Thanks to its innovative contents and the internship it offers, this program is perfect for dentists who want to update their knowledge in both a quick and easy way”

This Hybrid Master's Degree in Oral Medicine is aimed at providing the dentist with an in-depth knowledge of the diagnosis and differentiation of the different benign and malignant lesions of the oral cavity and its adjoining tissues, including diagnostic and surgical techniques. It is also intended for the professional to master the different types of treatment, professional application and preventive utility.

It is, therefore, a branch that complements the rest of specialties, which is a fundamental pillar prior to carrying out any treatment. Moreover, thanks to this program, dentists will be able to avoid negligence due to lack of knowledge and, at the same time, will be equipped to detect and rehabilitate pathologies with the latest tools on the market.

This degree is characterized by its dynamic methodology, which intersperses clinical cases for dentists to identify and associate the topics covered with real images. At the same time, students will have access to questionnaires where they can evaluate and test their knowledge. The objective is to bring students as close as possible to the situations they will encounter on in its practice daily basis so as to be able to approach and manage them in a coordinated, efficient and planned manner, using the best and most modern methods.

This program is carried out in a 100% online format that will adapt to professional circumstances, since they will be able to study whenever and wherever they wish. For this purpose, the best multimedia resources will be available to make the process of deepening student knowledge as effective and simple as possible. Thus, students will be able to access all the program materials 24 hours a day.

After completing that stage of the program, professionals will have the opportunity to undergo an internship in a high prestigious clinical center. This internship will take place over 3 weeks, during which time you will not only be supervised by specialists from the clinical center itself, but you will also have access to its equipment and handle patients. It is therefore a unique opportunity to be updated in a completely real environment.

The theoretical-practical and 100% online itinerary is combined with an intensive 3-week internship in a leading dental clinic, which will prepare specialists to face all the present and future challenges in this area”

This Hybrid Master's Degree in Oral Medicine contains the most complete and up-to-date scientific program on the market. The most important features include:

• More than 100 clinical cases presented by professional Dentistry experts in Oral Medicine
• The graphic, schematic and practical contents of which they are composed provide scientific and practical information on the odontology disciplines that are essential for professional practice
• The eminently practical approach
• Updated content, which compile the latest trends in Oral Medicine
• The multimedia resources, put together to facilitate learning
• All of this will be complemented by theoretical lessons, questions to the expert, debate forums on controversial topics, and individual reflection assignments
• Content that is accessible from any fixed or portable device with an Internet connection
• Furthermore, you will be able to carry out a clinical internship in one of the best hospitals in the world

This Hybrid Master's Degree is a unique opportunity to get up to date in Oral Medicine, as it offers direct contact with prestigious specialists and real patients”

This Hybrid Master's Degree is aimed at updating dentistry professionals who wish to deepen their knowledge on new techniques in the field of Oral Medicine. The content is based on the latest scientific evidence and organized in a didactic way to integrate theoretical knowledge into nursing practice.

Thanks to the multimedia content, developed with the latest educational technology, dental professionals will benefit from situated and contextual learning, i.e., a simulated environment that will provide immersive learning programmed to train in real situations. This program is designed around Problem-Based Learning, whereby the professional must try to solve the different professional practice situations that arise throughout the program. For this purpose, the student will be assisted by an innovative interactive video system created by renowned experts.

This program will allow you to delve into the most advanced techniques for the therapeutic management of disorders that may affect the buccal mucosa, salivary glands, bone tissue or soft tissue of the buccomaxillofacial area"

Update yourself in a comfortable way, deciding the pace of study and when to pass the theoretical-practical part of this degree, and then enjoy participating in the day-to-day work of a dental clinic with the most advanced technology and procedures"

The syllabus of this degree has been designed taking into account the latest procedures existing in this sector, by the highly prestigious teaching team that makes up this Master's Degree. Thus, a curriculum with a broad vision and perspective on Oral Medicine has been established, which allows to approach the different oral and maxillofacial pathologies from the interface of Medicine and Odontology. Therefore, the student will deepen in aspects such as applied anatomopathology, elementary lesions, inflammatory and infectious oral pathology or the pathology of the salivary glands, among others.

This program will allow you to integrate the latest advances in Oral Medicine into your daily practice, giving you the opportunity to offer new services to your patients and users"

Module 1. Oral Medicine and Diagnostic Methods

1.1. Pathology and Oral Medicine

1.1.1. In-Depth Oral Medicine
1.1.2. Relevant Figures
1.1.3. Oral Medicine applied to health branches
1.1.4. Current Uses of Oral Medicine in Odontology
1.1.5. Advances and Technology

1.2. Medical History

1.2.1. Medical History
1.2.2. Personal and Family History
1.2.3. Exploration
1.2.4. Diagnosis
1.2.5. Treatment Plan

1.3. Informed Consent

1.3.1. Origins and Fundamentals
1.3.2. Features
1.3.3. Applicable Exceptions
1.3.4. The Right to Information
1.3.5. The Right to Confidentiality

1.4. Legal Implications in Health Care

1.4.1. Origin and Fundamentals
1.4.2. Legal Principles Applied to Health Care
1.4.3. Obligations and Rights of the Professional
1.4.4. Legal Relevance of Medical Records
1.4.5. Relation between Health Care and Administrative Management

1.5. Complementary Tests

1.5.1. Radiography
1.5.2. Nuclear Magnetic Resonance (NMR)
1.5.3. CT or CBCT
1.5.4. Electromyography
1.5.5. Sialometry
1.5.6. Ultrasound
1.5.7. Analytics
1.5.8. Urinalysis
1.5.9. Capillary Glycemia
1.5.10. INR
1.5.11. Exudates
1.5.12. FNA, Biopsy and Cytology
1.5.13. Mantoux Test
1.5.14. Breath Test
1.5.15. Endocrine Tests
1.5.16. Pulse Oximetry and Densimetry
1.5.17. Photography

1.6. Radiography

1.6.1. Intraoral X-Rays Types
1.6.2. Extraoral X-Rays Projections

1.7. Diagnostic Tests in Oral Medicine

1.7.1. Clinical Tests
1.7.2. Patch Test
1.7.3. Diagnostic Imaging
1.7.4. Contrast Diagnostics
1.7.5. Nuclear medicine
1.7.6. Culture Techniques
1.7.7. Immunological and Immunohistochemical Techniques

1.8. Biopsy

1.8.1. Fundamentals
1.8.2. Indications and applications
1.8.3. Types and procedures
1.8.4. Most Frequent Errors
1.8.5. Contraindications for biopsy techniques

1.8.5.1. Materials
1.8.5.2. Incisional
1.8.5.3. Excisional
1.8.5.4. FNA
1.8.5.5. Cytology

1.9. Validity of Diagnostic Tests

1.9.1. Sensitivity
1.9.2. Specificity
1.9.3. Security/Safety
1.9.4. Predictive Values
1.9.5. Accuracy
1.9.6. Precision

1.10. Research

1.10.1. Observation or Research?
1.10.2. Types of Studies
1.10.3. Systematic Reviews
1.10.4. Meta-analytical study
1.10.5. Clinical Trials
1.10.6. Publication and Scientific Articles: Criteria

Module 2. Applied Anatomopathology and Elementary Lesions

2.1. Pathology Branches

2.1.1. General Pathology
2.1.2. Systemic Pathology
2.1.3. Molecular Pathology
2.1.4. Molecular Biology
2.1.5. Dental and Health Care Applications

2.2. Oral Mucosal Histopathology

2.2.1. Anatomy Recap
2.2.2. Histological Structure
2.2.3. Microscopic Elementary Lesions of the Oral Mucosa
2.2.4. Epithelial Tissue

2.2.4.1. Keratinized
2.2.4.2. Non-Keratinized

2.2.5. Epithelial Cell Junctions

2.2.5.1. Desmosomics
2.2.5.2. Hemidesmosomics
2.2.5.3. Others

2.3. Pathological Anatomy Fundamentals

2.3.1. Applications
2.3.2. Techniques
2.3.3. Study Method

2.3.3.1. Autopsy
2.3.3.2. Experimental Method

2.4. Functional Classification of Oral Mucosa

2.4.1. External Labial Mucosa
2.4.2. Lining Mucosa
2.4.3. Specialized Mucosa

2.5. Elemental Lesions

2.5.1. Features
2.5.2. Classification
2.5.3. Etiology
2.5.4. Chemical Agents

2.5.4.1. Chemical Burns: Substances and Drugs
2.5.4.2. Necrosis Post Anestesia
2.5.4.3. Secondary Drug Lesions

2.5.5. Physical Agents

2.5.5.1. Burns

2.5.5.1.1. Thermal
2.5.5.1.2. Electrical

2.5.6. Mechanical Agents

2.5.6.1. Alba Line
2.5.6.2. Frictional Hyperkeratosis
2.5.6.3. Leukoedema
2.5.6.4. Nibbling
2.5.6.5. Trauma
2.5.6.6. Ulcers

2.5.6.6.1. Decubitus
2.5.6.6.2. Traumatic

2.5.7. Allergic Oral Pathology

2.5.7.1. Angioedema
2.5.7.2. Allergic Contact Stomatitis
2.5.7.3. Anaphylactic Shock

2.5.8. Yatrogenia

2.6. Solid Content Primary Lesions

2.6.1. Macula
2.6.2. Papule
2.6.3. Nodes
2.6.4. Habon
2.6.5. Tuber
2.6.6. Rubber
2.6.7. Keratosis
2.6.8. Tumours

2.7. Liquid Content Primary Lesions

2.7.1. Flictena
2.7.2. Gall Bladder
2.7.3. Blister
2.7.4. Pustules
2.7.5. Cyst

2.8. Secondary Lesions

2.8.1. Continuity Solution
2.8.2. Disposible Residue
2.8.3. Restorative Processes

2.9. Staining

2.9.1. Oral Mucosa Dyschromia
2.9.2. Exogenous
2.9.3. Endogenous

2.10. Other Lesions

2.10.1. Sclerosis
2.10.2. Ulcera and Erosion
2.10.3. Lichenification
2.10.4. Intertrigo
2.10.5. Infiltration
2.10.6. Ocular Involvement

Module 3. Inflammatory and Infectious Oral Pathology

3.1. Bacterial Infections

3.1.1. Features
3.1.2. Scarlet Fever
3.1.3. Impetigo
3.1.4. Angular Cheilitis
3.1.5. Telangiectatic Granuloma
3.1.6. Cellulite

3.1.6.1. Acute
3.1.6.2. Chronic

3.1.7. Necrotizing Gingivitis
3.1.8. Gonococcal Pharyngitis
3.1.9. Syphilis

3.1.9.1. Primary
3.1.9.2. Secondary
3.1.9.3. Tertiary

3.1.10. Tuberculosis
3.1.11. Leprosy
3.1.12. Actinomycosis
3.1.13. Gonorrhoea
3.1.14. Adenitis
3.1.15. Fistulas

3.2. Fungal Infections

3.2.1. Etiology
3.2.2. Classification

3.2.2.1. Thrush or Acute Pseudomembranous Candidiasis
3.2.2.2. Candidiasis Erythematosis
3.2.2.3. Leukoplasiform Candidiasis
3.2.2.4. Erythematous Candidiasis: Erosive Atrophic
3.2.2.5. Angular Cheilitis
3.2.2.6. Rhomboid Glossitis
3.2.2.7. Prosthetic Stomatitis
3.2.2.8. Deep Mucositis
3.2.2.9. Blastomycosis

3.3. Viral Infections

3.3.1. Characteristics and Treatment
3.3.2. Papillomas
3.3.3. Warts
3.3.4. Focal Epithelial Hyperplasia
3.3.5. Condyloma Acuminatum
3.3.6. Florida Oral Condylomatosis
3.3.7. HSV Recurrent Herpes Labialis
3.3.8. Herpetic Primoinfection, Varicella Zoster and Herpes Zoster
3.3.9. Molluscum Contagiosum
3.3.10. Coxsackie
3.3.11. Herpangina
3.3.12. Hand-Foot-Mouth Disease
3.3.13. Paramyxovirus
3.3.14. Measles
3.3.15. CMV Mononucleosis
3.3.16. Epstein-Barr
3.3.17. Kawasaki Syndrome

3.4. Benign Exophytic Lesions

3.4.1. Etiology
3.4.2. Reactive Hyperplasia

3.4.2.1. Fibroepithelial Hyperplasia
3.4.2.2. Diapneusia
3.4.2.3. Papillary Palatine Hyperplasia
3.4.2.4. Fissured Granuloma
3.4.2.5. Fibrous Nodule
3.4.2.6. Reactive Granulomas
3.4.2.7. Giant Cell Peripheral

3.4.3. Salivary Cysts

3.4.3.1. Caused by Retention
3.4.3.2. Caused by Extravasation

3.4.4. Benign Tumors

3.4.4.1. Epithelial
3.4.4.2. Connective

3.5. Connective Tissue Alterations

3.5.1. Sjögren’s Syndrome
3.5.2. Lupus Erythematosus
3.5.3. Systemic Sclerosis
3.5.4. Rheumatoid Arthritis
3.5.5. Connective Tissue Tumors

3.5.5.1. Fribroma
3.5.5.2. Angioma

3.6. Maxillary and Mandibular Pathology

3.6.1. Features
3.6.2. Agnatia
3.6.3. Macrognatia
3.6.4. Micrognatia
3.6.5. Cleft Palate
3.6.6. Asymmetries
3.6.7. Treatment

3.7. Labial Pathology

3.7.1. Features
3.7.2. Fistulas and Labial Pits
3.7.3. Harelip
3.7.4. Morsicatio Buccarum
3.7.5. Cheilitis

3.7.5.1. Q. Simple
3.7.5.2. Q. Actinic
3.7.5.3. Allergic Contact Cheilitis
3.7.5.4. Q. Glandular
3.7.5.5. Q. Exfoliable
3.7.5.6. Q. Granulomatous
3.7.5.7. Macroqueilitis

3.7.6. Peutz Jeghers Syndrome
3.7.7. Mucocele
3.7.8. Tumors and Pseudotumors

3.8. Lingual Pathology

3.8.1. Features
3.8.2. Hair Removal
3.8.3. Saburral Tongue
3.8.4. Macroglossia
3.8.5. Ankyloglossia
3.8.6. Median Rhomboidal Glossitis
3.8.7. Hairy Tongue
3.8.8. Scrotal Tongue
3.8.9. Lingual Varicosities
3.8.10. Migratory Glossitis
3.7.11. Geographic Tongue
3.8.12. Cleft Tongue
3.8.13. Forked Tongue
3.8.14. Tumours
3.8.15. Motor Disturbances
3.8.16. Sensory Alterations

3.9. Vesicular-Ampholytic Diseases

3.9.1. Features and Types
3.9.2. Pemphigus

3.9.2.1. Vulgar
3.9.2.2. Erythematous
3.9.2.3. Foliaceous
3.9.2.4. Vegetant
3.9.2.5. Paraneoplastic

3.9.3. Pemphigoid

3.9.3.1. Cicatricial
3.9.3.2. Blistered

3.9.4. Linear IgA Dermatosis

3.9.4.1. Infant
3.9.4.2. Adults

3.9.5. Exudative Erythema Multiforme

3.9.5.1. Features
3.9.5.2. Etiology and Predisposing Factors
3.9.5.3. Sevens-Johnson Syndrome
3.9.5.4. Toxic Epidermal Necrolysis
3.9.5.5. Evolution, Prognosis and Treatment

3.9.6. Recurrent Aphthous Stomatitis (RAS)

3.9.6.1. Features
3.9.6.2. Etiology and Predisposing Factors
3.9.6.3. Major RAS
3.9.6.4. Minor RAS
3.9.6.5. Herpetiform Aphthous Stomatitis
3.9.6.6. Treatment

3.9.7. Associated Pathology and Syndromes

3.9.7.1. Celiac Disease
3.9.7.2. Crohn's Disease
3.9.7.3. Neutropenia
3.9.7.4. Behçet's Disease

3.10. Oral Lichen Planus

3.10.1. Etiology
3.10.2. Classification

3.10.2.1. Papular
3.10.2.2. Reticular
3.10.2.3. Atrophic
3.10.2.4. Erosive
3.10.2.5. Blistered
3.10.2.6. In Plaque
3.10.2.7. Others

3.10.3. Diagnosis
3.10.4. Treatment
3.10.5. Dermatitis Herpetiformis

3.11. Nutritional Alterations

3.11.1. Metabolic Alterations

3.11.1.1. Amyloidosis
3.11.1.2. Lipoid Proteinosis
3.11.1.3. Fabry Disease

3.11.2. Vit A
3.11.3. Vit B2
3.11.4. Vit B3
3.11.5. Vit C
3.11.6. Folic Acid
3.11.7. Zinc

Module 4. Special Patients: the Relationship between Systemic Diseases and Oral Pathology

4.1. Hematologic Alterations

4.1.1. Introduction
4.1.2. Red Series Diseases

4.1.2.1. Anaemia
4.1.2.2. Polyglobulia

4.1.3. White Series Diseases

4.1.3.1. Transplant Recipients: Before and After
4.1.3.2. HIV
4.1.3.3. Oncology Patients
4.1.3.4. Immunosuppressive Therapy for Autoimmune Pathology

4.1.4. Coagulation Alterations

4.1.4.1. Pharmacological anticoagulants
4.1.4.2. Haemophilia
4.1.4.3. Secondary to Other Pathologies

4.1.5. Langerhans Cell Histiocystosis

4.2. Endocrine Disorders

4.2.1. Introduction
4.2.2. Glands and Organs

4.2.2.1. Adrenal Gland
4.2.2.2. Pancreas
4.2.2.3. Kidneys
4.2.2.4. Brain
4.2.2.5. Genital System

4.2.3. Endocrine-Metabolic Pathology
4.2.4. Dialysis
4.2.5. Adrenal Insufficiency

4.2.5.1. Primary: Addison Disease
4.2.5.2. Secondary

4.2.6. Diabetes Mellitus

4.2.6.1. Types
4.2.6.2. Protocol
4.2.6.3. Hemochromatosis or Bronzed Diabetes

4.2.7. Thyroid Pathology

4.2.7.1. Hyperthyroidism
4.2.7.2. Hypothyroidism
4.2.7.3. Tumours

4.3. Digestive Alterations

4.3.1. Anatomy
4.3.2. Crohn's Disease
4.3.3. Ulcerative Colitis
4.3.4. Gastroesophageal Reflux
4.3.5. Hepatopathy or Liver Disease
4.3.6. Uremic Stomatitis
4.3.7. Related Oral Pathology and Treatment
4.3.8. Prevention

4.4. Pulmonary Alterations

4.4.1. Anatomy
4.4.2. Types and Diagnostic Tests
4.4.3. COPD
4.4.4. Wegner Disease
4.4.5. Sarcoidosis
4.4.6. Related Oral Pathology
4.4.7. Action Protocol

4.5. Cardiovascular Problems

4.5.1. Circulatory System
4.5.2. Valvulopathies
4.5.3. Cardiomyopathies
4.5.4. Pericardiopathies
4.5.5. Diseases of the Aorta
4.5.6. Hypertension
4.5.7. Action Protocol

4.5.7.1. Antibiotic Prophylaxis
4.5.7.2. Anesthesia

4.6. Neurological Alterations:

4.6.1. Nervous system

4.6.1.1. Central
4.6.1.2. Peripheral

4.6.2. Cerebrovascular Diseases
4.6.3. Cerebrovascular Accidents

4.6.3.1. Hemorrhagic
4.6.3.2. Ischemic

4.6.4. Epilepsy
4.6.5. Related Oral Pathology
4.6.6. Prevention
4.6.7. Action Protocol

4.7. Dependent Patients

4.7.1. Types
4.7.2. Geriatric Patient
4.7.3. Addicted Patients

4.7.3.1. Tobacco
4.7.3.2. Alcohol
4.7.3.3. Drugs
4.7.3.4. Drugs:
4.7.3.5. Unhealthy Habits

4.7.4. Disability

4.7.4.1. Intellectual
4.7.4.2. Sensory
4.7.4.3. Motor

4.7.5. Related Oral Pathology
4.7.6. Prevention
4.7.7. Action Protocol

4.8. Pregnancy

4.8.1. Definition
4.8.2. Nursing
4.8.3. Related Oral Pathology

4.8.3.1. Gingivitis
4.8.3.2. Pyogenic Granuloma
4.8.3.3. Cavities
4.8.3.4. Periodontal Disease

4.8.4. Dental Emergencies
4.8.5. Prevention
4.8.6. Action Protocol

4.9. Emergencias

4.9.1. Cognitive Alterations
4.9.2. Respiratory Alterations
4.9.3. Cardiac alterations
4.9.4. Allergies
4.9.5. Thoracic or Abdominal Pain
4.9.6. Anaphylactic Shock
4.9.7. Action Protocol

4.10. Oncology Patients

4.10.1. Definition
4.10.2. Types of Treatment

4.10.2.1. Radiotherapy
4.10.2.2. Chemotherapy
4.10.2.3. Brachytherapy
4.10.2.4. Surgical

4.10.3. Oncologic Treatment Phases
4.10.4. Related Oral Pathology
4.10.5. Prevention
4.10.6. Action Protocol

Module 5. Salivary Gland and TMJ Pathology

5.1. Saliva and anatomy of Gl. Gland Anatomy

5.1.1. Composition
5.1.2. Functions
5.1.3. Saliva Flow Variations
5.1.4. Applications and Diagnostic Use
5.1.5. Salivary Gland Anatomy Recap

5.1.5.1. Parótida
5.1.5.2. Sublingual
5.1.5.3. Submaxillary
5.1.5.4. Gl. Minor or accessory salivary glands

5.2. Gl malformations. Malformation and Pathologies

5.2.1. Exploration
5.2.2. Fistulas
5.2.3. Stafne Cavity
5.2.4. Pathologies and Causes
5.2.5. Diagnostic Tests

5.2.5.1. Radiological Diagnosis
5.2.5.2. Sialography Uses
5.2.5.3. Gammagraphy Uses

5.2.6. Complementary Tests
5.2.7. Serologic Test

5.3. Sialoadenitis

5.3.1. Features
5.3.2. Pathologies

5.3.2.1. Bacterial Suppurative
5.3.2.2. Viral

5.3.2.2.1. Epidemic Mumps
5.3.2.2.2. Cytomegalic Mumps

5.3.3. Chronicle

5.3.3.1. Bacterial

5.3.3.1.1. Tuberculous
5.3.3.1.2. Actinomycosis
5.3.3.1.3. Syphilitic

5.3.3.2. Allergic/toxic
5.3.3.3. Post Radiotherapy
5.3.3.4. Sclerosant
5.3.3.5. Recurrent (Juvenile)

5.4. Sialolithiasis

5.4.1. Features
5.4.2. Types

5.4.2.1. Pathologies
5.4.2.2. Chronicle

5.4.3. Mucocele
5.4.4. Garel's Hernia
5.4.5. Salivary Colic
5.4.6. Sialodochitis
5.4.7. Cannula
5.4.8. Treatment

5.5. Sialoadenosis

5.5.1. Features
5.5.2. Sarcoidosis
5.5.3. Cystic Fibrosis
5.5.4. Sd Sjögren

5.6. Tumor Pathology and Other Involvements

5.6.1. Features
5.6.2. Retention Cysts
5.6.3. Tumours
5.6.4. Sd Frey
5.6.5. Necrotizing Sialometaplasia

5.7. TMJ Anatomy

5.7.1. Bone Anatomy
5.7.2. Muscular Anatomy
5.7.3. Ligaments
5.7.4. Buttresses
5.7.5. Disks

5.8. TMJ Etiopathogenesis

5.8.1. Endocrine/Rheumatic Factors
5.8.2. Trauma
5.8.3. Psychosocial Factors

5.9. Pathologies. Classification

5.9.1. Congenital and Developmental Disorders
5.9.2. Condylar Pathology
5.9.3. Masticatory Muscle Disorders
5.9.4. Bone Pathology

5.9.4.1. Ankylosis
5.9.4.2. Arthritis

5.9.5. Tumorous Pathology

5.10. Exploration and Treatment

5.10.1. Clinical Examination
5.10.2. Diagnostic Tests

5.10.2.1. Ultrasound
5.10.2.2. Arthroscopy
5.10.2.3. Resonance
5.10.2.4. CAT
5.10.2.5. Open Mouth/Closed Mouth X-ray
5.10.2.6. Osteoprotegerin (OPG)

5.10.3. Treatment

5.10.3.1. Unloading Splint
5.10.3.2. Occlusal Adjustment

5.10.3.2.1. Selective Grinding
5.10.3.2.2. Orthodontics

5.10.3.3. Pharmacological
5.10.3.4. Botulinum toxin
5.10.3.5. Physiotherapy
5.10.3.6. Surgical

Module 6. Bone Lesions and Maxillary Cysts

6.1. General Information on Bone Tissue

6.1.1. Bone Tissue and Histology
6.1.2. Transformation and Remodeling

6.1.2.1. Systemic Factors
6.1.2.2. Local Factors

6.1.3. Concepts and Terminology

6.1.3.1. Hyperplasia
6.1.3.2. Dysplasia
6.1.3.3. Neoplasty

6.2. Etiopathogenesis and Classification

6.2.1. Classification
6.2.2. Predisposing Factors
6.2.3. Etiology
6.2.4. Diagnostic Tests

6.3. Bone Pathology

6.3.1. Osteoporosis
6.3.2. Osteomalacia
6.3.4. Osteoclerosis
6.3.5. Fibrous Dysplasia
6.3.6. Parathyroid Osteosis
6.3.7. Lymphomas
6.3.8. Myelomas

6.4. Maxillary Bone Infections

6.4.1. Periodontitis
6.4.2. Cellulite

6.4.2.1. Pathologies
6.4.2.1. Chronic

6.4.3. Fistulas

6.4.3.1. Acquired
6.4.3.2. Chronic

6.4.4. Osteitis
6.4.5. Osteomyelitis
6.4.6. Osteoperiostitis

6.5. Other Bone Pathologies

6.5.1. Osteogenesis Imperfecta
6.5.2. Osteonecrosis
6.5.3. Osteoradionecrosis
6.5.4. Bisphosphonates

6.5.4.1. Features
6.5.4.2. Clinical Management

6.6. Developmental Epithelial Odontogenic Cysts

6.6.1. Infant Gingival Cyst or Epstein Pearls
6.6.2. Primordial Cyst
6.6.3. Dentigerous or Follicular Cyst
6.6.4. Eruption Cyst
6.6.5. Lateral Periodontal Cyst
6.6.6. Adult Gingival Cyst
6.6.7. Glandular Odontogenic Cyst
6.6.8. Odontogenic Keratocyst

6.7. Non-Odontogenic Developmental Epithelial Cysts

6.7.1. Nasopalatine Duct Cyst
6.7.2. Nasolabial Cyst
6.7.3. Globulomaxillary Cyst
6.7.4. Median Alverolary, Palatine and Mandibular Cysts
6.7.5. Differential Diagnosis

6.8. Inflammatory Epithelial Cysts

6.8.1. Radicular Cyst

6.8.1.1. Apical and Lateral Cyst
6.8.1.2. Residual Cyst

6.8.2. Paradental Cyst
6.8.3. Differential Diagnosis

6.9. Non-Neoplastic Bone Lesions or Pseudocysts

6.9.1. Solitary Bone Cyst
6.9.2. Aneurysmal Bone Cyst
6.9.3. Differential Diagnosis

6.10. Osteofibrous Diseases

6.10.1. Maxillary Fibrous Dysplasia
6.10.2. Bone Cement Dysplasias

6.10.2.1. Periapical Cement Dysplasia
6.10.2.2. Florid Cemento-Osseous Dysplasia

6.10.3. Cherubism
6.10.4. Giant Cell Central Granuloma
6.10.5. Albright Syndrome
6.10.6. Paget’s Disease
6.10.7. Caffey’s Disease
6.10.8. Histiocytosis X
6.10.9. Basocellular or Gorlin's Nevus Syndrome
6.10.10. Ostogenic Neoplasms

Module 7. Benign Tumors

7.1. Etiopathogenesis and Classification

7.1.1. Histology
7.1.2. Classification
7.1.3. Predisposing Factors
7.1.4. Etiology

7.2. Connective Tissue and Muscular Tumors

7.2.1. Features
7.2.2. Fibroma
7.2.3. Myxoma
7.2.4. Xanthoma Verruciformis
7.2.5. Nodular Fascitis
7.2.6. Fibrous Hyperplasia
7.2.7. Tuberosity Bilateral Fibrous Hyperplasia
7.2.8. Fibrous Gingival Epulis
7.2.9. Cracked Epulis
7.2.10. Peripheral Giant Cell Granuloma (PGCG)
7.2.11. Leioma
7.2.12. Rhabdomyomas
7.2.13. Treatment

7.3. Vascular Tumours

7.3.1. Features
7.3.2. Hemangioma
7.3.3. Lymphangioma
7.3.4. Hemangioendothelioma
7.3.5. Features
7.3.6. Hemangiopericytoma
7.3.7. Glomus tumour
7.3.8. Pyogenic Granuloma
7.3.9. Pregnancy Epulis
7.3.10. Action Protocol

7.4. Neurogenic Tumors

7.4.1. Features
7.4.2. Neuromas

7.4.2.1. Traumatic
7.4.2.2. Neurofibromas
7.4.2.3. Von Recklinghausen Disease

7.4.3. Neurofibromas
7.4.4. Scwhannoma
7.4.5. Action Protocol

7.5. Adipose Lineage Tumors

7.5.1. Features
7.5.2. Lipoma
7.5.3. Fordyce Granules
7.5.4. Superficial Abscesses
7.5.5. Differential Diagnosis
7.5.6. Treatment

7.6. Osteoforming Tumors

7.6.1. Torus

7.6.1.1. Mandibular
7.6.1.2. Palatal

7.6.2. Central and Peripheral Osteoma
7.6.3. Osteoma Osteoid
7.6.4. Osteoblastoma
7.6.5. Chondroma
7.6.6. Osteochondroma
7.6.7. Condroblastoma
7.6.8. Ossifying Fibroma

7.7. Non-Osteoforming Tumors

7.7.1. Fibrous Tumors

7.7.1.1. Non-Specific Fibroma
7.7.1.2. Chondromyxoid Fibroma
7.7.1.3. Desmoplastic Fibroma

7.7.2. Giant Cell Tumor

7.7.2.1. PGCG
7.7.2.2. Giant Cell Tumor

7.8. Ectomesenchymal with or without Odontogenic Epithelium Inclusion

7.8.1. Odontogenic Fibroma
7.8.2. Myxoma
7.8.3. Benign Cementoblastoma
7.8.4. Cement-Ossifying Fibroma

7.9. Benign Odontogenic Tumors of Odontogenic Epithelium without Odontogenic Ectomesenchyma

7.9.1. Ameloblastomas
7.9.2. Calcifying Odontogenic Tumor or Pindborgs Tumor
7.9.3. Adenomatoid Squamous
7.9.4. Adenomatoid OT
7.9.5. Keratocystic TO

7.10. Benign Odontogenic Tumors of Odontogenic Epithelium with Odontogenic Ectomesenchyma

7.10.1. Ameloblastic Fibroma
7.10.2. Ameloblastic Fibrodentinoma (Dentinoma)
7.10.3. Odontoameloblastoma
7.10.4. Adenomatoid Odontogenic Tumor
7.10.5. Calcifying Odontogenic Tumor
7.10.6. Complex and Composite Odontoma
7.10.7. Calcifying Odontogenic Cystic Cystic Tumor or Gorlin's cyst

Module 8. White and Premalignant Lesions

8.1. White Leions

8.1.1. Classification

8.1.1.1. Hereditary Disorders
8.1.1.2. Reactive Lesions
8.1.1.3. Immunological Basis
8.1.1.4. Infectious Origin
8.1.1.5. Miscellaneous

8.1.2. Clinical Management

8.2. Premalignant Lesions

8.2.1. Concept of Premalignant Lesion
8.2.2. Histological Level
8.2.3. Classification
8.2.4. Predisposing Factors to Malignancy
8.2.5. Clinical Management

8.3. Leukoplakia

8.3.1. Features
8.3.2. Predisposing Factors
8.3.3. Etiology
8.3.4. Localisation
8.3.5. Types

8.3.5.1. Homogeneous
8.3.5.2. Non-Homogeneous

8.3.5.2.1. Erythroleukoplakia
8.3.5.2.2. Nodular
8.3.5.2.3. Exophytic

8.3.5.2.3.1. Verrucose
8.3.5.2.3.2. Proliferative Verrucosa

8.3.6. Pathological Anatomy

8.3.6.1. Stages
8.3.6.2. Dysplasia

8.3.7. Diagnosis
8.3.8. Treatment
8.3.9. Prognosis

8.4. Erythroplakia

8.4.1. Features
8.4.2. Predisposing Factors
8.4.3. Etiology
8.4.4. Localisation
8.4.5. Types

8.4.5.1. Homogeneous
8.4.5.2. Non-Homogeneous
8.4.5.3. Erythroleukoplakia

8.4.6. Diagnosis
8.4.7. Treatment
8.4.8. Prognosis

8.5. Actinic Cheilitis

8.5.1. Features
8.5.2. Predisposing Factors
8.5.3. Etiology
8.5.4. Treatment
8.5.5. Prognosis

8.6. Melanic Alterations

8.6.1. Features
8.6.2. Etiology
8.6.3. Diagnosis
8.6.4. Nevi
8.6.5. Pigmentary Nevus

8.6.5.1. Lentigo
8.6.5.2. Nevus Nevocyticus
8.6.5.3. Acquired Melanocytic Nevi

8.6.5.3.1. Junctional or Union Nevus
8.6.5.3.2. Compound Nevus
8.6.5.3.3. Intradermal Nevus

8.6.6. Organoid Nevus

8.6.6.1. Epithelial
8.6.6.2. Conjunctive
8.6.6.3. Vascular

8.6.7. Prevention
8.6.8. Treatment

8.7. Submucosal Oral Fibrosis

8.7.1. Features
8.7.2. Predisposing Factors
8.7.3. Etiology
8.7.4. Treatment

8.8. Xeroderma Pigmentosum

8.8.1. Features
8.8.2. Predisposing Factors
8.8.3. Etiology
8.8.4. Treatment

8.9. Plummer Vilson Disease

8.9.1. Features
8.9.2. Predisposing Factors
8.9.3. Etiology
8.9.4. Treatment

8.10. Dyskeratosis Congenita

8.10.1. Features
8.10.2. Predisposing Factors
8.10.3. Etiology
8.10.4. Treatment

8.11. Epidermolysis Bullosa

8.11.1. Features
8.11.2. Predisposing Factors
8.11.3. Etiology
8.11.4. Treatment

Module 9. Oral Cancer and Malignant Tumors

9.1. Etiopathogenesis and Classification

9.1.1. Histology
9.1.2. Classification
9.1.3. Predisposing Factors
9.1.4. Etiology
9.1.5. Prevalence

9.2. Malignant Odontogenic Tumors: Odontogenic Carcinomas

9.2.1. Malignant Ameloblastoma
9.2.2. Primary Intraosseous Carcinoma
9.2.3. Sclerosing Odontogenic Carcinoma
9.2.4. Clear Cell OC
9.2.5. Ghost Cell OC
9.2.6. Odontogenic Cysts Presenting Malignant Changes

9.3. Malignant Odontogenic Tumors: Odontogenic Sarcomas 

9.3.1. Ameloblastic Fibrosarcoma 
9.3.2. Ameloblastic Fibrodentinosarcoma and Ameloblastic Fibroodontosarcoma 
9.3.3. Odontogenic Carcinosarcoma 

9.4. Squamous Cell Oral Carcinoma

9.4.1. Features
9.4.2. Etiology
9.4.3. Histology
9.4.4. Diagnosis
9.4.5. Prevention
9.4.6. Treatment
9.4.7. Prognosis
9.4.8. Evolution

9.5. Verrucous Carcinoma

9.5.1. Features
9.5.2. Etiology
9.5.3. Diagnosis
9.5.4. Prevention
9.5.5. Treatment
9.5.6. Prognosis
9.5.7. Evolution

9.6. Adenocarcinoma

9.6.1. Features
9.6.2. Etiology
9.6.3. Diagnosis
9.6.4. Classification and Types
9.6.5. Prevention
9.6.6. Treatment
9.6.7. Prognosis
9.6.8. Evolution

9.7. Oral Melanoma

9.7.1. Features
9.7.2. Classification
9.7.3. Etiology
9.7.4. Diagnosis
9.7.5. Prevention
9.7.6. Treatment
9.7.7. Prognosis
9.7.8. Evolution

9.8. Lymphatic Disorders

9.8.1. Features
9.8.2. Etiology
9.8.3. Diagnosis
9.8.4. Classification and Types
9.8.5. Prevention
9.8.6. Treatment
9.8.7. Prognosis
9.8.8. Evolution

9.9. Sarcomas

9.9.1. Features
9.9.2. Etiology
9.9.3. Diagnosis
9.9.4. Classification and Types
9.9.5. Prevention
9.9.6. Treatment
9.9.7. Prognosis
9.9.8. Evolution

9.10. Minor Salivary Gland Neoplasms

9.10.1. Features
9.10.2. Etiology
9.10.3. Diagnosis
9.10.4. Prevention
9.10.5. Treatment
9.10.6. Prognosis
9.10.7. Evolution

Module 10. Neuropathologies

10.1. Features
10.2. Origin

10.2.1. Lobes and Involvements
10.2.2. Function Alterations
10.2.3. Predisposing Factors
10.2.4. Etiology

10.3. Pain

10.3.1. Nomenclature
10.3.2. Nerve fibers

10.3.2.1. Types
10.3.2.2. Neurotransmitters

10.3.3. Pathophysiology of Pain
10.3.4. Types of Pain
10.3.5. Treatment

10.4. Neuralgia

10.4.1. Definition
10.4.2. Types
10.4.3. Classification
10.4.4. Cranial Nerves
10.4.5. Spinal Nerves
10.4.6. Diagnosis
10.4.7. Treatment
10.4.8. Others

10.4.8.1. Facial Hemiatrophy
10.4.8.2. Minor Neuralgia
10.4.8.3. Fibromyalgia
10.4.8.4. Myofascial Pain

10.5. Trigeminal Neuralgia

10.5.1. Features
10.5.2. Origin
10.5.3. Predisposing Factors
10.5.4. Etiology
10.5.5. Diagnosis
10.5.6. Treatment
10.5.7. Evolution

10.6. Glossopharyngeal Neuralgia

10.6.1. Features
10.6.2. Origin
10.6.3. Predisposing Factors
10.6.4. Etiology
10.6.5. Diagnosis
10.6.6. Treatment
10.6.7. Evolution

10.7. Headaches and Cephalalgias

10.7.1. Clinical Classification
10.7.2. Pathophysiology
10.7.3. Migraines. Vascular Algias
10.7.4. Cluster Headache
10.7.5. Other Orofacial Pain

10.7.5.1. Burning Mouth Syndrome
10.7.5.2. Atypical Facial Algia
10.7.5.3. Hamulus Pterygoides Syndrome
10.7.5.4. Pterygoid Process Syndrome

10.7.6. Palliative Techniques for Pain

10.8. Burning Mouth Syndrome

10.8.1. Features
10.8.2. Origin
10.8.3. Predisposing Factors
10.8.4. Etiology
10.8.5. Diagnosis
10.8.6. Treatment
10.8.7. Evolution

10.9. Facial Paralysis

10.9.1. Etiology

10.9.1.1. Pathology
10.9.1.2. Traumatic
10.9.1.3. Congenital
10.9.1.4. Idiopathic
10.9.1.5. Yatrogenic

10.9.2. Types

10.9.2.1. Central Facial Paralysis
10.9.2.2. Peripheral Facial Paralysis

10.9.3. Treatment
10.9.4. Miscellaneous

10.9.4.1. Guillén-Barré Syndrome
10.9.4.2. Paget’s Disease
10.9.4.3. Melkersson-Rosenthal Syndrome
10.9.4.4. Myofascial Syndrome
10.9.4.5. Lupus
10.9.4.6. ALS
10.9.4.7. Diabetic Neuropathy

10.10. Bell’s Palsy

10.10.1. Features
10.10.2. Origin
10.10.3. Predisposing Factors
10.10.4. Etiology
10.10.5. Diagnosis
10.10.6. Treatment
10.10.7. Evolution

10.11. Ramsay Hunt Syndrome

10.11.1. Features
10.11.2. Origin
10.11.3. Predisposing Factors
10.11.4. Etiology
10.11.5. Diagnosis
10.11.6. Treatment
10.11.7. Evolution

This program will allow you to integrate the latest advances in Oral Medicine into your daily practice, giving you the opportunity to offer new services to your patients and users"