Wegener Granulomatosis (WG) is a rare disease that can manifest initially with recurrent facial palse in the absence of any other symptom and in this case diagnosis could be missed for a long time. WG should be considered in all cases of multipe cranial palsy with unknown origin. This is a case report interesting for many specialist physicians ( ENT, ophthalmologists, rheumatologists, pneumologists)
"Hide and seek" with antineutrophil cytoplasmic antibodies / ALICANDRI CIUFELLI, Matteo; Molteni, Gabriele; Mascia, Maria Teresa; Genovese, Elisabetta; Presutti, Livio. - In: AMERICAN JOURNAL OF OTOLARYNGOLOGY. - ISSN 0196-0709. - ELETTRONICO. - 31:5(2010), pp. 397-398. [10.1016/j.amjoto.2009.05.005]
"Hide and seek" with antineutrophil cytoplasmic antibodies
ALICANDRI CIUFELLI, Matteo;MOLTENI, Gabriele;MASCIA, Maria Teresa;GENOVESE, Elisabetta;PRESUTTI, Livio
2010
Abstract
Wegener Granulomatosis (WG) is a rare disease that can manifest initially with recurrent facial palse in the absence of any other symptom and in this case diagnosis could be missed for a long time. WG should be considered in all cases of multipe cranial palsy with unknown origin. This is a case report interesting for many specialist physicians ( ENT, ophthalmologists, rheumatologists, pneumologists)
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