An Atypical Case of Granulomatosis with Polyangiitis with Cutaneous Features in a 19-year-old Female

Main Article Content

Daniel Fischer
St. John's Episcopal Hospital

Rebeca Teplitz
St. John's Episcopal Hospital

Graham Litchman
St. John's Episcopal Hospital

Suzanne Sirota Rozenberg
St. John's Episcopal Hospital

Keywords

granulomatosis with polyangitis, Wegener's, vasculitis, atypical, cutaneous, hyperthyroid, punched, out, ulcers

References

1. E. Ntatsaki, R. A. Watts, and D. G. I. Scott, “Epidemiology of ANCA-associated vasculitis,” Rheum. Dis. Clin. North Am., vol. 36, no. 3, pp. 447–461, Aug. 2010.

2. L. E. Gibson, U. Specks, and H. Homburger, “Clinical utility of ANCA tests for the dermatologist,” Int. J. Dermatol., vol. 42, no. 11, Nov. 2003, doi: 10.1046/j.1365-4362.2003.01914.x.

3. G. Ragab, M. T. Hegazy, M. Ali, M. R. E. Abdel-Halim, and X. Puéchal, “Three Patterns of Cutaneous Involvement in Granulomatosis with Polyangiitis,” Journal of Advanced Research, vol. 24, p. 311, Jul. 2020.

4. R. Micheletti, Z. Chiesa, A. Craven, R. Watts, R. Luqmani, and P. Merkel, “LB943 Cutaneous manifestations of ANCA-associated vasculitis are common, varied, and associated with systemic disease,” Journal of Investigative Dermatology, vol. 137, no. 10. p. B3, 2017. doi: 10.1016/j.jid.2017.07.016.

5. S. Lionaki et al., “Association between thyroid disease and its treatment with ANCA small-vessel vasculitis: a case–control study,” Nephrol. Dial. Transplant, vol. 22, no. 12, pp. 3508–3515, Aug. 2007.

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Published
Nov 16, 2022
DOI https://doi.org/10.25251/skin.6.6.15

Article Details

How to Cite
Fischer, D. ., Teplitz, R., Litchman, G., & Rozenberg, S. S. (2022). An Atypical Case of Granulomatosis with Polyangiitis with Cutaneous Features in a 19-year-old Female. SKIN The Journal of Cutaneous Medicine, 6(6), 539–541. https://doi.org/10.25251/skin.6.6.15
Issue
Vol. 6 No. 6 (2022): November Issue & Poster Presentations from FC22 Dermatology Conference®
Section
Brief Articles
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