Serologic Abnormalities in Macular Lymphocytic Arteritis with Case Presentation
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.
- Standort
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Deutsche Nationalbibliothek Frankfurt am Main
- Umfang
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Online-Ressource
- Sprache
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Englisch
- Erschienen in
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Serologic Abnormalities in Macular Lymphocytic Arteritis with Case Presentation ; volume:14 ; number:1 ; year:2022 ; pages:12-18 ; extent:7
Case reports in dermatology ; 14, Heft 1 (2022), 12-18 (gesamt 7)
- Urheber
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Bender, Nicole R.
Bisbee, Elizabeth L.
Robins, Douglas
Motaparthi, Kiran
Vincek, Vladimir
- DOI
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10.1159/000519658
- URN
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urn:nbn:de:101:1-2022051200185725097207
- Rechteinformation
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Open Access; Der Zugriff auf das Objekt ist unbeschränkt möglich.
- Letzte Aktualisierung
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15.08.2025, 07:28 MESZ
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Beteiligte
- Bender, Nicole R.
- Bisbee, Elizabeth L.
- Robins, Douglas
- Motaparthi, Kiran
- Vincek, Vladimir
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