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Early diagnosis of Wegener's granulomatosis presenting with facial nerve palsy

Published online by Cambridge University Press:  29 June 2007

J. D. Hern ,
L. J. Hollis ,
G. Mochloulis ,
P. Q. Montgomery  and
N. S. Tolley
J. D. Hern
Affiliation:
Department of Otolaryngology, St Mary's Hospital, Paddington, London, UK.
L. J. Hollis
Affiliation:
Department of Otolaryngology, St Mary's Hospital, Paddington, London, UK.
G. Mochloulis
Affiliation:
Department of Otolaryngology, St Mary's Hospital, Paddington, London, UK.
P. Q. Montgomery*
Affiliation:
Department of Otolaryngology, St Mary's Hospital, Paddington, London, UK.
N. S. Tolley
Affiliation:
Department of Otolaryngology, St Mary's Hospital, Paddington, London, UK.
*
Address for correspondence: P. Q. Montgomery, F.R.C.S., Department of Otolaryngology, St Mary's Hospital, Paddington, London W2 1NY. Fax: 0171 725 1847
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Abstract

Wegener's granulomatosis is a multi-system disease characterized by granuloma formation and a necrotizing vasculitis. It classically presents with involvement of the upper and lower respiratory and renal systems. However locoregional disease is common and may include otological manifestations. Facial nerve palsy has been reported during the course of the disease process but it is extremely rare for it to be the presenting feature. Previously reported cases have involved a protracted diagnostic process including exploratory tympanotomy, mastoidectomy and facial nerve decompression. We report a case of Wegener's granulomatosis which presented with a facial nerve palsy. An early diagnosis was achieved by measurement of the erythrocyte sedimentation rate (ESR), followed by serological assay of cytoplasmic anti-neutrophil cytoplasmic antibody (cANCA). Histological examination of nasal mucosal biopsies confirmed granuloma formation consistent with a diagnosis of Wegener's granulomatosis. This allowed early treatment with immunosuppressive therapy and avoided unnecessary and potentially hazardous middle ear surgery.

Keywords

Wegener's granulomatosisFacial paralysis
Type
Clinical Records
Information
The Journal of Laryngology & Otology , Volume 110 , Issue 5 , May 1996 , pp. 459 - 461
Copyright
Copyright © JLO (1984) Limited 1996

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References

Bradley, P. J. (1983) Wegener's granulomatosis of the ear. Journal of Laryngology and Otology 97: 623–626.CrossRefGoogle ScholarPubMed
Calonius, I. H., Christensen, C. K. (1980) Hearing impairment and facial palsy as the initial signs of Wegener's granulomatosis. Journal of Laryngology and Otology 94: 649–657.CrossRefGoogle ScholarPubMed
Fanci, A. S., Wolff, S. M. (1973) Wegener's granulomatosis: studies in eighteen patients with a review of the literature. Medicine (Baltimore) 52: 535–561.Google Scholar
Fenton, J. E., O'Sullivan, T. J. (1994) The otological manifestations of Wegener's granulomatosis. Journal of Laryngology and Otology 108: 144–146.CrossRefGoogle ScholarPubMed
Gross, W. L., Schmitt, W. H., Csernok, E. (1991) Antibeutrophil cytoplasmic autoantibody-associated diseases: a rheumatologist's perspective. American Journal of Kidney Disease 18: 175–179.CrossRefGoogle Scholar
Hugh Powers, W. (1974) Peripheral facial paralysis and systemic disease. Otolaryngologic Clinics of North America 7: 397–404.CrossRefGoogle Scholar
Macias, J. D., Wackym, P. A., McCabe, B. F. (1993) Early diagnosis of otological Wegener's granulomatosis using the serological marker c-ANCA. Annals of Otology, Rhinology and Laryngology 102: 337–341.CrossRefGoogle ScholarPubMed