2016
DOI: 10.1159/000442040
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Otologic and Rhinologic Manifestations of Eosinophilic Granulomatosis with Polyangiitis

Abstract: Background: Eosinophilic granulomatosis with polyangiitis (EGPA) is a systemic autoimmune disease that manifests as asthma, recurrent sinusitis and peripheral eosinophilia. In this study, we investigated the clinical features of the ear and nasal manifestations of EGPA in comparison with those of granulomatosis with polyangiitis (GPA). Materials and Methods: Twenty-one patients diagnosed with EGPA were studied. The frequency of otologic manifestations, the degree of hearing loss and the frequency of nasal symp… Show more

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Cited by 38 publications
(21 citation statements)
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“…ANCA positive 31%-58% 26,37 MPO ANCA positive 25%-50% 26,47 ENT involvement 48%-96% 37,38 Rhinologic CRSwNP 42%-51% 37,38 Change in sense of smell 40% 47 Nasal crusting 8%-43% 47,48 Otologic OME/CHL 3%-12% 26 59 although the importance of abstinence from cocaine for a good outcome cannot be overstated.…”
Section: Prevalence Of Ent Features Of Eosinophilic Granulomatosis Wimentioning
confidence: 99%
“…ANCA positive 31%-58% 26,37 MPO ANCA positive 25%-50% 26,47 ENT involvement 48%-96% 37,38 Rhinologic CRSwNP 42%-51% 37,38 Change in sense of smell 40% 47 Nasal crusting 8%-43% 47,48 Otologic OME/CHL 3%-12% 26 59 although the importance of abstinence from cocaine for a good outcome cannot be overstated.…”
Section: Prevalence Of Ent Features Of Eosinophilic Granulomatosis Wimentioning
confidence: 99%
“…We have included a group of lesions, framed as “other lesions”: 1) opacification, fibrosis and mucosal thickening, which is the most frequent radiological finding of the maxillary sinus [ 41 ], but which in our case was diagnosed as a polyp in the CRS; 2) a hyperostosis, which was confused with a benign tumour and which tend to be normal anatomical variations [ 43 ]; 3) an organized hematoma that was suspected to be malignant in a patient with chronic myeloid leukemia and that has been recently described [ 44 ]; 4) non-necrotizing granulomatous disease in a 33-year-old woman as part of a clinical picture of eosinophilic granulomatosis with polyangitis, an autoimmune systemic disease manifesting as asthma, recurrent sinusitis and peripheral eosinophilia [ 45 ].…”
Section: Discussionmentioning
confidence: 99%
“…Furthermore, specific forms of CRS have been described in sarcoidosis, Wegener’s granulomatosis, congenital or acquired disorders of mucociliary clearance and/or ciliary activity, as well as Churg–Strauss syndrome [ 1 , 100 , 104 ].…”
Section: Comorbidities Of Crsmentioning
confidence: 99%