Autor: |
Nicole R. Bender, Elizabeth L. Bisbee, Douglas Robins, Kiran Motaparthi, Vladimir Vincek |
Jazyk: |
angličtina |
Rok vydání: |
2022 |
Předmět: |
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Zdroj: |
Case Reports in Dermatology, Vol 14, Iss 1, Pp 12-18 (2022) |
Druh dokumentu: |
article |
ISSN: |
1662-6567 |
DOI: |
10.1159/000519658 |
Popis: |
Macular lymphocytic arteritis (MLA) is an indolent cutaneous small-medium-vessel vasculitis characterized by widespread asymptomatic livedo racemosa. A number of serologic abnormalities have been reported including an elevated erythrocyte sedimentation rate and antibodies associated with antiphospholipid antibody syndrome. We present a case of MLA with multiple serologic abnormalities, including those that have yet to be reported, such as anti-U1 ribonucleotide protein, anti-RNA polymerase III, anti-smith, and anti-proteinase 3 antibodies. We also provide a brief review of this unfamiliar entity with a focus on the appropriate workup. |
Databáze: |
Directory of Open Access Journals |
Externí odkaz: |
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