Secondary Oral Disease | Medibuddy
15th July 2023

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

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