scholarly journals A Case of Wegener’s Granulomatosis Presenting with Unilateral Facial Nerve Palsy

2016 ◽  
Vol 2016 ◽  
pp. 1-3 ◽  
Author(s):  
Roy Ujjawal ◽  
Pan Koushik ◽  
Panwar Ajay ◽  
Chakrabarti Subrata
Keyword(s):  
Facial Nerve ◽  
Wegener’S Granulomatosis ◽  
Nerve Palsy ◽  
Acute Inflammation ◽  
Granulomatosis With Polyangiitis ◽  
Medical Literature ◽  
Facial Nerve Palsy ◽  
Renal Involvement ◽  
Wegener's Granulomatosis ◽  
Classical Triad

Wegener’s granulomatosis or granulomatosis with polyangiitis is a necrotizing vasculitis affecting both arterioles and venules. The disease is characterized by the classical triad involving acute inflammation of the upper and lower respiratory tracts with renal involvement. However, the disease pathology can affect any organ system. This case presents Wegener’s granulomatosis presenting with facial nerve palsy as the first manifestation of the disease, which is rarely reported in medical literature.

scholarly journals Granulomatosis with polyangiitis presenting with unilateral facial nerve palsy and nasal septum perforation

2021 ◽  
Vol 14 (1) ◽  
pp. e236469
Author(s):  
Bandar Zaeri ◽  
Soha Khan ◽  
Asmaa Hegazy ◽  
Nayef Al Ghanim
Keyword(s):  
Facial Nerve ◽  
Nerve Palsy ◽  
Granulomatosis With Polyangiitis ◽  
Facial Nerve Palsy ◽  
Renal Involvement ◽  
Septum Perforation ◽  
The Central Nervous System ◽  
Systemic Manifestations ◽  
Classical Triad ◽  
Nasal Septum Perforation

Granulomatosis with polyangiitis (GPA) is a necrotising vasculitis of unknown cause that has several systemic manifestations. The disease is characterised by the classical triad involving acute inflammation of the upper and lower respiratory tracts with renal involvement. However, the disease pathology can involve the central nervous system. This case report presents a case of GPA with facial nerve palsy as the first manifestation of the disease, which has been rarely reported in the medical literature.

Fatal course of Wegener's granulomatosis with bilateral otomastoiditis and bilateral facial nerve palsy

2008 ◽  
Vol 138 (6) ◽  
pp. 799-800 ◽  
Author(s):  
F. Preuss Simon ◽  
Markus Stenner ◽  
Dirk Beutner ◽  
Matthias Laudes ◽  
Jens Peter Klussmann
Keyword(s):  
Facial Nerve ◽  
Wegener’S Granulomatosis ◽  
Nerve Palsy ◽  
Facial Nerve Palsy ◽  
Wegener's Granulomatosis ◽  
Fatal Course

Hearing impairment and facial palsy as initial signs of Wegener's granulomatosis

1980 ◽  
Vol 94 (6) ◽  
pp. 649-657 ◽  
Author(s):  
I. H. Calonius ◽  
C. K. Christensen
Keyword(s):  
Facial Nerve ◽  
Hearing Impairment ◽  
Otitis Media ◽  
Wegener’S Granulomatosis ◽  
Nerve Palsy ◽  
Facial Nerve Palsy ◽  
Wegener's Granulomatosis ◽  
The Other ◽  
Treatment Resistant ◽  
Serous Otitis Media

SummaryIn two patients with Wegener's granulomatosis, treatment-resistant serous otitis media was followed by unilateral facial nerve palsy. Later both patients developed uraemia due to extracapillary glomerulonephritis. In one of them, who was treated with prednisone and cyclophosphamide, renal function improved, while in the other patient it remained impaired. Both patients suffered lasting hearing impairment in spite of general improvement during the course of the disease. The facial nerve palsy improved slightly in one, while no improvement was seen in the other.The possibility of Wegener's granulomatosis or other autoimmune collagen diseases should be considered in cases of treatment-resistant serous otitis media. Early diagnosis and treatment can possibly save the patient from the lifethreatening consequences of these diseases.

Wegener's granulomatosis presenting with bilateral facial nerve palsy

2001 ◽  
Vol 258 (4) ◽  
pp. 198-202 ◽  
Author(s):  
A. C. Nikolaou ◽  
Konstantinos C. Vlachtsis ◽  
Michalis A. Daniilidis ◽  
Dimitrios G. Petridis ◽  
Ioannis C. Daniilidis
Keyword(s):  
Facial Nerve ◽  
Wegener’S Granulomatosis ◽  
Nerve Palsy ◽  
Facial Nerve Palsy ◽  
Wegener's Granulomatosis

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

1996 ◽  
Vol 110 (5) ◽  
pp. 459-461 ◽  
Author(s):  
J. D. Hern ◽  
L. J. Hollis ◽  
G. Mochloulis ◽  
P. Q. Montgomery ◽  
N. S. Tolley
Keyword(s):  
Early Diagnosis ◽  
Facial Nerve ◽  
Wegener’S Granulomatosis ◽  
Nerve Palsy ◽  
Facial Nerve Palsy ◽  
Disease Process ◽  
Wegener's Granulomatosis ◽  
Granuloma Formation ◽  
Diagnostic Process ◽  
Middle Ear Surgery

AbstractWegener'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.

Otologic Wegener's Granulomatosis with Facial Nerve Palsy

1998 ◽  
Vol 107 (7) ◽  
pp. 555-559 ◽  
Author(s):  
Paul Dagum ◽  
Joseph B. Roberson
Keyword(s):  
Facial Nerve ◽  
Wegener’S Granulomatosis ◽  
Nerve Palsy ◽  
Facial Nerve Palsy ◽  
Correct Diagnosis ◽  
Cranial Nerves ◽  
Serum Levels ◽  
Antineutrophil Cytoplasmic Antibody ◽  
Wegener's Granulomatosis ◽  
Facial Nerve Decompression

Wegener's granulomatosis, characterized by necrotizing granulomas and vasculitis of the respiratory tract and kidney, frequently first presents with otologic symptoms. We report a case of primary otologic Wegener's granulomatosis in a patient who presented with symptoms of acute otomastoiditis and associated facial nerve palsy. The patient subsequently developed neuropathies of various cranial nerves. The patient underwent urgent mastoidectomy with facial nerve decompression. Nonspecific inflammatory disease of the mastoid mucosa delayed the correct diagnosis of Wegener's granulomatosis, which was confirmed by an elevated level of cytoplasmic-pattern antineutrophil cytoplasmic antibody (cANCA). We contrast the specificity of middle ear mucosal disease and cANCA serum levels in the diagnosis of Wegener's granulomatosis.

Early diagnosis and stage-adapted treatment of Wegener’s granulomatosis

2003 ◽  
Vol 117 (3) ◽  
pp. 208-211 ◽  
Author(s):  
G. Cadoni ◽  
S. Agostino ◽  
E. Campobasso ◽  
P. Vulpiani ◽  
R. Manna ◽  
...  
Keyword(s):  
Facial Nerve ◽  
Wegener’S Granulomatosis ◽  
Facial Nerve Palsy ◽  
Clinical Symptoms ◽  
Chronic Otitis Media ◽  
Wegener's Granulomatosis ◽  
Definitive Diagnosis ◽  
Early Assessment ◽  
Disease Remission ◽  
Facial Nerve Decompression

A case of Wegener’s granulomatosis (WG) presenting with hearing loss and right facial nerve palsy is reported. The definitive diagnosis was based upon clinical data and serum cANCA and AECA detection. Early assessment of WG prevented surgical facial nerve decompression to treat a chronic otitis media complication. Immunosuppressive therapy with steroids, cyclophosphamide and methotrexate was required for relief of clinical symptoms and cANCA negativity as an expression of disease remission. The effectiveness of co-trimoxazole for preventing relapses of WG is discussed.

Granulomatosis with polyangiitis presenting as facial nerve palsy in a teenager

2018 ◽  
Vol 107 ◽  
pp. 160-163
Author(s):  
James C. Wang ◽  
Brittany A. Leader ◽  
Ryan A. Crane ◽  
Bernadette L. Koch ◽  
Matthew M. Smith ◽  
...  
Keyword(s):  
Facial Nerve ◽  
Nerve Palsy ◽  
Granulomatosis With Polyangiitis ◽  
Facial Nerve Palsy

scholarly journals Bilateral Ureteral Stenosis with Hydronephrosis as First Manifestation of Granulomatosis with Polyangiitis (Wegener’s Granulomatosis): A Case Report and Review of the Literature

2020 ◽  
Vol 2020 ◽  
pp. 1-6
Author(s):  
Joelle Suillot ◽  
Jürg Bollmann ◽  
Samuel Rotman ◽  
Eric Descombes
Keyword(s):  
Wegener’S Granulomatosis ◽  
Crescentic Glomerulonephritis ◽  
Granulomatosis With Polyangiitis ◽  
Renal Involvement ◽  
Wegener's Granulomatosis ◽  
High Dose ◽  
Review Of The Literature ◽  
Ureteral Stenosis ◽  
Rare Manifestation ◽  
Unilateral Hydronephrosis

Ureteral stenosis is a rare manifestation of granulomatosis with polyangiitis (formerly known as Wegener’s granulomatosis). We report the case of a 76-year-old woman with progressive renal failure in which bilateral hydronephrosis due to ureteral stenosis was the first manifestation of the disease. Our patient also had renal involvement with pauci-immune crescentic glomerulonephritis associated with high titers of anti-proteinase 3 c-ANCAs, but no involvement of the upper or lower respiratory tract. The hydronephrosis and renal function rapidly improved under immunosuppressive therapy with high-dose corticosteroids and intravenous pulse cyclophosphamide. We reviewed the literature and found only ten other reported cases of granulomatosis with polyangiitis/Wegener’s granulomatosis and intrinsic ureteral stenosis: in two cases, the presenting clinical manifestation was unilateral hydronephrosis and in only two others was the hydronephrosis bilateral, but this complication developed during a relapse of the disease. This case emphasizes the importance of including ANCA-related vasculitis in the differential diagnosis of unusual cases of unilateral or bilateral ureteral stenosis.

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