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anetoderma; dermatitis atrophicans maculosa

Classification: - inflammatory (Jadassohn-Pellizzari) - noninflammatory (Schweninger-Buzzi) Etiology: - primary (idiopathic) - secondary: - preceded by an inflammatory or other skin pathology in the same location - may be associated with systemic disease - a familial form has been described Pathology: - benign condition - focal loss of dermal elastic tissue - inflammatory & noninflammatory lesions are histologically similar Clinical manifestations: - localized areas of flaccid or herniated saclike skin - both inflammatory & noninflammatory lesions may be found in the same individual Laboratory: - thyroid autoantibodies - anti-thyroid peroxidase Ab - anti-thyroglobulin Ab - anti-thyrotropin receptor Ab - antiphospholipid antibody - lupus anticoagulant - anticardiolipin Ab - anti beta-2-glycoprotein 1 Ab - as indicated - complement C3 in serum, complement C4 in serum - serology - antinuclear antibody - anti-Ro antibody - anti-La antibody - antimitochonrial antibody - anti-smooth muscle antibody - serum ACE activity - complete blood count - erythrocyte sedimentation rate - Lyme disease serology (titer) - PPD - RPR Management: - no effective treatment - surgical excision may be an option if lesions are small & few

General

skin disease (dermatologic disorder, dermatopathy, dermatosis)

References

  1. Wikipedia: Anetoderma http://en.wikipedia.org/wiki/Anetoderma
  2. Laumann AE and Elston DM Medscape: eMedicine: Anetoderma http://emedicine.medscape.com/article/1073850-overview