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1.
J Neurosurg Case Lessons ; 2(18): CASE21268, 2021 Nov 01.
Artigo em Inglês | MEDLINE | ID: mdl-36061626

RESUMO

BACKGROUND: Sectioning the C2 nerve root is increasingly utilized during posterior C1-2 fusion, as the nerve overlies the entry point for C1 lateral mass screws and the C1-2 joint. Nerve sectioning improves visualization for screw placement and enables joint decortication for arthrodesis. While rare, vascular injury is a devastating complication of atlantoaxial fusion. Anomalous vascular anatomy at C1-2 greatly increases risk of iatrogenic injury. OBSERVATIONS: A 78-year-old female with rheumatoid arthritis and prior C2-7 fusion presented with myelopathy from a compressive pannus at C1-2. She underwent C1 laminectomy and C1-2 posterior instrumented fusion. Intraoperatively, arterial bleeding occurred as the right C2 nerve root was sectioned. Vertebral artery injury was suspected, and tamponade was performed while vascular control was established. The artery passed aberrantly beneath the nerve root in the C1-2 foramen. It was repaired microsurgically, and patency was confirmed using indocyanine green. The remainder of the fusion was aborted. The patient wore a cervical collar and was treated with aspirin for 6 weeks before undergoing instrumented fusion. The patient suffered no deficits. LESSONS: Although rare, anomalous vertebral artery anatomy increases risk of injury at time of C2 nerve root sectioning. Preoperative assessment of the vasculature is vital.

2.
CNS Oncol ; 7(4): CNS25, 2018 12 01.
Artigo em Inglês | MEDLINE | ID: mdl-30543115

RESUMO

BACKGROUND: Transformation to glioblastoma following recurrent epidermoid cyst resection has not been reported. Chronic inflammation can underlie malignant transformation of epidermoid cysts. Astrogliosis following repeated resections may have induced the rare transformation to glioblastoma. CLINICAL PRESENTATION: A patient presenting with left lower extremity weakness was found to harbor a parietal mass lesion. Histopathology demonstrated an epidermoid cyst. Following multiple re-resections, an intra-axial mass was discovered within the operative bed, confirmed as glioblastoma. CONCLUSION: This is the first report of glioblastoma associated with a resected epidermoid cyst. Subsequent to resection, the chronic inflammatory milieu propagated by astrogliosis is thought to have induced malignancy. The progression to glioblastoma draws attention to neoplastic transformation in the context of recurrent epidermoids.


Assuntos
Encefalopatias/fisiopatologia , Cisto Epidérmico/fisiopatologia , Glioblastoma/fisiopatologia , Encefalopatias/diagnóstico por imagem , Encefalopatias/patologia , Encefalopatias/cirurgia , Progressão da Doença , Cisto Epidérmico/diagnóstico por imagem , Cisto Epidérmico/patologia , Cisto Epidérmico/cirurgia , Evolução Fatal , Feminino , Glioblastoma/diagnóstico por imagem , Glioblastoma/patologia , Glioblastoma/terapia , Humanos , Pessoa de Meia-Idade
4.
J Neurosurg Pediatr ; 20(6): 521-525, 2017 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-28937919

RESUMO

The authors describe the case of a patient with the classic clinical presentation and radiographic features of a nasal dermal sinus with an associated intracranial cyst; however, histopathology revealed that the intracranial cyst was neurenteric instead of the typical epidermoid or dermoid cyst. Preoperative assessment included CT and MRI, which revealed a direct communication between the patient's nasal polypoid lesion and the anterior skull base via the foramen cecum. At the hands of a multidisciplinary plastic surgery and neurosurgery team, the patient underwent concurrent gross-total resection of the nasal polypoid lesion, the intracranial intradural cystic lesion, and their interconnecting tract.


Assuntos
Gerenciamento Clínico , Defeitos do Tubo Neural/diagnóstico por imagem , Defeitos do Tubo Neural/cirurgia , Seios Paranasais/diagnóstico por imagem , Seios Paranasais/cirurgia , Pré-Escolar , Feminino , Humanos , Procedimentos Neurocirúrgicos/métodos
5.
Clin Infect Dis ; 34(10): 1323-30, 2002 May 15.
Artigo em Inglês | MEDLINE | ID: mdl-11981727

RESUMO

To test the hypothesis that the infecting meningococcal serogroup modulates the presentation, course, and outcome of invasive meningococcal disease (IMD), we performed a retrospective review of cases of IMD in 407 children from 2 tertiary referral centers and 2 regional centers in Ireland. Patients infected with serogroup C meningococci (n=104) were older than those infected with serogroup B (n=303; median, 2.5 vs. 1.5 years; P=.04); all other demographic and clinical parameters were similar for the 2 groups. Among serogroup B patients, mortality was 3.6% and morbidity was 10%; for serogroup C patients, mortality was 4.8% and morbidity was 12.5% (P=.81 and P=.76, respectively). Serogroup C-associated sequelae more often were multiple (P=.003). Despite the introduction of serogroup C conjugate vaccine into the routine immunization schedule of some countries, ongoing morbidity from IMD is anticipated, because group B disease was very similar to group C disease in this pediatric population.


Assuntos
Infecções Meningocócicas/fisiopatologia , Adolescente , Criança , Pré-Escolar , Humanos , Lactente , Recém-Nascido , Irlanda/epidemiologia , Infecções Meningocócicas/epidemiologia , Infecções Meningocócicas/imunologia , Infecções Meningocócicas/mortalidade , Sorotipagem
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