TY - JOUR
T1 - Immunologic Abnormalities Associated With Primary Anetoderma
AU - Hodak, Emmilia
AU - Shamai-Lubovitz, Orna
AU - David, Michael
AU - Hazaz, Bilha
AU - Katzenelson-Weissman, Varda
AU - Lahav, Meir
AU - Sandbank, Miriam
PY - 1992/6
Y1 - 1992/6
N2 - 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. (Arch Dermatol. 1992;128:799-803).
AB - 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. (Arch Dermatol. 1992;128:799-803).
UR - http://www.scopus.com/inward/record.url?scp=0026693235&partnerID=8YFLogxK
U2 - 10.1001/archderm.1992.01680160083009
DO - 10.1001/archderm.1992.01680160083009
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AN - SCOPUS:0026693235
SN - 0003-987X
VL - 128
SP - 799
EP - 803
JO - Archives of Dermatology
JF - Archives of Dermatology
IS - 6
ER -