4
views
0
recommends
+1 Recommend
0 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: not found

      Cutaneous manifestations of pediatric granulomatosis with polyangiitis: a clinicopathologic and immunopathologic analysis.

      Read this article at

      ScienceOpenPublisherPubMed
      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Granulomatosis with polyangiitis (GPA) is a rare systemic vasculitis associated with variable cutaneous manifestations and histopathologic findings. It is less frequent in children than adults and is often positive for cytoplasmic antineutrophil cytoplasmic antibody (ANCA) or proteinase 3-ANCA.

          Related collections

          Author and article information

          Journal
          J. Am. Acad. Dermatol.
          Journal of the American Academy of Dermatology
          1097-6787
          0190-9622
          May 2015
          : 72
          : 5
          Affiliations
          [1 ] Department of Dermatology, Mayo Clinic, Rochester, Minnesota.
          [2 ] Department of Dermatology, Mayo Clinic, Rochester, Minnesota; Division of Anatomic Pathology, Mayo Clinic, Rochester, Minnesota. Electronic address: gibson.lawrence@mayo.edu.
          Article
          S0190-9622(15)00110-3
          10.1016/j.jaad.2015.01.043
          25748311
          13bb4ab5-325e-4ac0-91a3-d52b2c1d2bcd
          Copyright © 2015 American Academy of Dermatology, Inc. Published by Elsevier Inc. All rights reserved.
          History

          Wegener granulomatosis,acneiform lesions,antineutrophil cytoplasmic antibodies,cytoplasmic antineutrophil cytoplasmic antibody,granuloma,granulomatosis with polyangiitis,granulomatous inflammation,palpable purpura,proteinase 3 antineutrophil cytoplasmic antibody,vasculitis

          Comments

          Comment on this article