mouth_ulcers
Table of Contents
mouth ulcers
see also:
differential diagnoses
apthous ulcers
- also known as aphthous stomatitis
- oval or round ulcers usually on the inside of lips, cheeks or under the tongue where the mucosa is not tightly bound to underlying bone.
- may also appear on genitals if associated with Behcet disease or HIV.
- 40% have a FH
- often triggered by stress, menses or mechanical trauma (eg. accidental self bite of mucosa)
- perhaps one of the few conditions LESS prevalent in smokers!
- 80% are of the minor recurrent type
- higher incidence in those with coeliac disease
herpes simplex
- primary herpetic gingivostomatitis
- first exposure to Herpes simplex virus (HSV) may result in a widespread very painful ulcerated inflammation of oral mucosa, gums and tongue which usually lasts 10-14 days
- often occurs in pre-school children
- secondary recurrent HSV “cold sores”:
- the common “cold sore”
herpangina
- Coxsackie virus A infection resulting in ulceration of the posterior pharynx - usually on the soft palate.
- mainly children in Summer
hand, foot and mouth disease
- Coxsackie A virus infection - mainly an infection of pre-school children; may also be caused by Enterovirus 71.
- helpful diagnostic findings include:
- purple blistering of medial borders of feet/great toe and hands
- maculopapular rash over buttocks in infants
necrotising ulcerative gingivitis
periodic fever with aphthous stomatitis, pharyngitis and adenitis (PFAPA syndrome)
- recurrent febrile illness with aphthous stomatitis and adenitis starting in children aged 2-5yrs and becoming rare after age 10yrs
- sporadic and familial cases are rare
- periodicity of 3-6wks resembles cyclic neutropenia suggesting some common biologic clock mechanism
- fevers up to 41degC for 3-6 days, then suddenly fall to normal
- 40-70% develop aphthous ulcers
- most have tender cervical adenopathy and pharyngitis
- most have moderate neutrophilia and raised ESR
- striking response to single dose of corticosteroids
hyperimmunoglobulin D syndrome (HIDS)
- autosomal recessive periodic fever syndrome
- episodic attacks of fever lasting 3-7 days, usually accompanied by chills, cervical lymphadenopathy, abdominal pain, and vomiting or diarrhoea
- some experience headache, arthralgias or arthritis, aphthous ulceration, a pleomorphic rash, and, occasionally, splenomegaly
- 2/3rds begin in 1st year of life
- most have IgD >100 international units/mL
- 80% have elevated IgA
- raised ESR, CRP occur during attacks and may remain high between attacks
cyclic neutropenia
- characterised by a 14-35 day periodic cycle of neutropenia which may cause aphthous ulcers and gingivitis during attacks
lingual zoster
- vesicles present on only the left or the right side of the tongue with minimal crossing of the midline
- may be associated with features of Ramsay Hunt Syndrome:
- facial palsy, often mild
- otalgia
- vesicles in ear canal
- occasionally, hearing loss
Steven's Johnson syndrome
- life threatening, widespread blistering condition of the whole body with ulceration of oro-genital mucosa
neutropenic states
- mouth ulcers may be a sign of severe neutropenia
neoplasia
- chronic ulcerated lesions in the elderly should raise the suspicion of carcinoma of the oropharynx, or chronic irritation from poorly fitting dentures
leukoplakia
- white plaques rather than ulceration, often due to chronic inflammation due to dentures
- hairy leukoplakia is associated with EBV / glandular fever / infectious mononucleosis and occurs primarily in HIV-positive individuals.
Behcet's disease
- painful mouth ulcers are usually the first outward sign of Behcet disease and occur in about 70% of patients.
- ulcers can occur anywhere in the mouth including on the tongue and inside the lips and cheeks.
- usually last for 1-2 weeks but can remain for as long as 3 weeks.
- onset is usually between 30 and 40 years of age
- 1 in 10,000 from “Silk Road” ethnicities, 1 in 20,000 in Western ethnicities
- may be associated with genital ulcers, uveitis, erythema nodosum, tonsillitis, general constitutional symptoms
- see DermNetNZ
oral lichen planus
- mouth is involved in half of patients with lichen planus
- painless white streaks or fern-like pattern on buccal mucosa
- painful and persistent mouth ulcers (erosive lichen planus)
- desquamative gingivitis
- some cases are due to contact allergy to mercury amalgam dental fillings
- see dermnetnz
discoid lupus erythematosis
- usually mainly affects cheeks, nose, ears and sometimes light exposed areas (upper back, V neck, back of hands)
- it can cause mouth and lip ulcers, and these lesions may predispose to SCC
SLE
oral candidiasis
- white plaques rather than ulcers, but in the acute pseudomembranous form, these white patches can be peeled off to leave a raw area.
geographic tongue
- see DermNetNZ
angular cheilitis
- red, painful fissuring of the angle of the mouth
- may be due to:
- candida - eg. dentures, diabetes, steroids, antibiotic use
- Staph aureus
- HSV cold sores
- contact dermatitis from saliva due to constant dribbling or licking
- dry chapped lips from sun/wind/cold exposure
- poor nutrition - coeliac disease, iron deficiency, riboflavin deficiency
- inflammatory bowel disease
- sensitive skin - eg. atopic skin
- retinoid use - eg. isotretoin for acne, acitretin for psoriasis
- see DermNetNZ
mouth_ulcers.txt · Last modified: 2024/11/12 05:54 by gary1