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1.
Otolaryngol Clin North Am ; 56(5): 909-918, 2023 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-37553272

RESUMO

Fungal infections of the external auditory canal can range from common (otomycosis) to life threatening (necrotizing otitis externa). Proper identification of fungal pathogens is necessary to guide appropriate therapy, and a high index of suspicion for fungal causes of ear canal disease is critical. Fungal pathogens may be an especially important cause of ear canal disease in certain populations, including patients with diabetes, patients recently treated with antibiotics, and immunosuppressed patients. Opportunistic fungal infections of the ear canal are an emerging concern.


Assuntos
Otopatias , Micoses , Otite Externa , Humanos , Meato Acústico Externo , Otite Externa/diagnóstico , Otite Externa/terapia , Otite Externa/etiologia , Micoses/diagnóstico , Micoses/terapia , Micoses/complicações , Antibacterianos
2.
Int J Pediatr Otorhinolaryngol ; 131: 109868, 2020 Apr.
Artigo em Inglês | MEDLINE | ID: mdl-31931391

RESUMO

OBJECTIVES: Congenital encephaloceles provide unique diagnostic and reconstructive challenges for the pediatric rhinologist. The objectives of the current study were to evaluate contemporary treatment strategies for congenital encephaloceles focusing on presentation, surgical technique, and outcomes. METHODS: Multi-institutional retrospective chart review of congenital encephaloceles (2003-2019). Data regarding demographics, presenting symptoms, associated abnormalities, surgical technique, size, location, and complications were collected. RESULTS: Fourteen patients with 15 congenital encephaloceles were treated using endoscopic techniques (avg 6.0 years, range 2 months-22 years) with mean follow up of 23 months. The majority presented with nasal obstruction (n = 13); only one child had cerebrospinal fluid (CSF) rhinorrhea. Associated anomalies included nasal deformities, congenital hypopituitarism, and Morning Glory syndrome. Average encephalocele size was 2.44 cm (range 0.5-3.6 cm) with mean skull base defect size of 8.6 x 7.7 mm. Locations included the foramen cecum (n = 9), central sphenoid (n = 3), midline anterior cranial fossa (n = 1), orbital plate of frontal bone (n = 1), and ethmoid roof (n = 1). Because of favorable expansion from encephaloceles, it was unnecessary to postpone surgeries to allow nasal cavity growth. Three individuals had prior operations, including surgeries for "nasal polyp" or "adenoid cyst". Two patients had post-operative complications (meningitis and CSF leak) effectively treated with no further sequelae. CONCLUSIONS: In the current study, congenital encephaloceles in children as young as 2 months were successfully repaired using endoscopic techniques. Endoscopic approaches remain a safe and effective intervention for management of these lesions.


Assuntos
Encefalocele/congênito , Encefalocele/cirurgia , Endoscopia , Complicações Pós-Operatórias/epidemiologia , Base do Crânio/anormalidades , Adolescente , Criança , Pré-Escolar , Encefalocele/diagnóstico , Feminino , Humanos , Lactente , Masculino , Seleção de Pacientes , Estudos Retrospectivos , Base do Crânio/cirurgia , Resultado do Tratamento , Adulto Jovem
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