Diseases of the Mouth
Primary Oral Disease
Recurrent Aphthous Stomatitis (RAS)
RAS, also known as canker sores, is a common condition resulting in recurrent episodes of painful oral ulcers. It is important to consider other differentials which may be causing oral ulcers (e.g., Behçet’s disease, IBD, HIV, coeliac disease) before coming to a diagnosis of RAS.
Oral Squamous Cell Carcinoma (SCC)
SSC is responsible for the majority of tumours found in the mouth. Certain pre-cancerous lesions can predispose to SSC, such as leukoplakia, erythroplakia and lichen planus. Risk factors are tobacco (including oral tobacco products), excess alcohol, HPV (type 16), obesity, age, male sex, and poor nutrition.
Persistent unexplained oral ulcers or lumps should be referred for biopsy to rule out SCC.
Other Primary Oral Diseases
Geographic tongue ― recurrent idiopathic inflammatory disorder, which results in glossitis and patches of depapillation.
Black hairy tongue ― a benign condition which can be seen in smokers, those with poor oral hygiene and some antibiotics.
Leukoplakia ― white patches on the oral mucosa, which is very common. In some patients this may progress to SCC. This is not to be confused with oral hairy leukoplakia (caused by EBV), which is almost entirely seen in patients with HIV.
Erythroplakia ― presents as red patches in the oral mucosa. Erythroplakia is also a premalignant lesion with a high risk of progression to SCC. Surgical excision is a common treatment.
Secondary Oral Disease
Oral manifestations secondary to systemic diseases are often tested in the MRCP examinations. Some of the more common oral manifestations that are tested are summarised below (table 1).
| Speciality | Condition | Oral manifestations |
|---|---|---|
| Dermatology | Stevens-Johnson syndrome | Painful haemorrhagic erosions with a grey membrane |
| Autoimmune bullous disorders | Pemphigus vulgaris – oral mucosal ulceration is common | |
| Lichen planus | Wickham striae – fine white lines in the oral mucosa | |
| Angioedema | Hereditary angioedema caused by C1 esterase inhibitor deficiency. ACE inhibitors are a common trigger | |
| Haematology | Amyloidosis | Infiltration in the mouth – most commonly resulting in macroglossia |
| Leukaemia | Gingival hypertrophy (particularly in AML and APML) | |
| Endocrine | Addison’s disease | Hyperpigmentation – buccal mucosa, vermillion border, gums |
| Diabetes Mellitus | Gingivitis, periodontal disease | |
| Gastroenterology | Inflammatory Bowel Disease | Aphthous ulcers
Pyoderma vegetans – rare, pustules on the oral mucosa (more commonly seen in UC) |
| Coeliac disease | Enamel defects, mouth ulcers, atrophic glossitis | |
| Peutz-Jeghers syndrome | Hyperpigmented macules on the oral mucosa and lips | |
| Osler-Weber-Rendu syndrome (Hereditary Haemorrhagic Telangiectasia) | Telangiectasia can be seen around the mouth and face | |
| GORD | Acid erosion of the teeth | |
| Nutritional deficiencies | Angular cheilitis can be seen with iron/B12 deficiency | |
| Infectious Diseases | Oral candidiasis | White patches on the oral mucosa which can be scraped off leaving a raw area underneath. Caused by candida species |
| Oral hairy leukoplakia | Painless white plaques (typically on the lateral aspects of the tongue) which cannot be scraped off. Caused by EBV. | |
| Herpes Simplex Virus (HSV) | Cold sores
Herpetic gingivostomatitis can be seen in children who have not been exposed to HSV/immunosuppressed adults |
|
| Measles | Koplik’s spots are pathognomonic of measles infection (may precede rash) | |
| HIV seroconversion | Aphthous ulcers | |
| Kaposi’s sarcoma (KS) | Oral KS can be seen in patients with advanced HIV. It is associated with Human Herpesvirus-8 (HHV-8) | |
| Rheumatology | Behçet’s disease | Aphthous ulcers (genital ulcers also seen) |
| Systemic Lupus Erythematosus (SLE) | Aphthous ulcers, honeycomb plaques, non-specific erythema | |
| Genetic | Marfan’s syndrome | High-arched palate
Autosomal dominant mutation of FBN1 gene coding for fibrillin |
| Neurofibromatosis type 1 | Oral neurofibromas
Autosomal dominant mutation of NF-1 gene |
|
| Down’s syndrome | Macroglossia, crowded teeth
Trisomy 21 |
|
| Other | Radiotherapy | Oral mucositis |
Table 1: Secondary oral manifestations of systemic conditions
Gingival Hypertrophy and Macroglossia
The causes of gingival hypertrophy and macroglossia are frequently tested in the MRCP examinations. Causes of each are summarised below.
Gingival hypertrophy:
- Inflammatory enlargement
- Periodontal disease and poor dentition
- Drugs:
- Anticonvulsants e.g. phenytoin, lamotrigine
- Calcium-channel blockers (nifedipine in particular)
- Ciclosporin
- Neoplastic
- Leukaemia – particularly Acute Myeloblastic Leukaemia (AML)
- Infiltrative
- Granulomatosis with polyangiitis, sarcoidosis, amyloidosis
- Pregnancy
- Scurvy
Macroglossia
- Inherited
- Down syndrome
- Neurofibromatosis 1
- Mucopolysaccharidosis
- Glycogen storage disorders
- Acquired
- Endocrine
- Acromegaly
- Hypothyroidism
- Haematological
- Amyloidosis
- Lymphomas
- Multiple Myeloma
- Angioedema
- Carcinoma
- Endocrine
Oral Flora
The healthy oral cavity is polymicrobial and home to aerobic and anaerobic bacteria. As such, human bites resulting in skin and soft tissue infection are often polymicrobial in origin. This requires treatment with a broad-spectrum antibiotic such as co-amoxiclav. Transmission of blood-borne viruses such as HIV, hepatitis B and C can also occur if there has been blood exposure from a human bite.
Cat and dog bites, on the other hand, often isolate Pasteurella species. Infected cats may result in infection with Bartonella henselae, which causes ‘cat-scratch disease’ – a disease characterised by localised, painful lymphadenopathy.
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