Wegener granulomatosis (WG) is characterized by a classic triad of granulomatous inflammation of the respiratory tract, necrotizing vasculitis and nephritis. The absence of renal disease defines a subset of "limited WG". Approximately 50% of WG patients develop ophthalmic disease. The histopatological study and +c-ANCA were essential to make a definite diagnosis in these cases.
CITATION STYLE
Pereira, I. C., Zacharias, L. C., Zagui, R., Santo, R., & Matayoshi, S. (2007). Granulomatose de Wegener: relatos de casos. Arquivos Brasileiros de Oftalmologia, 70(6), 1010–1015. https://doi.org/10.1590/s0004-27492007000600024
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