| Lichen planus |
|
Lichen planus affecting the shins.
|
| Classification and external resources |
| Specialty |
Dermatology |
| ICD-10 |
L43 |
| ICD-9-CM |
697.0 |
| DiseasesDB |
7452 |
| MedlinePlus |
000867 |
| eMedicine |
derm/233 derm/663 |
| Patient UK |
Lichen planus |
| MeSH |
D008010, D017676 |
Lichen planus (LP) is a disease of the skin and/or mucous membranes that resembles lichen. The cause is unknown, but it is thought to be the result of an autoimmune process with an unknown initial trigger. There is no cure, but many different medications and procedures have been used to control the symptoms.
The term lichenoid reaction (or lichenoid lesion) refers to a lesion of similar or identical histopathologic and clinical appearance to lichen planus (i.e. an area which looks the same as lichen planus, both to the naked eye and under a microscope).[1][2] Sometimes dental materials or certain medications can cause a lichenoid reaction.[1] They can also occur in association with graft versus host disease.[1][3]:258
Contents
- 1 Classification
- 1.1 Site
- 1.2 Pattern
- 1.3 Overlap syndromes
- 2 Signs and symptoms
- 2.1 Cutaneous lichen planus
- 2.2 Mucosal lichen planus
- 3 Causes
- 4 Diagnosis
- 4.1 Histopathology
- 4.2 Differential diagnosis
- 5 Treatment
- 5.1 Cutaneous lichen planus
- 5.2 Oral lichen planus
- 6 Prognosis
- 7 Epidemiology
- 8 History
- 9 Notes
- 10 References
- 11 External links
Classification
Lichen planus has been described as an autoimmune disease,[4] a dermatosis,[5] a papulosquamous disorder, a mucocutaneous disease,[6] and an inflammatory disease.[7]
Lichen planus lesions are so called because of their "lichen-like" appearance[8] and can be classified by the site they involve, or by their morphology.
Site
Lichen planus may be categorized as affecting mucosal or cutaneous surfaces.
- Cutaneous forms are those affecting the skin, scalp, and nails.[5][6][9]
- Mucosal forms are those affecting the lining of the gastrointestinal tract (mouth, pharynx, esophagus, stomach, anus), larynx, and other mucosal surfaces including the genitals, peritoneum, ears, nose, bladder and conjunctiva of the eyes.[7][10][11]
Pattern
Lichen planus lesions can occur in many different forms:
| Lesion morphology |
Description[12][13] |
| Annular |
'Ring-shaped' lesions that develop gradually from single small pigmented spots into circular groups of papules with clear, unaffected skin in the center. Annular lesions occur in approximately ten percent of lichen planus cases. The ring-like lesions may very slowly enlarge, co-join and morph into larger irregular (serpentine) bands, sometimes accompanied by lines (See Linear, below). |
| Linear |
Papules are arranged in a line (the "Blaschko line").[14] This pattern may develop secondary to trauma (koebnerization) or, uncommonly, as a spontaneous, isolated eruption, usually on the extremities, and rarely on the face.[15] |
| Hypertrophic |
This pattern usually occurs on the extremities, especially the shins and the interphalangeal joints, and tends to be the most pruritic variant of lichen planus. Also known as "Lichen planus verrucosus". |
| Atrophic |
This morphology is characterized by the presence of a few well-demarcated, white-bluish papules or plaques with central superficial atrophy. This is a rare variant of lichen planus. |
| Bullous |
This morphology is characterized by the development of vesicles and bullae with the skin lesions. This is a rare variant of lichen planus, and also known as "Vesiculobullous lichen planus". |
| Ulcerative |
This morphology is characterized by chronic, painful bullae and ulceration of the feet, often with cicatricial sequelae evident. This is a rare variant of lichen planus. |
| Pigmented |
This morphology is characterized by hyperpigmented, dark-brown macules in sun-exposed areas and flexural folds. This is a rare variant of lichen planus. |
Overlap syndromes
Occasionally, lichen planus is known to occur with other conditions. For example:
- Lupus erythematosus overlap syndrome. Lesions of this syndrome share features of both lupus erythematosus and lichen planus. Lesions are usually large and hypopigmented, atrophic, and with a red-to-blue colour and minimal scaling. Telangectasia may be present.[13][16]
- Lichen sclerosus overlap syndrome, sharing features of lichen planus and lichen sclerosus.[17]
Signs and symptoms
Lichen planus affecting the lower lip.
Although lichen planus can present with a variety of lesions, the most common presentation is as a well-defined area of purple-coloured, itchy, flat-topped papules with interspersed lacy white lines (Wickham's striae). This description is known as the characteristic "6 Ps" of lichen planus: planar (flat-topped), purple, polygonal, pruritic, papules, and plaques.[9] This rash, after regressing, is likely to leave an area of hyperpigmentation that slowly fades. That said, a variety of other lesions can also occur.[8]
Cutaneous lichen planus
Cutaneous lichen planus on the shin.
Lichen planus involving the nails.
Variants of cutaneous lichen planus are distinguished based upon the appearance of the lesions and/or their distribution.[18] Lesions can affect the:
- Extremities (face, dorsal hands, arms, and nape of neck).[a] This is more common in Middle Eastern countries in spring and summer, where sunlight appears to have a precipitating effect.[15][19][20]
- Palms and soles
- Intertriginous areas of the skin. This is also known as "Inverse lichen planus".[15]
- Nails[21] characterized by irregular longitudinal grooving and ridging of the nail plate, thinning of the nail plate, pterygium formation, shedding of the nail plate with atrophy of the nail bed, subungual keratosis, longitudinal erthronychia (red streaks), and subungual hyperpigmentation.[22] A sand-papered appearance is present in around 10% of individuals with nail lichen planus.[21]
- Scalp. This is also known as lichen planopilaris, acuminatus, follicular lichen planus, and peripilaris,[23] characterised by violaceous, scaly, pruritic papules. Scalp lichen planus can cause scarring alopecia if it is untreated.[9][20][24]
- Hair. This variant causes inflammation of hair follicles and gradual replacement with scarring. About 10% of people with lichen planus have the scalp or nail variants of the condition.[9]
Other variants may include:
- Lichen planus pemphigoides characterized by the development of tense blisters atop lesions of lichen planus or the development vesicles de novo on uninvolved skin.[25]
- Keratosis lichenoides chronica (also known as "Nekam's disease") is a rare dermatosis characterized by violaceous papular and nodular lesions, often arranged in a linear or reticulate pattern on the dorsal hands and feet, extremities, and buttock, and some cases manifests by sorrheic dermatitis like eruption on the scalp and face, also palmo plantar keratosis has been reported.[15][26][27]
- Lichenoid keratoses (also known as "Benign lichenoid keratosis," and "Solitary lichen planus"[15]) is a cutaneous condition characterized by brown to red scaling maculopapules, found on sun-exposed skin of extremities.[15][28] Restated, this is a cutaneous condition usually characterized by a solitary dusky-red to violaceous papular skin lesion.[29]
- Lichenoid dermatitis represents a wide range of cutaneous disorders characterized by lichen planus-like skin lesions.[15][28]
Mucosal lichen planus
Lichen planus on the lips and the lateral border of the tongue
Lichen planus affecting mucosal surfaces may have one lesion or be multifocal.[30] Examples of lichen planus affecting mucosal surfaces include:[30]
- Esophageal lichen planus, affecting the esophageal mucosa. This can present with difficulty or pain when swallowing due to oesophageal inflammation, or as the development of an esophageal stricture. It has also been hypothesized that it is a precursor to squamous cell carcinoma of the esophagus.[10][31]
- Genital lichen planus, which may cause lesions on the glans penis or skin of the scrotom in males, and the vulva or vagina in females.[9] Symptoms may include lower urinary tract symptoms associated with stenosis of the urethra, painful sexual intercourse, and itching.[9] In females, Vulvovaginal-gingival syndrome, is severe and distinct variant affecting the vulva, vagina, and gums, with complications including scarring, vaginal stricture formation,[32] or vulva destruction.[33] The corresponding syndrome in males, affecting the glans penis and gums, is the peno-gingival syndrome.[15] It is associated with HLA-DQB1.[15][34]
Oral lichen planus
Oral lichen planus (also termed oral mucosal lichen planus),[35] is a form of mucosal lichen planus, where lichen planus involves the oral mucosa, the lining of the mouth. This may occur in combination with other variants of lichen planus.[36] Six clinical forms of oral lichen planus are recognized:[36]
- Reticular, the most common presentation of oral lichen planus,[4] is characterised by the net-like or spider web-like appearance of lacy white lines, oral variants of Wickham's straiae.[36] This is usually asymptomatic.[4]
- Erosive/ulcerative, the second most common form of oral lichen planus,[4] is characterised by oral ulcers presenting with persistent, irregular areas of redness, ulcerations and erosions covered with a yellow slough. This can occur in one or more areas of the mouth. In 25% of people with erosive oral lichen planus, the gums are involved, described as desquamative gingivitis (a condition not unique to lichen planus). This may be the initial or only sign of the condition.[36]
- Papular, with white papules.
- Plaque-like appearing as a white patch which may resemble leukoplakia.[36]
- Atrophic, appearing as areas. Atrophic oral lichen planus may also manifest as desquamative gingivitis.[36]
- Bullous, appearing as fluid-filled vesicles which project from the surface.
These types often coexist in the same individual. Oral lichen planus tends to present bilaterally as mostly white lesions on the inner cheek,[4] although any mucosal site in the mouth may be involved. Other sites, in decreasing order of frequency, may include the tongue, lips, gingivae, floor of the mouth, and very rarely, the palate.[4]
Generally, oral lichen planus tends not to cause any discomfort or pain, although some people may experience soreness when eating or drinking acidic or spicy foodstuffs or beverages.[36] When symptoms arise, they are most commonly associated with the atrophic and ulcerative subtypes. These symptoms can include a burning sensation to severe pain.[4]
Causes
The cause of lichen planus is unknown,[8][34][37] but it is not contagious and does not involve any known pathogen.[38] It is thought to be a T cell mediated autoimmune reaction (where the body's immune system targets its own tissues).[4] This autoimmune process triggers apoptosis of the epithelial cells.[4] Several cytokines are involved in lichen planus, including tumor necrosis factor alpha, interferon gamma, interleukin-1 alpha, interleukin 6, and interleukin 8.[4] This autoimmune, T cell mediated, process is thought to be in response to some antigenic change in the oral mucosa, but a specific antigen has not been identified.[4]
Where a causal or triggering agent is identified, this is termed a lichenoid reaction rather than lichen planus. These may include:[11]
- Drug reactions, with the most common inducers including gold salts, beta blockers, traditional antimalarials (e.g. quinine), thiazide diuretics, furosemide, spironolactone, Metformin and penicillamine.[38]
- Reactions to amalgam (metal alloys) fillings (or when they are removed/replaced),[39]
- Graft-versus-host disease lesions, which chronic lichenoid lesions seen on the palms, soles, face and upper trunk after several months.[38]
- Hepatitis, specifically hepatitis B and hepatitis C infection, and primary biliary cirrhosis.[17][38]
It has been suggested that lichen planus may respond to stress, where lesions may present during times of stress. Lichen planus can be part of Grinspan's syndrome.[citation needed]
It has also been suggested that mercury exposure may contribute to lichen planus.[40]
Diagnosis
Lichen planus lesions are diagnosed clinically by their "lichen-like" appearance.[8] A biopsy can be used to rule out conditions that may resemble lichen planus, and can pick up any secondary malignancies.[41]
Histopathology
Micrograph of lichen planus. H&E stain.
Lichen planus has a unique microscopic appearance that is similar between cutaneous, mucosal and oral. A Periodic acid-Schiff stain of the biopsy may be used to visualise the specimen. Histological features seen include:[42]
- thickening of the stratum corneum both with nuclei present (parakeratosis) and without (orthokeratosis). Parakeratosis is more common in oral variants of lichen planus.
- thickening of the stratum granulosum
- thickening of the stratum spinosum (acanthosis) with formation of colloid bodies (also known as Civatte bodies, Sabouraud bodies) that may stretch down to the lamina propria.
- liquefactive degeneration of the stratum basale, with separation from the underlying lamina propria, as a result of desmosome loss, creating small spaces (Max Joseph spaces).
- Infiltration of T cells in a band-like pattern into the dermis[4] "hugging" the basal layer.
- Development of a "saw-tooth" appearance of the rete pegs, which is much more common in non-oral forms of lichen planus.
Differential diagnosis
The differential diagnosis for OLP includes:
- Other oral vesiculo-ulcerative conditions such as Pemphigus vulgaris and Benign mucous membrane pemphigoid
- Lupus erythematosus, with lesions more commonly occur on the palate and appear as centrally ulcerated or erythematous with radiating white striae. In contrast, OLP and lichenoid reactions rarely occur on the palate, and the striae are randomly arranged rather than radial.[43]
- Chronic ulcerative stomatitis
- Frictional keratosis and Morsicatio buccarum (chronic cheek biting)
- Oral leukoplakia
- Oral candidiasis
Treatment
There is no cure for lichen planus,[4] and so treatment of cutaneous and oral lichen planus is for symptomatic relief or due to cosmetic concerns.[4][8][41] When medical treatment is pursued, first-line treatment typically involves corticosteroids,[8] and removal of any triggers.[39] Without treatment, most lesions will spontaneously resolve within 6–9 months for cutaneous lesions,[8] and longer for mucosal lesions [42]
Cutaneous lichen planus
Many different treatments have been reported for cutaneous lichen planus, however there is a general lack of evidence of efficacy for any treatment.[14][44] Treatments tend to be prolonged, partially effective and disappointing.[14] First-line treatments may include retinoids such as Acitretin, or corticosteroids [8][14][44]
A variety of other therapies are also used if these are unsuccessful. These include oral corticosteroids, vitamin D3 analogues, antibiotics such as Dapsone, hydroxychloroquine and Cyclosporin, some anti-coagulants,[which?] and psoralen plus ultraviolet-A.[8][14][44]
Cosmetic treatments may include laser surgery, cryotherapy, and phototherapy.[14][44]
Oral lichen planus
Reassurance that the condition is benign, elimination of precipitating factors and improving oral hygiene are considered initial management for symptomatic OLP, and these measures are reported to be useful.[4] Treatment usually involves topical corticosteroids (such as betamethasone, clobetasol, dexamethasone, and triamcinolone) and analgesics, or if these are ineffective and the condition is severe, the systemic corticosteroids may be used. Calcineurin inhibitors (such as pimecrolimus, tacrolimus) or cyclosporin) are sometimes used.[4]
Prognosis
In contrast to cutaneous lichen planus, lichen planus lesions in the mouth may persist for many years,[41] and tend to be difficult to treat, with relapses being common.[34] Atrophic/erosive lichen planus is associated with a small risk of malignant transformation,[41] and so people with OLP tend to be kept on long term review to detect any potential change early. Sometimes OLP can become secondarily infected with Candida organisms.[citation needed]
Epidemiology
The overall prevalence of lichen planus in the general population is about 0.1 - 4%.[9] It generally occurs more commonly in females, in a ratio of 3:2, and most cases are diagnosed between the ages of 30 and 60, but it can occur at any age.[9][45]
Oral lichen planus is relatively common,[34] It is one of the most common mucosal diseases. The prevalence in the general population is about 1.27-2.0%,[4][41] and it occurs more commonly middle aged people.[4] OLP in children is rare. About 50% of females with oral lichen planus were reported to have undiagnosed vulvar lichen planus.[9]
History
Lichen planus was first reported in 1869 by Erasmus Wilson.[42]
Notes
- ^ Cutaneous lichen planus affecting the extremities is also known as "Lichen planus actinicus", "Actinic lichen niditus," "Lichen planus atrophicus annularis," "Lichen planus subtropicus," "Lichen planus tropicus," "Lichenoid melanodermatitis," and "Summertime actinic lichenoid eruption"
References
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- ^ Freedberg, Irwin M., ed. (2003). Fitzpatrick's dermatology in general medicine (6th ed.). New York, NY: McGraw-Hill. p. 466. ISBN 0-07-138076-0.
- ^ Freedberg, Irwin M., ed. (2003). Fitzpatrick's dermatology in general medicine (6th ed.). New York, NY: McGraw-Hill. p. 468. ISBN 0-07-138076-0.
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- ^ Freedberg, Irwin M., ed. (2003). Fitzpatrick's dermatology in general medicine (6th ed.). New York, NY: McGraw-Hill. p. 471. ISBN 0-07-138076-0.
- ^ Freedberg, Irwin M., ed. (2003). Fitzpatrick's dermatology in general medicine (6th ed.). New York, NY: McGraw-Hill. p. 472. ISBN 0-07-138076-0.
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External links
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Wikimedia Commons has media related to Lichen planus. |
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Papulosquamous disorders (L40–L45, 696–697)
|
|
| Psoriasis |
| Pustular |
- Generalized pustular psoriasis (Impetigo herpetiformis)
- Acropustulosis/Pustulosis palmaris et plantaris (Pustular bacterid)
- Annular pustular psoriasis
- Localized pustular psoriasis
|
|
| Other |
- Guttate psoriasis
- Psoriatic arthritis
- Psoriatic erythroderma
- Drug-induced psoriasis
- Inverse psoriasis
- Napkin psoriasis
- Seborrheic-like psoriasis
|
|
|
| Parapsoriasis |
- Pityriasis lichenoides (Pityriasis lichenoides et varioliformis acuta, Pityriasis lichenoides chronica)
- Lymphomatoid papulosis
- Small plaque parapsoriasis (Digitate dermatosis, Xanthoerythrodermia perstans)
- Large plaque parapsoriasis (Retiform parapsoriasis)
|
|
| Other pityriasis |
- Pityriasis rosea
- Pityriasis rubra pilaris
- Pityriasis rotunda
- Pityriasis amiantacea
|
|
| Other lichenoid |
| Lichen planus |
- configuration
- morphology
- Hypertrophic
- Atrophic
- Bullous
- Ulcerative
- Actinic
- Pigmented
- site
- Mucosal
- Nails
- Peno-ginival
- Vulvovaginal
- overlap synromes
- with lichen sclerosus
- with lupus erythematosis
- other:
- Hepatitis-associated lichen planus
- Lichen planus pemphigoides
|
|
| Other |
- Lichen nitidus
- Lichen striatus
- Lichen ruber moniliformis
- Gianotti–Crosti syndrome
- Erythema dyschromicum perstans
- Idiopathic eruptive macular pigmentation
- Keratosis lichenoides chronica
- Kraurosis vulvae
- Lichen sclerosus
- Lichenoid dermatitis
- Lichenoid reaction of graft-versus-host disease
|
|
|
|
Index of skin
|
|
| Description |
- Anatomy
- Physiology
- Development
|
|
| Disease |
- Infections
- Vesiculobullous
- Dermatitis and eczema
- Papulosquamous
- Urticaria and erythema
- Radiation-related
- Pigmentation
- Mucinoses
- Keratosis, ulcer, atrophy, and necrobiosis
- Vasculitis
- Fat
- Neutrophilic and eosinophilic
- Congenital
- Neoplasms and cancer
- nevi and melanomas
- epidermis
- dermis
- Symptoms and signs
- Terminology
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| Treatment |
- Procedures
- Drugs
- antibiotics
- disinfectants
- emollients and protectives
- itch
- psoriasis
- other
- Wound and ulcer
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Oral and maxillofacial pathology (K00–K06, K11–K14, 520–525, 527–529)
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Lips
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- Cheilitis
- Actinic
- Angular
- Plasma cell
- Cleft lip
- Congenital lip pit
- Eclabium
- Herpes labialis
- Macrocheilia
- Microcheilia
- Nasolabial cyst
- Sun poisoning
- Trumpeter's wart
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Tongue
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- Ankyloglossia
- Black hairy tongue
- Caviar tongue
- Crenated tongue
- Cunnilingus tongue
- Fissured tongue
- Foliate papillitis
- Glossitis
- Geographic tongue
- Median rhomboid glossitis
- Transient lingual papillitis
- Glossoptosis
- Hypoglossia
- Lingual thyroid
- Macroglossia
- Microglossia
- Rhabdomyoma
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Palate
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- Bednar's aphthae
- Cleft palate
- High-arched palate
- Palatal cysts of the newborn
- Inflammatory papillary hyperplasia
- Stomatitis nicotina
- Torus palatinus
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Oral mucosa - Lining of mouth
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- Amalgam tattoo
- Angina bullosa haemorrhagica
- Behçet syndrome
- Bohn's nodules
- Burning mouth syndrome
- Candidiasis
- Condyloma acuminatum
- Darier's disease
- Epulis fissuratum
- Erythema multiforme
- Erythroplakia
- Fibroma
- Focal epithelial hyperplasia
- Fordyce spots
- Hairy leukoplakia
- Hand, foot and mouth disease
- Hereditary benign intraepithelial dyskeratosis
- Herpangina
- Herpes zoster
- Intraoral dental sinus
- Leukoedema
- Leukoplakia
- Lichen planus
- Linea alba
- Lupus erythematosus
- Melanocytic nevus
- Melanocytic oral lesion
- Molluscum contagiosum
- Morsicatio buccarum
- Oral cancer
- Benign: Squamous cell papilloma
- Keratoacanthoma
- Malignant: Adenosquamous carcinoma
- Basaloid squamous carcinoma
- Mucosal melanoma
- Spindle cell carcinoma
- Squamous cell carcinoma
- Verrucous carcinoma
- Oral florid papillomatosis
- Oral melanosis
- Pemphigoid
- Pemphigus
- Plasmoacanthoma
- Stomatitis
- Aphthous
- Denture-related
- Herpetic
- Smokeless tobacco keratosis
- Submucous fibrosis
- Ulceration
- Verruca vulgaris
- Verruciform xanthoma
- White sponge nevus
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Teeth (pulp, dentin, enamel)
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- Amelogenesis imperfecta
- Ankylosis
- Anodontia
- Caries
- Concrescence
- Delayed eruption
- Dens evaginatus
- Dentin dysplasia
- Dentin hypersensitivity
- Dentinogenesis imperfecta
- Dilaceration
- Ectopic enamel
- Enamel hypocalcification
- Enamel hypoplasia
- Enamel pearl
- Fluorosis
- Fusion
- Gemination
- Hyperdontia
- Hypodontia
- Maxillary lateral incisor agenesis
- Impaction
- Macrodontia
- Meth mouth
- Microdontia
- Odontogenic tumors
- Keratocystic odontogenic tumour
- Odontoma
- Open contact
- Premature eruption
- Pulp calcification
- Pulp necrosis
- Pulp polyp
- Pulpitis
- Regional odontodysplasia
- Resorption
- Supernumerary root
- Taurodontism
- Trauma
- Avulsion
- Cracked tooth syndrome
- Vertical root fracture
- Occlusal
- Tooth loss
- Tooth wear
- Abrasion
- Abfraction
- Acid erosion
- Attrition
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Periodontium (gingiva, Periodontal ligament, cementum, alveolus) - Gums and tooth-supporting structures
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- Cementoblastoma
- Cementoma
- Eruption cyst
- Epulis
- Pyogenic granuloma
- Congenital epulis
- Gingival enlargement
- Gingival cyst of the adult
- Gingival cyst of the newborn
- Gingivitis
- Desquamative
- Granulomatous
- Plasma cell
- Hereditary gingival fibromatosis
- Hypercementosis
- Hypocementosis
- Linear gingival erythema
- Necrotizing periodontal diseases
- Acute necrotizing ulcerative gingivitis
- Pericoronitis
- Peri-implantitis
- Periodontal abscess
- Periodontal trauma
- Periodontitis
- Aggressive
- As a manifestation of systemic disease
- Chronic
- Perio-endo lesion
- Teething
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Periapaical, mandibular and maxillary hard tissues - Bones of jaws
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- Agnathia
- Alveolar osteitis
- Cherubism
- Idiopathic osteosclerosis
- Mandibular fracture
- Microgenia
- Micrognathia
- Intraosseous cysts
- Odontogenic: periapical
- Dentigerous
- Buccal bifurcation
- Lateral periodontal
- Globulomaxillary
- Calcifying odontogenic
- Glandular odontogenic
- Non-odontogenic: Nasopalatine duct
- Median mandibular
- Median palatal
- Traumatic bone
- Osteomyelitis
- Osteonecrosis
- Bisphosphonate-associated
- Neuralgia-inducing cavitational osteonecrosis
- Osteoradionecrosis
- Osteoporotic bone marrow defect
- Paget's disease of bone
- Periapical abscess
- Periapical periodontitis
- Stafne defect
- Torus mandibularis
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Temporomandibular joints, muscles of mastication and malocclusions - Jaw joints, chewing muscles and bite abnormalities
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- Bruxism
- Condylar resorption
- Mandibular dislocation
- Malocclusion
- Crossbite
- Open bite
- Overbite
- Overjet
- Prognathia
- Retrognathia
- Temporomandibular joint dysfunction
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Salivary glands
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- Benign lymphoepithelial lesion
- Ectopic salivary gland tissue
- Frey's syndrome
- HIV salivary gland disease
- Necrotizing sialometaplasia
- Mucocele
- Pneumoparotitis
- Salivary duct stricture
- Salivary gland aplasia
- Salivary gland atresia
- Salivary gland diverticulum
- Salivary gland fistula
- Salivary gland hyperplasia
- Salivary gland hypoplasia
- Salivary gland neoplasms
- Benign: Basal cell adenoma
- Canalicular adenoma
- Ductal papilloma
- Monomorphic adenoma
- Myoepithelioma
- Oncocytoma
- Papillary cystadenoma lymphomatosum
- Pleomorphic adenoma
- Sebaceous adenoma
- Malignant: Acinic cell carcinoma
- Adenocarcinoma
- Adenoid cystic carcinoma
- Carcinoma ex pleomorphic adenoma
- Lymphoma
- Mucoepidermoid carcinoma
- Sclerosing polycystic adenosis
- Sialadenitis
- Parotitis
- Chronic sclerosing sialadenitis
- Sialectasis
- Sialocele
- Sialodochitis
- Sialosis
- Sialolithiasis
- Sjögren's syndrome
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Orofacial soft tissues - Soft tissues around the mouth
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- Actinomycosis
- Angioedema
- Basal cell carcinoma
- Cutaneous sinus of dental origin
- Cystic hygroma
- Gnathophyma
- Ludwig's angina
- Macrostomia
- Melkersson–Rosenthal syndrome
- Microstomia
- Noma
- Oral Crohn's disease
- Orofacial granulomatosis
- Perioral dermatitis
- Pyostomatitis vegetans
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Other
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- Eagle syndrome
- Hemifacial hypertrophy
- Facial hemiatrophy
- Oral manifestations of systemic disease
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Index of the mouth
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| Description |
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| Disease |
- Congenital
- face and neck
- cleft
- digestive system
- Neoplasms and cancer
- Other
- Symptoms and signs
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| Treatment |
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