifying Fibroma. 10.1.1 Definition/Description

10.1.2 Frequency

10.1.3 Origin/Aetiology

10.1.4 Clinical/Radiographical Features

10.1.5 Microscopic Features

10.1.6 Differential Diagnosis

10.1.7 Diagnosis

10.1.8 Management

10.2 Cemento‐Osseous Dysplasias. 10.2.1 Definition/Description

10.2.2 Frequency

10.2.3 Aetiology

10.2.4 Clinical/Radiographical Features

10.2.5 Microscopic Features

10.2.6 Differential Diagnosis

10.2.7 Diagnosis

10.2.8 Management

10.2.9 Prognosis

10.3 Familial Gigantiform Cementoma: Key Features

10.4 Central Giant Cell Granuloma. 10.4.1 Definition/Description

10.4.2 Frequency

10.4.3 Origin/Aetiology

10.4.4 Clinical Features

10.4.5 Radiographical Features

10.4.6 Microscopic Features

10.4.7 Differential Diagnosis

10.4.8 Diagnosis

10.4.9 Management

10.4.10 Prognosis

Recommended Reading

11 Genetic, Metabolic, and Other Non‐neoplastic Bone Diseases. CHAPTER MENU

11.1 Osteogenesis Imperfecta. 11.1.1 Definition/Description

11.1.2 Frequency

11.1.3 Aetiology/Risk Factors

11.1.4 Clinical Features

11.1.5 Radiographical Features

11.1.6 Diagnosis

11.1.7 Management

11.2 Cleidocranial Dysplasia. 11.2.1 Definition/Description

11.2.2 Frequency

11.2.3 Aetiology

11.2.4 Clinical Features

11.2.5 Radiographical Features

11.2.6 Differential Diagnosis

11.2.7 Diagnosis

11.2.8 Management

11.3 Cherubism. 11.3.1 Definition/Description

11.3.2 Frequency

11.3.3 Aetiology

11.3.4 Clinical Features

11.3.5 Radiographical Findings

11.3.6 Microscopic Features

11.3.7 Differential Diagnosis

11.3.8 Diagnosis

11.3.9 Management

11.4 Gigantism and Acromegaly. 11.4.1 Definition/Description

11.4.2 Frequency

11.4.3 Aetiology

11.4.4 Clinical Features

11.4.5 Radiographical Features

11.4.6 Diagnosis

11.4.7 Management

11.5 Brown Tumour of Hyperparathyroidism. 11.5.1 Definition/Description

11.5.2 Frequency

11.5.3 Aetiology

11.5.4 Clinical Features

11.5.5 Oral Manifestations

11.5.6 Radiographical Features

11.5.7 Microscopic Features

11.5.8 Differential Diagnosis

11.5.9 Diagnosis

11.5.10 Management

11.5.11 Prognosis

11.6 Paget's Disease of Bone (Osteitis Deformans) 11.6.1 Definition/Description

11.6.2 Frequency

11.6.3 Aetiology/Risk Factors

11.6.4 Clinical Features

11.6.5 Radiographical Features

11.6.6 Microscopic Features

11.6.7 Differential Diagnosis of Jaw Lesions

11.6.8 Diagnosis

11.6.9 Management

11.6.10 Prognosis

11.7 Fibrous Dysplasia and McCune–Albright Syndrome. 11.7.1 Definition/Description

11.7.2 Frequency

11.7.3 Aetiology

11.7.4 Clinical Features

11.7.5 Radiographical Features

11.7.6 Microscopic features

11.7.7 Differential Diagnosis

11.7.8 Diagnosis

11.7.9 Management

11.7.10 Prognosis

11.8 Mandibular and Palatine Tori: Key Features

11.9 Focal Osteoporotic Bone Marrow Defect: Key Features

Recommended Reading

12 Developmental Anomalies and Anatomical Variants of Oral Soft Tissues. CHAPTER MENU

12.1 Fordyce Granules: Key Features

12.2 Double Lip: Key Features

12.3 Leukoedema: Key Features

12.4 Ankyloglossia: Key Features

12.5 Geographic Tongue: Key Features

12.6 Hairy Tongue: Key Features

12.7 Fissured Tongue: Key Features

12.8 Lingual Thyroid: Key Features

12.9 Microglossia and Macroglossia: Key Features

12.10 Bifid Tongue: Key Features

12.11 Bifid Uvula: Key Features

12.12 Cleft Lip: Key Features

12.13 Calibre Persistent Labial Artery: Key Features

12.14 Epstein's Pearl and Bohn's Nodules: Key Features

12.15 Dermoid and Epidermoid Cysts: Key Features

12.16 Oral Varicosities: Key Features

12.17 Lymphoid Aggregates: Key Features

12.18 Parotid Papilla: Key Features

12.19 Circumvallate Papillae: Key Features

12.20 Physiological Pigmentation: Key Features

Recommended Reading

13 Bacterial Infections of the Oral Mucosa. CHAPTER MENU

13.1 Scarlet Fever: Key Features

13.2 Syphilis. 13.2.1 Definition/Description

13.2.2 Frequency

13.2.3 Aetiology/Risk Factors

13.2.4 Clinical Features

13.2.5 Microscopic Features

13.2.6 Differential Diagnosis

13.2.7 Diagnosis

13.2.8 Management

13.2.9 Prognosis

13.3 Gonorrhoea: Key Features

13.4 Tuberculosis. 13.4.1 Definition/Description

13.4.2 Frequency

13.4.3 Aetiology/Risk Factors

13.4.4 Clinical and Radiological Features

13.4.5 Microscopic Findings

13.4.6 Differential Diagnosis

13.4.7 Diagnosis

13.4.8 Management

13.4.9 Prognosis

Recommended Reading

14 Fungal Infections of the Oral Mucosa. CHAPTER MENU

14.1 Candidosis (Candidiasis) 14.1.1 Definition/Description

14.1.2 Frequency

14.1.3 Aetiology/Risk Factors

14.1.4 Clinical features

14.1.5 Microscopic features

14.1.6 Differential diagnosis

Diagnosis

14.1.7 Management

14.1.8 Prognosis

14.2 Histoplasmosis. 14.2.1 Definition/description

14.2.2 Frequency

14.2.3 Aetiology/risk factors

14.2.4 Clinical features

14.2.5 Microscopic features

14.2.6 Differential diagnosis

14.2.7 Diagnosis

14.2.8 Management

14.2.9 Prognosis

14.3 Blastomycosis: Key Features

Recommended Reading

15 Viral Infections of the Oral Mucosa. CHAPTER MENU

15.1 Primary Herpetic Gingivostomatitis (Primary Herpes) 15.1.1 Definition/Description

15.1.2 Frequency

15.1.3 Aetiology/Risk Factors

15.1.4 Clinical Features

15.1.5 Differential Diagnosis

15.1.6 Microscopic Features

15.1.7 Diagnosis

15.1.8 Management

15.1.9 Prognosis

15.2 Herpes Labialis. 15.2.1 Definition/Description

15.2.2 Frequency

15.2.3 Aetiology/Risk Factors

15.2.4 Clinical Features

15.2.5 Differential Diagnosis

15.2.6 Diagnosis

15.2.7 Management

15.2.8 Prognosis

15.3 Varicella (Chickenpox) 15.3.1 Definition/Description

15.3.2 Frequency

15.3.3 Aetiology/Risk Factors

15.3.4 Clinical Features

15.3.5 Differential Diagnosis

15.3.6 Diagnosis

15.3.7 Management

15.3.8 Prognosis

15.4 Herpes Zoster (Shingles) 15.4.1 Definition/Description

15.4.2 Frequency

15.4.3 Aetiology/Risk Factors

15.4.4 Clinical Features

15.4.5 Differential Diagnosis

15.4.6 Microscopic Features

15.4.7 Diagnosis

15.4.8 Management

15.4.9 Prognosis

15.5 Infectious Mononucleosis (Glandular Fever) 15.5.1 Definition/Description

15.5.2 Frequency

15.5.3 Aetiology/Risk Factors

15.5.4 Clinical Features

15.5.5 Differential Diagnosis

15.5.6 Laboratory Tests

15.5.7 Diagnosis

15.5.8 Management

15.6 Oral Hairy Leukoplakia: Key Features

15.7 Cytomegalovirus Infection: Key Features

15.8 Herpangina: Key Features

15.9 Hand, Foot, and Mouth Disease. 15.9.1 Definition/Description

15.9.2 Frequency

15.9.3 Aetiology

15.9.4 Clinical Features

15.9.5 Differential Diagnosis

15.9.6 Diagnosis

15.9.7 Management

15.9.8 Prognosis

15.10 Squamous Papilloma. 15.10.1 Definition/Description

15.10.2 Frequency

15.10.3 Aetiology/Risk Factors

15.10.4 Clinical Features

15.10.5 Microscopic Features

15.10.6 Differential Diagnosis

15.10.7 Diagnosis

15.10.8 Management

15.10.9 Prognosis

15.11 Condyloma Acuminatum: Key Features

15.12 Multifocal Epithelial Hyperplasia: Key Features

15.13 Verruca Vulgaris: Key Features

15.14 Measles: Key Features

Recommended Reading

16 Non‐infective Inflammatory Disorders of the Oral Mucosa. CHAPTER MENU

16.1 Recurrent Aphthous Stomatitis. 16.1.1 Definition/Description

16.1.2 Frequency

16.1.3 Aetiology/Risk Factors

16.1.4 Clinical Features

16.1.5 Differential Diagnosis

16.1.6 Microscopic Features

16.1.7 Diagnosis

16.1.8 Management

16.1.9 Prognosis

16.2 Oral Lichen Planus. 16.2.1 Definition/Description

16.2.2 Frequency

16.2.3 Aetiology

16.2.4 Clinical Features

16.2.5 Microscopic Features

16.2.6 Differential Diagnosis

16.2.7 Diagnosis

16.2.8 Management

16.2.9 Prognosis

16.3 Oral Lichenoid Lesions. 16.3.1 Definition/Description

16.3.2 Frequency

16.3.3 Aetiology/Risk Factors

16.3.4 Clinical Features

16.3.5 Microscopic Features

16.3.6 Differential Diagnosis

16.3.7 Diagnosis

16.3.8 Management

16.3.9 Prognosis

16.4 Pemphigus Vulgaris. 16.4.1 Definition/Description

16.4.2 Pemphigus Vulgaris

16.4.3 Frequency

16.4.4 Aetiology/Risk Factors

16.4.5 Clinical Features

16.4.6 Microscopic Features

16.4.7 Differential Diagnosis

16.4.8 Diagnosis

16.4.9 Management

16.4.10 Prognosis

16.5 Mucous Membrane Pemphigoid. 16.5.1 Definition/Description

16.5.2 Frequency

16.5.3 Aetiology

16.5.4 Clinical Features

16.5.5 Microscopic Features

16.5.5.1 Immunofluorescence Findings

16.5.6 Differential Diagnosis

16.5.7 Diagnosis

16.5.8 Management

16.5.9 Prognosis

16.6 Erythema Multiforme. 16.6.1 Definition/Description

16.6.2 Frequency

16.6.3 Aetiology

16.6.4 Clinical Features

16.6.5 Microscopic Features

16.6.6 Differential Diagnosis

16.6.7 Diagnosis

16.6.8 Management

16.6.9 Prognosis

16.7 Lupus Erythematosus: Key Features

16.8 Traumatic Ulcer: Key Features

16.9 Oral Lesions in Behcet's Disease/Syndrome. 16.9.1 Definition/Description

16.9.2 Frequency

16.9.3 Aetiology

16.9.4 Clinical Features

16.9.5 Differential Diagnosis

16.9.6 Diagnosis

16.9.7 Management

16.9.8 Prognosis

16.10 Oral Lesions in Crohn's Disease. 16.10.1 Definition/Description

16.10.2 Frequency

16.10.3 Aetiology/Risk factors

16.10.4 Clinical Features

16.10.5 Differential Diagnosis

16.10.6 Diagnosis

16.10.7 Management

16.10.8 Prognosis

16.11 Oral Lesions in Reactive Arthritis: Key Features

16.12 Uremic Stomatitis: Key Features

16.13 Chronic Ulcerative Stomatitis: Key Features

16.14 Radiation‐Induced Mucositis: Key Features

16.15 Medication‐Induced Oral Ulceration: Key Features

16.16 Stevens–Johnson Syndrome and Toxic Epidermal Necrolysis. 16.16.1 Definition/Description

16.16.2 Frequency

16.16.3 Aetiology/Risk Factors

16.16.4 Clinical Features

16.16.5 Differential Diagnosis

16.16.6 Diagnosis

16.16.7 Management

16.16.8 Prognosis

Recommended Reading

17 Non‐neoplastic Mucosal Swellings. CHAPTER MENU

17.1 Irritation Fibroma (Traumatic Fibroma) 17.1.1 Definition/Description

17.1.2 Frequency

17.1.3 Aetiology

17.1.4 Clinical Features

17.1.5 Microscopic Features

17.1.6 Differential Diagnosis

17.1.7 Diagnosis

17.1.8 Management

17.1.9 Prognosis

17.2 Denture‐Induced Granuloma (Epulis Fissuratum) 17.2.1 Definition/Description

17.2.2 Frequency

17.2.3 Aetiology/Risk Factors

17.2.4 Clinical Features

17.2.5 Microscopic Features

17.2.6 Differential Diagnosis

17.2.7 Diagnosis

17.2.8 Management

17.3 Fibrous Epulis (Peripheral Fibroma): Key Features

17.4 Pyogenic Granuloma: Key Features

17.5 Peripheral Giant Cell Granuloma: Key Features

17.6 Peripheral Ossifying Fibroma: Key Features

17.7 Traumatic Neuroma. 17.7.1 Definition/Description

17.7.2 Frequency

17.7.3 Aetiology/Risk Factors

17.7.4 Clinical Features

17.7.5 Microscopic Features

17.7.6 Differential Diagnosis

17.7.7 Diagnosis

17.7.8 Management

17.7.9 Prognosis

17.8 Squamous Papilloma: Key Features

17.9 Congenital Epulis: Key Features

Recommended Reading

18 Benign Neoplasms of the Oral Mucosa. CHAPTER MENU

18.1 Lipoma. 18.1.1 Definition/Description

18.1.2 Frequency

18.1.3 Aetiology

18.1.4 Clinical Features

18.1.5 Microscopic Features

18.1.6 Differential Diagnosis

18.1.7 Diagnosis

18.1.8 Management

18.1.9 Prognosis

18.2 Schwannoma (Neurilemmoma) 18.2.1 Definition/Description

18.2.2 Frequency

18.2.3 Aetiology/Origin

18.2.4 Clinical Features

18.2.5 Microscopic Features

18.2.6 Differential Diagnosis

18.2.7 Diagnosis

18.2.8 Management

18.2.9 Prognosis

18.3 Granular Cell Tumour. 18.3.1 Definition/Description

18.3.2 Frequency

18.3.3 Aetiology/Origin

18.3.4 Clinical Features

18.3.5 Microscopic Features

18.3.6 Differential Diagnosis

18.3.7 Diagnosis

18.3.8 Management

18.3.9 Prognosis

18.4 Haemangioma. 18.4.1 Definition/Description

18.4.2 Frequency

18.4.3 Aetiology/Origin

18.4.4 Clinical Features

18.4.5 Microscopic Features

18.4.6 Differential Diagnosis

18.4.7 Diagnosis

18.4.8 Management

18.4.9 Prognosis

18.5 Lymphangioma. 18.5.1 Definition/Description

18.5.2 Frequency

18.5.3 Aetiology/Origin

18.5.4 Clinical Features

18.5.5 Microscopic Features

18.5.6 Differential Diagnosis

18.5.7 Diagnosis

18.5.8 Management

18.5.9 Prognosis

18.6 Leiomyoma (Vascular Leiomyomas): Key Features

18.7 Rhabdomyoma: Key Features

Recommended Reading

19 Oral Potentially Malignant Disorders. CHAPTER MENU

19.1 Erythroplakia. 19.1.1 Definition/Description

19.1.2 Frequency

19.1.3 Aetiology/Risk Factors

19.1.4 Clinical Signs and Symptoms

19.1.5 Microscopic Features

19.1.6 Differential Diagnosis

19.1.7 Diagnosis

19.1.8 Management

19.1.9 Prognosis

19.1.10 Special Considerations

19.2 Leukoplakia. 19.2.1 Definition/Description

19.2.2 Frequency

19.2.3 Aetiology/Risk Factors

19.2.4 Clinical Features

19.2.5 Microscopic Features

19.2.6 Differential Diagnosis

19.2.7 Diagnosis

19.2.8 Management/Prevention

19.2.9 Prognosis

19.2.10 Special Considerations

19.3 Chronic Hyperplastic Candidosis (Candidal Leukoplakia) 19.3.1 Definition/Description

19.3.2 Frequency

19.3.3 Aetiology/Risk Factors

19.3.4 Clinical Features

19.3.5 Microscopic Features

19.3.6 Differential Diagnosis

19.3.7 Diagnosis

19.3.8 Management/Prevention

19.3.9 Prognosis

19.3.10 Special Considerations

19.4 Palatal Lesions in Reverse Smokers. 19.4.1 Definition/Description

19.4.2 Frequency

19.4.3 Aetiology/Risk Factors

19.4.4 Clinical Features

19.4.5 Microscopic Features

19.4.6 Differential Diagnosis

19.4.7 Diagnosis

19.4.8 Management

19.4.9 Prognosis

19.5 Oral Lichen Planus: Key Features

19.6 Oral Submucous Fibrosis. 19.6.1 Definition/Description

19.6.2 Frequency

19.6.3 Aetiology/Risk Factors

19.6.4 Clinical Features

19.6.5 Microscopic Features

19.6.6 Differential Diagnosis

19.6.7 Diagnosis

19.6.8 Management

19.6.9 Prognosis

19.7 Oral Lichenoid Lesion. 19.7.1 Definition/Description

19.7.2 Frequency

19.7.3 Aetiology/Risk Factors

19.7.4 Clinical Features

19.7.5 Microscopic Features

19.7.6 Differential Diagnosis

19.7.7 Diagnosis

19.7.8 Management

19.7.9 Prognosis

19.8 Lupus Erythematosus. 19.8.1 Definition/Description

19.8.2 Frequency

19.8.3 Aetiology/Risk Factors

19.8.4 Clinical Signs and Symptoms

19.8.5 Microscopic Features

19.8.6 Differential Diagnosis

19.8.7 Diagnosis

19.8.8 Management

19.8.9 Prognosis

19.9 Actinic Keratosis of the Lip (Actinic Cheilitis) 19.9.1 Definition/Description

19.9.2 Frequency

19.9.3 Aetiology/Risk Factors

19.9.4 Clinical Signs and Symptoms

19.9.5 Microscopic Features

19.9.6 Differential Diagnosis

19.9.7 Diagnosis

19.9.8 Management

19.9.9 Prognosis

19.10 Graft‐Versus‐Host Disease. 19.10.1 Definition/Description

19.10.2 Frequency

19.10.3 Aetiology/Risk Factors. 19.10.3.1 Risk Factors

19.10.4 Clinical Features

19.10.5 Microscopic Features

19.10.6 Differential Diagnosis

19.10.7 Diagnosis

19.10.8 Management

19.10.9 Prognosis

19.11 Dyskeratosis Congenita. 19.11.1 Definition/Description

19.11.2 Frequency

19.11.3 Risk Factors/Aetiology

19.11.4 Clinical Features

19.11.5 Microscopic Features

19.11.6 Differential Diagnosis

19.11.7 Diagnosis

19.11.8 Management

19.11.9 Prognosis

19.12 Sublingual Keratosis: Key Features

19.13 Syphilitic Leukoplakia: Key Features

19.14 Darier's Disease: Key Features

Recommended Reading

20 Malignant Neoplasms of the Oral Mucosa. CHAPTER MENU

20.1 Squamous Cell Carcinoma and Verrucous Carcinoma. 20.1.1 Definition/Description

20.1.2 Frequency

20.1.3 Aetiology/Risk Factors

20.1.4 Clinical Features

20.1.5 Microscopic Features

20.1.6 Differential Diagnosis

20.1.7 Diagnosis

20.1.8 Management

20.1.9 Prognosis

20.2 Melanoma (Malignant Melanoma) 20.2.1 Definition/Description

20.2.2 Frequency

20.2.3 Aetiology/Risk Factors

20.2.4 Clinical Features

20.2.5 Microscopic Feature

20.2.6 Differential Diagnosis

20.2.7 Diagnosis

20.2.8 Management

20.2.9 Prognosis

20.3 Kaposi's Sarcoma. 20.3.1 Definition/Description

20.3.2 Frequency

20.3.3 Aetiology

20.3.4 Clinical Features

20.3.5 Microscopic Features

20.3.6 Differential Diagnosis

20.3.7 Diagnosis

20.3.8 Management

20.3.9 Prognosis

20.4 Fibrosarcoma: Key Features

20.5 Rhabdomyosarcoma: Key Features

20.6 Leiomyosarcoma: Key Features

Recommended Readings

21 Non‐neoplastic Salivary Gland Diseases. CHAPTER MENU

21.1 Salivary Calculi: Key Features

21.2 Mucoceles (Mucous Extravasation Cysts, Mucous Retention Cysts and Ranula) 21.2.1 Definition/Description

21.2.2 Frequency

21.2.3 Aetiology

21.2.4 Clinical Features

21.2.5 Microscopic Features

21.2.6 Differential Diagnosis

21.2.7 Diagnosis

21.2.8 Management

21.2.9 Prognosis

21.3 Sjögren's Syndrome. 21.3.1 Definition/Description

21.3.2 Frequency

21.3.3 Aetiology/Risk Factors

21.3.4 Clinical Features

21.3.5 Microscopic Features

21.3.6 Differential Diagnosis

21.3.7 Diagnosis

21.3.8 Management

21.3.9 Prognosis

21.4 Sialadenitis: Key Features

21.5 Necrotizing Sialometaplasia: Key Features

Recommended Reading

22 Salivary Gland Neoplasms. CHAPTER MENU

22.1 World Health Organization Histological Classification of Salivary Gland Tumours (2017)

22.2 Pleomorphic Adenoma. 22.2.1 Definition/Description

22.2.2 Frequency

22.2.3 Aetiology/Risk Factors

22.2.4 Clinical Features

22.2.5 Microscopic Features

22.2.6 Differential Diagnosis

22.2.7 Diagnosis

22.2.8 Management

22.2.9 Prognosis

22.3 Warthin's Tumour (Papillary Cystadenoma Lymphomatosum) 22.3.1 Definition/Description

22.3.2 Frequency

22.3.3 Aetiology

22.3.4 Clinical Features

22.3.5 Microscopic Features

22.3.6 Differential Diagnosis

22.3.7 Diagnosis

22.3.8 Management

22.3.9 Prognosis

22.4 Mucoepidermoid Carcinoma. 22.4.1 Definition/Description

22.4.2 Frequency

22.4.3 Aetiology

22.4.4 Clinical Features

22.4.5 Microscopic Features

22.4.6 Differential Diagnosis

22.4.7 Diagnosis

22.4.8 Management/Prognosis

22.5 Adenoid Cystic Carcinoma. 22.5.1 Definition/Description

22.5.2 Frequency

22.5.3 Aetiology

22.5.4 Clinical Features

22.5.5 Microscopic Features

22.5.6 Differential Diagnosis

22.5.7 Diagnosis

22.5.8 Management

22.5.9 Prognosis

Recommended Reading

23 White Lesions of the Oral Mucosa

23.1 Actinic Cheilitis: Key Features

23.2 Chemical Burn: Key Features

23.3 Chronic Hyperplastic Candidosis: Key Features

23.4 Darier's Disease: Key Features

23.5 Dyskeratosis Congenita: Key Features

23.6 Fordyce Granules: Key Features

23.7 Frictional Keratosis: Key Features

23.8 Hereditary Benign Intraepithelial Dyskeratosis: Key Features

23.9 Leukoedema: Key Features

23.10 Leukoplakia: Key Features

23.11 Oral Hairy Leukoplakia: Key Features

23.12 Oral Lichen Planus: Key Features

23.13 Oral Squamous Cell Carcinoma: Key Features

23.14 Pseudomembranous Candidosis: Key Features

23.15 Smokeless Tobacco‐Induced Keratosis: Key Features

23.16 Smoker's Keratosis: Key Features

23.17 Sublingual Keratosis: Key Features

23.18 Syphilitic Leukoplakia: Key Features

23.19 Verrucous Carcinoma: Key Features

23.20 White Hairy Tongue: Key Features

23.21 White Sponge Nevus: Key Features

Recommended Reading

24 Red and Purple Lesions of the Oral Mucosa

24.1 Contact Stomatitis: Key Features

24.2 Desquamative Gingivitis: Key Features

24.3 Erythema Migrans: Key Features

24.4 Erythema Multiforme: Key Features

24.5 Erythematous Candidosis: Key Features

24.6 Erythroplakia: Key Features

24.7 Haemangioma: Key Features

24.8 Hereditary Haemorrhagic Telangiectasia: Key Features

24.9 Infectious Mononucleosis: Key Features

24.10 Kaposi's Sarcoma: Key Features

24.11 Linear Gingival Erythema: Key Features

24.12 Lupus Erythematosus: Key Features

24.13 Median Rhomboid Glossitis: Key Features

24.14 Mucosal Ecchymosis, Haematoma, and Petechiae: Key Features

24.15 Plasma Cell Gingivitis: Key Features

24.16 Port‐Wine Nevus: Key Features

24.17 Radiation Mucositis: Key Features

24.18 Thermal Burn: Key Features

Recommended Reading

25 Blue, Black, and Brown Lesions of the Oral Mucosa

25.1 Addison's Disease: Key Features

25.2 Amalgam Tattoo: Key Features

25.3 Black/Brown Hairy Tongue: Key Features

25.4 Drug‐Induced Pigmentation: Key Features

25.5 Heavy Metal Pigmentation: Key Features

25.6 Laugier–Hunziker Syndrome: Key Features

25.7 Melanoma: Key Features

25.8 Melanotic Macule: Key Features

25.9 Peutz–Jeghers Syndrome: Key Features

25.10 Physiological Pigmentation: Key Features

25.11 Mucosal Nevi: Key Features

25.12 Smoker's Melanosis: Key Features

Recommended Reading

26 Vesiculobullous Lesions of the Oral Mucosa

26.1 Angina Bullosa Haemorrhagica: Key Features

26.2 Bullous Lichen Planus: Key Features

26.3 Dermatitis Herpetiformis: Key Features

26.4 Erythema Multiforme: Key Features

26.5 Hand, Foot and Mouth Disease: Key Features

26.6 Herpes Zoster (Shingles): Key Features

26.7 Mucous Membrane Pemphigoid: Key Features

26.8 Pemphigus Vulgaris: Key Features

26.9 Primary Herpetic Gingivostomatitis: Key Features

26.10 Herpes Labialis: Key Features

Recommended Reading

27 Ulcerative Lesions of the Oral Mucosa

27.1 Oral Ulcers in Agranulocytosis: Key Features

27.2 Oral Ulcers in Behçet’s Disease: Key Features

27.3 Oral Ulcers in Coeliac Disease: Key Features

27.4 Chronic Ulcerative Stomatitis: Key Features

27.5 Oral Ulcers in Crohn's Disease: Key Features

27.6 Oral Ulcers in Cyclic Neutropenia: Key Features

27.7 Cytomegalovirus Ulcers: Key Features

27.8 Eosinophilic Ulcer: Key Features

27.9 Gangrenous Stomatitis: Key Features

27.10 Necrotizing Sialometaplasia: Key Features

27.11 Necrotizing Ulcerative Gingivitis: Key Features

27.12 Oral Ulcers in Reactive Arthritis: Key Features

27.13 Recurrent Aphthous Ulcers: Key Features

27.14 Squamous Cell Carcinoma Presenting as an Ulcer: Key Features

27.15 Syphilitic Ulcers: Key Features

27.16 Traumatic Ulcer: Key Features

27.17 Tuberculous Ulcer: Key Features

27.18 Oral Ulcer in Ulcerative Colitis: Key Features

Recommended Reading

28 Papillary Lesions of the Oral Mucosa

28.1 Condyloma Acuminatum: Key Features

28.2 Multifocal Epithelial Hyperplasia (Heck's Disease): Key Features

28.3 Oral Proliferative Verrucous Leukoplakia: Key Features

28.4 Squamous Papilloma: Key Features

28.5 Squamous Cell Carcinoma: Key Features

28.6 Verruca Vulgaris (Oral Warts): Key Features

28.7 Verrucous Carcinoma: Key Features

Recommended Reading

29 Orofacial Pain

29.1 Odontogenic Orofacial Pain. 29.1.1 Pulpitis/Dentine Hypersensitivity

29.1.2 Apical Periodontitis or Infected Root Canal

29.1.3 Fractured or Cracked Tooth

29.1.4 Spreading Odontogenic Infection Without Severe or Systemic Features

29.1.5 Cellulitis/Ludwig Angina with Systemic Features

29.1.6 Dry Socket

29.2 Neuropathic Orofacial Pain. 29.2.1 Trigeminal Neuralgia

29.2.2 Glossopharyngeal Neuralgia

29.2.3 Post‐herpetic Neuralgia

29.2.4 Burning Mouth Syndrome

29.3 Other Conditions with Orofacial Pain. 29.3.1 Acute Necrotizing Ulcerative Gingivitis

29.3.2 Temporomandibular Joint Disorders

29.3.3 Atypical Facial Pain (Persistent Idiopathic Facial Pain)

29.3.4 Migraine

29.3.5 Sinusitis

29.3.6 Temporal Arteritis (Giant Cell Arteritis)

29.3.7 Cardiogenic Jaw Pain

29.3.8 Sialolithiasis (Salivary Calculus)

Recommended Reading

30 Oral Manifestations of Systemic Disorders

30.1 Gastrointestinal and Liver Disorders. 30.1.1 Gastroesophageal Reflux Disease

30.1.2 Bulimia and Anorexia

30.1.3 Crohn's Disease

30.1.4 Ulcerative Colitis

30.1.5 Coeliac Disease

30.1.6 Irritable Bowel Syndrome

30.1.7 Alcoholic Liver Disease

30.1.8 Liver Cirrhosis

30.2 Cardiovascular Disease. 30.2.1 Angina Pectoris and Myocardial Infarction

30.2.2 Congenital Heart Disease

30.2.3 Rheumatic Fever/Infective Endocarditis

30.2.4 Hypertension

30.3 Respiratory Disease. 30.3.1 Chronic Obstructive Pulmonary Disease

30.3.2 Lung Abscess and Bronchiectasis

30.3.3 Pulmonary Tuberculosis

30.3.4 Cystic Fibrosis

30.4 Kidney Diseases. 30.4.1 Chronic Kidney Failure

30.4.2 Nephrotic Syndrome

30.4.3 Patients on Kidney Dialysis

30.5 Endocrine and Metabolic Disorders. 30.5.1 Hyperthyroidism

30.5.2 Hypothyroidism

30.5.3 Hypopituitarism

30.5.4 Hyperpituitarism (Acromegaly)

30.5.5 Diabetes Insipidus

30.5.6 Addison's Disease (Adrenal Insufficiency)

30.5.7 Cushing's Disease (Adrenocortical Excess)

30.5.8 Diabetes Mellitus

30.5.9 Hypocalcaemia

30.5.10 Hypercalcaemia

30.6 Nervous System Disorders. 30.6.1 Stroke

30.6.2 Epilepsy

30.6.3 Parkinson's Disease

30.6.4 Multiple Sclerosis

30.6.5 Myasthenia Gravis

30.6.6 Bell's Palsy

30.7 Haematological Disorders. 30.7.1 Anaemia

30.7.2 Thrombocytopenia

30.7.3 Haemophilia

30.7.4 Leukaemia

30.7.5 Multiple Myeloma

30.7.6 Non‐Hodgkin Lymphoma

30.7.7 Burkitt's Lymphoma

30.8 Immune System Disorders. 30.8.1 Allergic Contact Stomatitis

30.8.2 Angioedema

30.8.3 Sjögren's Syndrome

30.8.4 Temporal Arteritis

30.8.5 Granulomatosis with Polyangiitis (Wegener's Granulomatosis)

30.8.6 Behçet’s Disease

30.8.7 HIV/AIDS

Reference

Recommended Reading

31 Systemic Diseases Associated with Periodontal Infections

31.1 Cardiovascular Disease

31.2 Coronary Heart Disease (Atherosclerosis and Myocardial Infarction)

31.3 Stroke

31.4 Infective Endocarditis

31.5 Bacterial Pneumonia

31.6 Low Birth Weight

31.7 Diabetes Mellitus

Recommended Reading

32 Other Signs and Symptoms Related to the Oral Environment

32.1 Halitosis

32.2 Taste Disorders

32.3 Dry Mouth (Xerostomia)

32.4 Sialorrhea

32.5 Trismus

32.6 COVID‐19 Infection

Recommended Reading

33 Outline of Diagnostic Steps and Procedures Employed in Oral Pathology and Oral Medicine

33.1 History. 33.1.1 General Framework of History Taking

33.2 Clinical Examination. 33.2.1 Extraoral Examination

33.2.2 Intraoral Examination

33.2.3 Palpation

33.2.4 Assessment of Oral Problem

33.3 Clinical Differential Diagnosis. 33.3.1 Definition/Description

33.4 Diagnosis. 33.4.1 Biopsy

33.4.2 Histopathology

33.4.3 Microbiology

33.4.4 Blood Tests

33.4.5 Imaging

33.4.6 Other Tests

33.4.7 Referral Letter

Recommended Reading

Index

a

b

c

d

e

f

g

h

i

j

k

l

m

n

o

p

r

s

t

u

v

w

x

WILEY END USER LICENSE AGREEMENT

Отрывок из книги

S. R. Prabhu BDS; MDS (Oral Path); FFDRCS (Oral Med); FDSRCS (Edin); FDSRCPS (Glas); FDSRCS (Eng), FFGDPRCS (UK); MOMed RCS (Edin); FICD.

Honorary Associate ProfessorSchool of DentistryUniversity of QueenslandBrisbane, Australia

.....

.....

Добавление нового отзыва

Комментарий Поле, отмеченное звёздочкой  — обязательно к заполнению

Отзывы и комментарии читателей

Нет рецензий. Будьте первым, кто напишет рецензию на книгу Handbook of Oral Pathology and Oral Medicine
Подняться наверх