Immunologic abnormalities associated with primary anetoderma.

BACKGROUND AND DESIGN Primary anetoderma is a rare cutaneous elastolytic disorder, the etiopathogenesis of which has not yet been established. Six patients with primary anetoderma were studied in an attempt to assess the role of the immunologic system in the elastolytic process. The investigation included the medical history, physical examination, routine blood tests, specific tests for collagen diseases, prothrombin time, activated partial thromboplastin time, thyroxine, indirect immunofluorescence test, and skin biopsies for histopathologic study and direct immunofluorescence. RESULTS Two of the patients presented with autoimmune disorders: the first had Graves' disease, lupus anticoagulant, and autoimmune hemolysis, and the second had systemic scleroderma. There were positive direct immunofluorescence findings in most of the patients. Furthermore, all of them were found to have serologic immunologic abnormalities, of which the most common was a positive antinuclear factor. CONCLUSIONS These findings indicate that there is an immunologic involvement in primary anetoderma.

[1]  E. Hodak,et al.  Primary anetoderma associated with a wide spectrum of autoimmune abnormalities. , 1991, Journal of the American Academy of Dermatology.

[2]  R. Bergman,et al.  An immunofluorescence study of primary anetoderma , 1990, Clinical and experimental dermatology.

[3]  P. Agache,et al.  Dermatological autoimmune diseases and the multiple autoimmune syndromes. , 1989, Acta dermato-venereologica. Supplementum.

[4]  S. Muller,et al.  The cutaneous immunopathology of necrobiosis lipoidica diabeticorum. , 1988, Archives of dermatology.

[5]  M. Meurer,et al.  Systemic scleroderma. Clinical and pathophysiologic aspects. , 1988, Journal of the American Academy of Dermatology.

[6]  M. Aricò,et al.  [A case of Schweninger-Buzzi anetoderma. Histologic and immunologic study]. , 1986, Giornale italiano di dermatologia e venereologia : organo ufficiale, Societa italiana di dermatologia e sifilografia.

[7]  R. Winkelmann,et al.  Monoclonal antibody studies in the skin lesions of patients with anetoderma. , 1985, Archives of dermatology.

[8]  R. Winkelmann,et al.  Histopathologic findings in anetoderma. , 1984, Archives of dermatology.

[9]  B. Moore,et al.  Anetoderma. Clinical findings, associations, and long-term follow-up evaluations. , 1984, Archives of dermatology.

[10]  J F Fries,et al.  The 1982 revised criteria for the classification of systemic lupus erythematosus. , 1982, Arthritis and rheumatism.

[11]  S. Kossard,et al.  Inflammatory macular atrophy: immunofluorescent and ultrastructural findings. , 1979, Journal of the American Academy of Dermatology.

[12]  F. C. Mcduffie,et al.  Cutaneous vessel immune deposits in rheumatoid arthritis. , 1976, Arthritis and rheumatism.

[13]  Cipollaro Ac Macular atrophy (Schweninger-Buzzi type); chronic discoid lupus erythematosus. , 1952 .

[14]  R. Nomland,et al.  SECONDARY MACULAR ATROPHY: A STUDY OF TWELVE CASES OCCURRING IN CONNECTION WITH VARIOUS DISORDERS, WITH CONSIDERATION OF THE PATHOLOGIC RELATIONSHIPS , 1937 .

[15]  Weber Fp Macular Atrophy of the Skin showing the Early raised Erythematous Stage, and associated with ordinary Vitiligo , 1917 .