https://orcid.org/0000-0002-7344-8039
References
- Tintle SJ, Cruse AR, Brodell RT, Duong B. Classic findings, mimickers, and distinguishing features in primary blistering skin disease. Arch Pathol Lab Med. 2020;144(2):136–147. doi:10.5858/arpa.2019-0175-RA
- Bickle KM, Roark TK, Hsu S. Autoimmune bullous dermatoses: a review. Am Fam Physician. 2002;65(9):1861.
- Taghipour K, Perera GK. Autoimmune blistering skin diseases. Medicine. 2013;41(7):387–393. doi:10.1016/j.mpmed.2013.04.021
- Greco A, Marinelli C, Fusconi M, et al. Clinic manifestations in granulomatosis with polyangiitis. Int J Immunopathol Pharmacol. 2016;29(2):151–159. doi:10.1177/0394632015617063
- Lutalo PM, D’Cruz DP. Diagnosis and classification of granulomatosis with polyangiitis (aka Wegener’s granulomatosis). J Autoimmun. 2014;48:94–98. doi:10.1016/j.jaut.2014.01.028
- Marzano AV, Raimondo MG, Berti E, Meroni PL, Ingegnoli F. Cutaneous manifestations of ANCA-associated small vessels vasculitis. Clin Rev Allergy Immunol. 2017;53(3):428–438.
- Pagnoux C, Guillevin L. Treatment of granulomatosis with polyangiitis (Wegener’s). Expert Rev Clin Immunol. 2015;11(3):339–348. doi:10.1586/1744666X.2015.1008455
- Flossmann O, Berden A, de Groot K, et al. Long-term patient survival in ANCA-associated vasculitis. Ann Rheum Dis. 2011;70(3):488–494. doi:10.1136/ard.2010.137778
- Rottem M, Fauci AS, Hallahan CW, et al. Wegener granulomatosis in children and adolescents: clinical presentation and outcome. J Pediatr. 1993;122(1):26–31. doi:10.1016/S0022-3476(05)83482-1
- Scott DG, Watts RA. Systemic vasculitis: epidemiology, classification and environmental factors. Ann Rheum Dis. 2000;59(3):161–163. doi:10.1136/ard.59.3.161
- Martínez-Morillo M, Grados D, Naranjo-Hans D, Mateo L, Holgado S, Olivé A. Granulomatosis con poliangeítis (Wegener). Descripción de 15 casos. Reumatol Clin. 2012;8(1):15–19. doi:10.1016/j.reuma.2011.04.009
- Francès C, Piette J-C, Saada V, et al. Wegener’s granulomatosis: dermatological manifestations in 75 cases with clinicopathologic correlation. Arch Dermatol. 1994;130(7):861–867. doi:10.1001/archderm.1994.01690070055008
- Weedon D. Vasculitis with Granulomatosis. Weedon’s Skin Pathology. 4th ed. London: Churchil Livingstone Elsevier; 2015:271–276.
- Jayne D. Conventional treatment and outcome of Wegener’s granulomatosis and microscopic polyangiitis. Cleve Clin J Med. 2002;69(2):SII110–SII115. doi:10.3949/ccjm.69.Suppl_2.SII110
- Tarzi RM, Pusey CD. Current and future prospects in the management of granulomatosis with polyangiitis (Wegener’s granulomatosis). Ther Clin Risk Manag. 2014;10:279. doi:10.2147/TCRM.S41598
- Mekkes J, Loots M, Van Der Wal A, Bos J. Causes, investigation and treatment of leg ulceration. Br J Dermatol. 2003;148(3):388–401. doi:10.1046/j.1365-2133.2003.05222.x