Papulosquamous Diseases

General Information on Papulosquamous Diseases

  • the papulosquamous diseases are generally scaly, like the eczematous diseases
  • difference from the eczemas

1)     epidermis is generall thicker

2)     more clinically elevated scaly condition

3)     better described as a plaque than a patch

4)     eventually develop acanthosis and hyperkeratosis to a greater degree

5)     more sharply defined

  • some diseases may be both papulosquamous or eczematous depending on the stage

Specific Papulosquamous Diseases

Psoriasis

  • familial disease involving 1% of the population
  • may begin at any age; usually starts in adulthood
  • sharply-demarcated plaques with a ham-red color and thick, heaped-up silvery scales
  • lesions occur most commonly in areas of trauma – “Koebner phenomenon”
  • involves elbows, knees, scalp, buttocks, and intergluteal cleft
  • avoids areas like the face because the UV light helps retard the lesions
  • associated sith severe nail changes
  • 5% of patients develop psoriatic arthritis
  • Biopsy: hyperkeratosis, acanthosis, parakeratosis, neutrophils in stratum corneum
  • Treatment: topical tar, corticosteroids, UV light, topical anthralin (maybe methotrexate)

Lichen Planus

  • idiopathic disorder
  • less scaly than the other papulosquamous disorders
  • Plaques have the 3 P’s
  • purple
  • polygonal
  • very pruitic
  • flat-topped plaques/ sharply-angulated straight edges resemble polygons
  • covered with a fine, reticulated scale – Wickham’s striae
  • Koebner phenomenon also seen as in psoriasis
  • Mucus membrane involvement common
  • Biopsy: bandlike infiltrate of lymphocytes and histiocytes

Lichen Simplex Chronicus (LSC)

  • eczema that became elevated enough to be called papulosquamous
  • less sharply-demarcated than the other papulosquamous diseases
  • commonly occurs in rubbed areas – posterior neck, upper back, lower back, anterior legs, genitalia
  • diagnosis implies no specific cause – only a scaly process that is being chronically rubbed
  • try to determine the 1o cause – tinea, contact dermatitis, scabies, atopical dermatitis

Pityriasis Rosea

  • acute, common disorder thought to be of viral origin
  • occurs in young adults
  • spontaneously resolves in 6 weeks
  • plaques are oval to annular
  • involve the trunk, proximal extremities, and rarely the face
  • often – a single 2-6 mm lesion (herald patch) occurs prior to the onset of numerous others
  • rule out 2osyphilis
  • Treatment: symptomatic relief or pruitis with topical steroids or oral anti-histamines

Secondary (2o) Syphilis

  • on the maculopapular, eczematous, and the papulosquamous list
  • associated with: headache, fever, lymphadenopathy, and palmar/plantar lesions
  • do Serology (RPR or VDRL)

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