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1.
Eur Arch Otorhinolaryngol ; 280(4): 1647-1651, 2023 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-36074160

RESUMO

PURPOSE: The objective of the study was to evaluate the proposed cochlear duct length estimation based on the cochlear 'A value'. Furthermore, we assessed the interobserver variability between radiology and otolaryngology attending physicians and otolaryngology trainees. METHODS: Thirteen pediatric cochlear implant candidates were retrospectively analyzed by three otolaryngology physicians (attending physician, second year, and fourth year trainees) and a radiology attending. The cochlear duct length was calculated based on the formula of Grover et al. The differences in acquired measurements between observers were compared using the Wilcoxon matched signed-rank test. RESULTS: The differences in measurements between the attending otolaryngologist and radiologist were not statistically different, while several significant differences were observed with regard to measurements of attending doctors compared to both residents. In particular, a significant difference between the second year otolaryngology resident and otolaryngology and radiology attending was observed for one side (right ear p = 0.034 and p = 0.012, respectively). Moreover, the fourth year resident calculated significantly different cochlear duct measurements when compared to the attending otolaryngologist (left ear p = 0.014) and radiologist (right ear p = 0.047). Interestingly, differently experienced otolaryngology residents provided significantly different measurements for both ears. CONCLUSIONS: Based on these results, cochlear duct length measurement according to the proposed method may be a reliable and cost-effective method. Indeed, otolaryngology training may be sufficient to provide measurements comparable to radiologists. On the other hand, additional efforts should be invested during otolaryngology training in terms of the evaluation of radiological imaging which may increase the capabilities of otolaryngology residents in this regard.


Assuntos
Implante Coclear , Implantes Cocleares , Humanos , Criança , Variações Dependentes do Observador , Estudos Retrospectivos , Implante Coclear/métodos , Ducto Coclear
2.
Acta Neurol Belg ; 111(3): 241-4, 2011 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-22141293

RESUMO

Wegener's granulomatosis (WG) is a systemic vasculitis that can affect any organic system, but primarily involves the upper and lower respiratory tracts and the kidneys. WG relatively frequently affects the nervous system (in 30-50%), usually in the form of peripheral or cranial neuropathy. Involvement of the brain is reported in a very small percentage of patients (2%-8%). Three major mechanisms have been described as the cause of central nervous system (CNS) disease in WG: contiguous invasion of granuloma from extracranial sites, remote intracranial granuloma and CNS vasculitis. CNS involvement caused by contiguous invasion of granuloma from extracranial sites is the rarest. We report the case of a 37-year-old man with WG, manifested as a pulmonary and paranasal sinuses disease, with orbital and CNS involvement, caused by contiguous invasion from the paranasal sinuses. In this report, the rich spectrum of findings achieved by computed tomography and magnetic resonance are demonstrated. The importance of computed tomography in bony destruction PNS findings, and the importance of MR imaging in evaluation of the direct intracranial spread from nasal, paranasal and orbital disease are also emphasized.


Assuntos
Encefalopatias , Granulomatose com Poliangiite , Imageamento por Ressonância Magnética , Doenças Orbitárias , Doenças dos Seios Paranasais , Tomografia Computadorizada por Raios X , Adulto , Encefalopatias/diagnóstico por imagem , Encefalopatias/etiologia , Encefalopatias/patologia , Granulomatose com Poliangiite/complicações , Granulomatose com Poliangiite/diagnóstico por imagem , Granulomatose com Poliangiite/patologia , Humanos , Masculino , Doenças Orbitárias/diagnóstico por imagem , Doenças Orbitárias/etiologia , Doenças Orbitárias/patologia , Doenças dos Seios Paranasais/diagnóstico por imagem , Doenças dos Seios Paranasais/etiologia , Doenças dos Seios Paranasais/patologia
3.
Med Arh ; 65(6): 375-7, 2011.
Artigo em Inglês | MEDLINE | ID: mdl-22299305

RESUMO

PURPOSE: To present a case of Terson's syndrome consequent to ruptured intracranial aneurism treated successfully with a combined therapeutic approach. METHODS: Case report. A 37 year old man was urgently referred to the UCC Tuzla with sudden headache, vomiting and unconsciousness. CT scan showed ruptured aneurism of anterior communicant artery with signs of retinal thickening. Later ocular examination showed the massive bilateral vitreous haemorrhage. RESULTS: Patient was treated with medicamentous therapy for 7 months with no significant improvement. 7 months after aneurism rupture patient agreed to a surgical treatment. Right eye was treated surgically and left eye continued with conservative therapy. Visual acuity after vitrectomy improved in right eye to 1.0 and 0.5 in left eye. CONCLUSIONS: Terson's syndrome is relatively common complication of subarchnoid haemorrhage. Vitrectomy is safe and efficient approach to treat patients with Terson's syndrome.


Assuntos
Aneurisma Roto/complicações , Aneurisma Intracraniano/complicações , Hemorragia Vítrea/etiologia , Adulto , Aneurisma Roto/terapia , Terapia Combinada , Humanos , Aneurisma Intracraniano/terapia , Masculino , Síndrome , Hemorragia Vítrea/terapia
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