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1.
Surg Neurol Int ; 12: 25, 2021.
Artigo em Inglês | MEDLINE | ID: mdl-33598341

RESUMO

BACKGROUND: There are rare reports of broken surgical blades occurring during lumbar discectomy, and even fewer that discuss their retrieval. CASE DESCRIPTION: While a 54-year-old male was undergoing a lumbar discectomy, the knife blade was broken. As it was difficult to retrieve the fragment through the original incision, the patient was closed, and a postoperative angio-computerized tomography (CT) was obtained. When the CT angiogram (CTA) documented the retained fragment had become lodged near the iliac vein within the psoas muscle, a second operation for blade retrieval, consisting of a paravertebral, lateral transpsoas approach, was successfully performed. CONCLUSION: In some cases, it is difficult to retrieve a broken scalpel blade during the index surgery. When this occurs, we would recommend closing the patient, and obtaining a CTA to better document the location of the retained foreign body. Based upon these findings, a safer second stage procedure may be performed (e.g., as in this case using a paravertebral lateral transpsoas approach) to avoid undue sequelae/morbidity.

2.
Neurocirugia (Astur : Engl Ed) ; 30(4): 198-201, 2019.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-30060994

RESUMO

Pott's puffy tumour (PPT) is a rare entity that involves scalp swelling associated with subperiosteal abscess and cranial osteomyelitis, occasionally accompanied by intracranial infection. It is usually affiliated with frontal sinusitis, which is a typical but infrequent complication. On the contrary, Osteomyelitis by Actinomyces is rare and usually occurs at the mandibular level, with very few cases of cranial osteomyelitis caused by this bacterial specie, especially after traumatic brain injury. We report an exceptionally unusual case of a PPT frontal tumor after blunt trauma (closed head injury), with an intracranial lesion whereby Actinomyces was isolated after surgery, as a co-participant of the mentioned infection besides Fusobacterium and Propionibacterium.


Assuntos
Actinomyces/isolamento & purificação , Traumatismos Craniocerebrais/complicações , Fusobacterium/isolamento & purificação , Tumor de Pott/microbiologia , Propionibacterium/isolamento & purificação , Humanos , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Tumor de Pott/diagnóstico por imagem , Tumor de Pott/cirurgia , Tomografia Computadorizada por Raios X
4.
Arch Bronconeumol ; 49(11): 491-3, 2013 Nov.
Artigo em Inglês, Espanhol | MEDLINE | ID: mdl-23791243

RESUMO

Chondroid chordoma is an extremely rare tumour with an annual incidence of around 0.1 cases per 100,000population. Involvement of the thoracic vertebrae may be present in 2-5% of cases. Definitive diagnosis usually requires a suitable distinction between this and other mesenchymal tumours such as chondrosarcomas, so immunohistochemical analysis is virtually mandatory. In spite of its slow-growing nature, chondroid chordoma tends to relapse, and it may eventually become malignant, often jeopardising the patient's prognosis. Although surgery remains the main therapeutic approach, research into the molecular and genetic aspects of this tumour is ongoing. These new advances are likely to improve future oncology therapies by complementing surgery and radiotherapy, changing the currently poor prognosis. We report the case of a patient with a chondroid chordoma involving the thoracic vertebrae and pleural cavity, and the treatment performed.


Assuntos
Cordoma/diagnóstico , Cavidade Pleural/patologia , Neoplasias Torácicas/diagnóstico , Vértebras Torácicas/patologia , Antineoplásicos/uso terapêutico , Cordoma/diagnóstico por imagem , Cordoma/patologia , Cordoma/secundário , Cordoma/terapia , Terapia Combinada , Curetagem , Erros de Diagnóstico , Diafragma/patologia , Equinococose/diagnóstico , Receptores ErbB/antagonistas & inibidores , Humanos , Laminectomia , Imageamento por Ressonância Magnética , Masculino , Pessoa de Meia-Idade , Neoplasias Musculares/secundário , Invasividade Neoplásica , Proteínas de Neoplasias/antagonistas & inibidores , Cavidade Pleural/diagnóstico por imagem , Neoplasias Pleurais/secundário , Próteses e Implantes , Inibidores de Proteínas Quinases/uso terapêutico , Radioterapia Adjuvante , Indução de Remissão , Sarcoma/diagnóstico , Neoplasias Torácicas/diagnóstico por imagem , Neoplasias Torácicas/patologia , Neoplasias Torácicas/terapia , Vértebras Torácicas/diagnóstico por imagem , Tomografia Computadorizada por Raios X
5.
Neurocirugia (Astur) ; 24(5): 216-9, 2013.
Artigo em Espanhol | MEDLINE | ID: mdl-23453309

RESUMO

Idiopathic spinal cord herniation is a rare cause of thoracic myelopathy and its recurrence is even more infrequent. Cord herniation is through an anterior dural defect in thoracic spine with unknown causes. Symptomatic cases must be surgically treated to reduce the hernia and seal the defect to prevent recurrences. We report a patient presenting a Brown-Séquard syndrome secondary to a D5 spinal cord herniation treated successfully and its posterior traumatic recurrence.


Assuntos
Deslocamento do Disco Intervertebral/etiologia , Traumatismos da Medula Espinal/complicações , Feminino , Humanos , Pessoa de Meia-Idade , Recidiva
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