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Anetoderma before development of antiphospholipid antibodies: delayed development and monitoring of antiphospholipid antibodies in an SLE patient presenting with anetoderma.
Xia, Fan Di; Hoang, Mai P; Smith, Gideon P.
Afiliación
  • Xia FD; Harvard Medical School, Boston, MA, USA. fandi_xia@ hms.harvard.edu.
Dermatol Online J ; 23(3)2017 Mar 15.
Article en En | MEDLINE | ID: mdl-28329518
ABSTRACT

INTRODUCTION:

Anetoderma is an elastolytic skindisorder that has been associated with the presenceof antiphospholipid antibodies (aPL). Patients withantiphospholipid antibody-positive anetoderma havebeen reported to develop symptoms of Graves disease,antiphospholipid syndrome, and other autoimmuneconditions. The temporal relationship, however,between anetoderma onset and the emergence ofaPL remains unclear, a clarification of which may haveimplications for the screening and monitoring ofpatients with anetoderma. CASE Herein we report acase of a patient with systemic lupus erythematosuspresenting with anetoderma that preceded thedevelopment of aPL. The patient was found to havesubsequently developed IgM cardiolipin antibodiesat a serology follow-up approximately two years later.Conclusion and Relevance This finding suggests thatanetoderma can precede aPL seroconversion andthat patients with anetoderma may require continuedserology monitoring. Such long-term monitoring willbe important for identifying laboratory indicationsthat may portend the development of furtherautoimmune symptoms associated with anetoderma.
Asunto(s)
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Banco de datos: MEDLINE Asunto principal: Inmunoglobulina M / Anticuerpos Anticardiolipina / Anetodermia / Lupus Eritematoso Sistémico Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Año: 2017 Tipo del documento: Article
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Banco de datos: MEDLINE Asunto principal: Inmunoglobulina M / Anticuerpos Anticardiolipina / Anetodermia / Lupus Eritematoso Sistémico Tipo de estudio: Diagnostic_studies / Prognostic_studies Límite: Adult / Female / Humans Idioma: En Año: 2017 Tipo del documento: Article