The diagnostic accuracy of MRI in determining the relations between paraclinoid aneurysms and the cavernous sinus.

PURPOSE: The location of paraclinoid aneurysms is determinant for evaluation of its intradural compartment and risk of SAH after rupture. Advanced MRI techniques have provided clear visualization of the distal dural ring (DDR) to determine whether an aneurysm is intracavernous, transitional or intradural for decision-making. We analyzed the diagnostic accuracy of MRI in predicting whether a paraclinoid aneurysm is intracavernous, transitional or intradural. METHODS: We conducted a prospective cohort between January 2014 and December 2018. Patients with paraclinoid aneurysms underwent 3D fast spin-echo MRI sequence before surgical treatment. The DDR was the landmark for MRI characterization of the aneurysms as follow: (i) Intradural; (ii) Transitional; and (iii) Intracavernous. The MRI sensitivity, specificity, positive and negative likelihood ratios were determined compared to the intraoperative findings. We also evaluated the intertechnique agreement using the Cohen's kappa coefficient (κ) for dichotomous classifications (cavernous vs non-cavernous). RESULTS: Twenty patients were included in the cohort. The accuracy of MRI showed a sensitivity of 86.7% (95%CI:59.5-98.3) and specificity of 90.0% (95%CI:55.5-99.8). Analyzing only patients without history of SAH, accuracy test improved with a sensitivity of 92.3% (95%CI:63.9-99.8) and specificity reached 100% (95%CI: 63-100). Values of Cohen's kappa (κ), intertechnique agreement was considered substantial for dichotomous classifications (κ = 0.754; p < 0.001). For patients without previous SAH, intertechnique agreement was even more coincident for the dichotomous classification (κ = 0.901; p < 0.001). CONCLUSION: 3D fast spin-echo MRI sequence is a reliable and useful technique for determining the location of paraclinoid aneurysms in relation to the cavernous sinus, particularly for patients with no history of SAH.

Calvarial ectopic meningothelial meningioma.

BACKGROUND: Meningiomas are the most common benign neoplasm of the brain whereas ectopic presentation, although reported, is rare. Among these ectopic tumors, there are a group of purely intraosseous meningiomas, which usually are diagnosed differentially from common primary osseous tumor such as fibrous dysplasia and osteoid osteoma. CASE DESCRIPTION: We report a 62-year-old female with a history of headaches and 6 months of progressive right parietal bulging, with no neurological signs. Parietal craniotomy was performed with immediate titanium cranioplasty of the parietal convexity. Histopathology exams revealed an ectopic intradiploic meningioma without invasion of cortical layers, with positive staining for progesterone receptors and epithelial membrane antigen. CONCLUSIONS: Ectopic intraosseous meningiomas remain a rare neoplasm with only a few cases reported. The main theories to justify the unusual topography appear to be embryological remains of neuroectodermal tissue or cellular dedifferentiation. Surgical treatment seems the best curative option.

Audiologic evaluation in patients with acquired hypothyroidism.

UNLABELLED: Hearing loss in hypothyroidism has been reported by many authors but its pathophysiology is unclear. AIMS: to study the audiological evaluation of patients with acquired hypothyroidism. MATERIALS AND METHODS: two groups were included: a hypothyroidism group (HG, n-30), and a control group (CG, n-30). Parameters studied: gender, time of hypothyroidism, comorbidities, cochleovestibular symptoms, biochemistry and hormonal exams (TSH, T4), tonal audiometry, TOAEs and BERA. RESULTS: all participants were women, 70% of the HG had Hashimoto thyroiditis, 60% of the HG had had the diagnostic of the hypothyroidism for at least five years. Depression and hypertension were frequent in HG. All HG patients had altered TSH values and 50% had diminished T4 values. Sensorineural hearing loss was detected in 22 ears from the HG and in seven from the CG. BERA was normal in the CG and altered in 10 ears from the HG, showing L-V increase. TOAEs were absent in 12 ears from the HG and in four from the CG. CONCLUSIONS: HG patients had more cochleovestibular symptoms, higher audiometric thresholds, increase in L-V in the BERA and absence or reduction in TOAEs amplitudes. Such alterations were not associated with THS and free T4 levels.

Avaliação audiológica em pacientes portadores de hipotireoidismo / Audiologic evaluation in patients with acquired hypothyroidism

Surdez no hipotireoidismo já foi descrita por diversos autores, porém a fisiopatologia é incerta. OBJETIVOS: Realizar avaliações audiológicas de pacientes com hipotireoidismo adquirido. MATERIAL E MÉTODOS: Grupos de estudo: hipotireoidismo (GH, n-30) e controle (GC, n-30). Parâmetros estudados: gênero, tempo do hipotireoidismo, co-morbidades, sintomas cócleo-vestibulares, exames bioquímicos e hormonais, limiares audiométricos, PEATE e EOAT. RESULTADOS: Todos os participantes eram mulheres; em GH 70 por cento dos pacientes apresentavam tireoidite de Hashimoto e 60 por cento tinham diagnóstico de hipotireoidismo há mais de 5 anos. Depressão e hipertensão foram as principais co-morbidades do grupo GH. Todos os pacientes de GH tinham valores elevados de TSH e 50 por cento deles apresentavam diminuição de T4 livre. Surdez neurossensorial foi detectada em 22 orelhas de GH e em 7 de GC. PEATE mostrou-se normal nos participantes do GC e alterado em 10 orelhas do GH, havendo predomínio do aumento de L-V. EOAT estiveram ausentes em 12 orelhas de GH e em 4 de GC. CONCLUSÕES: Os pacientes com hipotireoidismo apresentaram mais sintomas cócleo-vestibulares, limiares audiométricos mais elevados, prolongamento das latências absolutas de L-V no PEATE e ausência ou redução as amplitudes das emissões otoacústicas. Tais alterações não estavam associadas aos níveis de TSH e T4 livre.

Hearing loss in hypothyroidism has been reported by many authors but its pathophysiology is unclear. AIMS: to study the audiological evaluation of patients with acquired hypothyroidism. MATERIALS AND METHODS: two groups were included: a hypothyroidism group (HG, n-30), and a control group (CG, n-30). Parameters studied: gender, time of hypothyroidism, comorbidities, cochleovestibular symptoms, biochemistry and hormonal exams (TSH, T4), tonal audiometry, TOAEs and BERA. RESULTS: all participants were women, 70 percent of the HG had Hashimoto thyroiditis, 60 percent of the HG had had the diagnostic of the hypothyroidism for at least five years. Depression and hypertension were frequent in HG. All HG patients had altered TSH values and 50 percent had diminished T4 values. Sensorineural hearing loss was detected in 22 ears from the HG and in seven from the CG. BERA was normal in the CG and altered in 10 ears from the HG, showing L-V increase. TOAEs were absent in 12 ears from the HG and in four from the CG. CONCLUSIONS: HG patients had more cochleovestibular symptoms, higher audiometric thresholds, increase in L-V in the BERA and absence or reduction in TOAEs amplitudes. Such alterations were not associated with THS and free T4 levels.