lichen planus and lichenoid reactions Flashcards

1
Q

what is the definition of lichen planus?

A

> a clinically distinctive macupapular mucocutaneous rash with a characteristic distribution
itchy when affecting skin with a tendency to develop at sites of trauma
eventually heals without scar but may leave hyperpigmented macules

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2
Q

what is lichen planus like on the skin?

A

> violaceous papule topped with a silver scale
flexor aspect of wrists, forearms, ankles and also torso
wickhams striae present
oral and skin lichen planus have many Similarities but are not the same

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3
Q

what is a lichenoid reaction?

A

> something that resembles lichen planus clinically and histologically but is caused by an identifiable agent eg. a drug

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4
Q

what are the general features of LP?

A

affects around 2% of the population -
> half of those with skin LP have oral lesions
> not everyone with oral lesions have skin LP

> females more than males
rare in children generally older (40+) age group

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5
Q

what is the aetiology of oral LP?

A

UNKNOWN

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6
Q

what are the proposed aetiological factors?

A

> infective organ (viruses)
stress
autoimmunity
drug therapy
restorative material
idiopathic

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7
Q

when do you call LP a LR?

A

if you can determine that the changes are due to drug therapy, restorative materials or other triggers

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8
Q

what do you call a LR caused by a restorative agent?

A

> contact lesion

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9
Q

what is Idiopathic lichen planus?

A

> if you can’t determine that the changes are due to drug therapy, restorative materials or other triggers

(in a proportion of patients, careful analysis revealed possible causative agents the elimination of which is followed by healing of the lesions

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10
Q

what is the difference between LP and LR?

A

> develops 3 weeks after change in antihypertensive medication (= LR)
resolves when old amalgams replaced by composite (= LR)
no fillings, no drugs, PMH NAD (=LP)

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11
Q

what is the onset of LP and LR?

A

onset = spontaneous or related to any event?

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12
Q

what is the duration of LP and LR?

A

> duration = chronic, years rather than months

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13
Q

what is the number of LP and LR?

A

> number = usually multiple

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14
Q

what is the frequency of LP and LR?

A

> frequency = persistent, perhaps with episodic exacerbations

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15
Q

what are the sites of LP and Lr?

A

> sites = almost anywhere in the month , bilateral or unilateral?

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16
Q

what is the systemic upset of LP and LR?

A

systemic upset - none (minority have involvement of other mucosal or cutaneous sites)

17
Q

what are the presenting pathways of LP and LR?

A

> asymptomatic
discomfort/ pain on eating
change in texture of mucosa
ulceration

18
Q

what is the variety of clinical patterns LP/ LR can appear as?

A

> reticular
papular
plaque
atrophic
erosive
bullous

(you can have different patterns on the same patient)

19
Q

what are the most common sites of distribution?

A

> buccal mucosa
lateral border of tongue
dorsum of the tongue
attached gingiva

20
Q

what are the least common sites of LP/LR

A

> palate
floor of mouth
edentulous alveolar mucosa

21
Q

what are the other sites affected by LP/LR?

A

> skin
Nails
genitalia
ears (tympanic membrane
conjunctiva
oesophagus

22
Q

histopathology of LP/ LR ?

A

> epithelium may be hyperkeratonic, hyperplastic, atrophic or ulcerated
basal cell layer exhibits “liquefaction degeneration” (apoptosis, civatte bodies)
band like infiltrate of T Lympocytes hugging the interface, many lymphocytes trafficking through the epithelium
interface mucositis (umbrella term)

23
Q

what is the proposed pathogenesis of LP/ LR ?

A
  1. something alters the protein signature of the basal keratinocyte
  2. langerhans cells detect the new antigen
  3. antigen presented to T cells
  4. cell mediated immunity develops
  5. T cells infiltrate back to the altered epithelium and kill individual basal cells
  6. the epithelium reacts in the only way it knows
24
Q

what conditions mimic LP/LR?

A

> frictional keratosis
lupus erythematous
tobacco-related keratosis
potentially malignant oral lesion
graft versus- host disease

25
Q

what to do with LP/ LP?

A
  1. establish a diagnosis - exclude other conditions that can present in a similar way
  2. consider treatment (build up slowly)
  3. try to identify the cause and exclude it
  4. keep an eye on things
26
Q

how do you establish a diagnosis?

A
  1. history - HPC usually not informative, ask about tobacco, drugs and OTC medications
  2. Examinations - appearance, distributions, relationship to restorations
  3. special investigations - biopsy (not always required), other tests eg blood
27
Q

Treatment options for LP/ LR ?

A

> treatment is supportive, some cases resolve spontaneously, most patients are never cured

  1. no active treatment - review, observation
  2. topical steroids - pellets, mouthwash
  3. systemic steroids
  4. other immunomodulatory agents - topical or systemic