Pityriasis lichenoides Flashcards

1
Q

Both PLEVA and PLC are characterized by the clinical findings of:

A
  • recurrent crops of self-resolving lesions
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2
Q

Etiology of PLEVA/PLC?

A
  • unclear, may represent response to infections/drugs, or may represent low grade T-cell lymphoproliferative disorder
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3
Q

PLEVA has ____ onset of lesions .

A
  • rapid onset
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4
Q

Where does PLEVA tend to occur on body?

A
  • widespread (trunk, buttock, and proximal extremities> other sites)
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5
Q

Describe the primary lesions of PLEVA

A
  • pink papule that turn into vesicles, can necrose/become purpuric
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6
Q

How do lesions of PLEVA heal?

A
  • with varioliform scars! (Varioliformis)
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7
Q

_____ is a variant of PLEVA and presents with systemic systems including _____

A
  • Febrile ulceronecrotic Mucha-Haberman disease
  • FUMH has PLEVA
  • High fever, constitutional symptoms, LAD, arthritis, mucosal, pulmonary and GI involvement.
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8
Q

Febrile ulceronecrotic Mucha-Haberman disease (PLEVA variant) is a/w increased _____ levels

A
  • increased TNF alpha levels
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9
Q

Pityriasis lichenoides chronic presents with:

A
  • widespread, red-brown, scaly papule and plaques
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10
Q

PLC resolves with _____ whereas PLEVA resolves with ____

A
  • hypopigmentation

- varioliform scars

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11
Q

Which occurs more frequently in adults, PLC or PLEVA

A

PLC>PLEVA in adults (adults are chronic)

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12
Q

Histology of PLEVA:

A

PLEVA: P- Parakeratosis
L- Lichenoid infiltrate
E- Extravasation of RBC’s
V- V-shaped dermal lymphocytic infiltrate
A- Acute epidermal changes (dyskeratosis, ulceration, neutrophilic scale crust)

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13
Q

Histology of PLC:

A

similar to PLEVA, but MORE SUBTLE
P- Parakeratosis
L- Lichenoid infiltrate
E- Extravasation of RBC’s
V- V-shaped dermal lymphocytic infiltrate
A- Acute epidermal changes (dyskeratosis, ulceration, neutrophilic scale crust)

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14
Q

Histology of PLEVA and PLC both have strict absence of______.

What is another interface dermatitis that does not have these (in most subtypes)

A
  • eosinophils!!!!!!

- Lichen Planus does not have eos, unless its drug induced or hypertrophic forms

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15
Q

First line of tx for PLEVA and PLC

A
  • topical steroids, phototherapy, systemic antibiotics (erythromycin, azithromycin)
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16
Q

Severe forms of PLEVA/PLC can be treated with:

A
  • if severe, can use MTX, cyclosporine, and IVIG
17
Q

What is the best predictor for speed of disease resolution for PLEVA/PLC?

A
  • distribution of disease
18
Q

Which distribution of PLEVA/PLC resolves fastest, slowest, in between?

A
  • diffuse distribution resolves fastest (11 months on average)
  • slowest is peripheral distribution (33 months on average)
  • central distribution in between
19
Q

In PLEVA/PLC, _____ predominate within the infiltrate which helps distinguish from majority of other conditions in the differential.

A
  • CD8+ t-cells!!!