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1.
J Stroke Cerebrovasc Dis ; 29(11): 105264, 2020 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-33066939

RESUMO

INTRODUCTION: Giant cavernomas (GCMs) are angiographically occult vascular malformations of the central nervous system measuring at least 4 cm in diameter. These are rare lesions, especially in the cerebellum. As such, the clinical and radiologic features, surgical management, and outcomes of treatment for this condition are unknown. METHODS: We performed a systematic review of SCOPUS and PubMed databases for case reports and case series of histopathologically proven GCMs arising from the cerebellum in the pediatric population, and included a case managed at our center. Data on clinical presentation, imaging features, surgical treatment and outcomes of management were collected. RESULTS: A total of 10 cases were identified from the systematic review, including our case report. The patients' median age was 6 months, with a slight male sex predilection (1.5:1). The most common neurologic manifestations were bulging fontanelle in infants, and headache and focal cerebellar deficits in older children. Surgical excision was done in all cases, while 50% of the cases had CSF diversion surgery done prior to excision. In cases with reported outcome, complete neurologic recovery was achieved in seven while partial recovery was reported in one case. No deaths were reported at median follow-up of 12 months. CONCLUSION: Our case report and systematic review show that giant cerebellar cavernoma is a rare differential diagnosis for symptomatic hemorrhagic cerebellar masses in the pediatric age group. Mainstay of treatment is surgical excision, which can be associated with favorable outcome in most cases.


Assuntos
Neoplasias Cerebelares , Hemangioma Cavernoso do Sistema Nervoso Central , Adolescente , Neoplasias Cerebelares/complicações , Neoplasias Cerebelares/diagnóstico por imagem , Neoplasias Cerebelares/patologia , Neoplasias Cerebelares/cirurgia , Craniotomia , Feminino , Hemangioma Cavernoso do Sistema Nervoso Central/complicações , Hemangioma Cavernoso do Sistema Nervoso Central/diagnóstico por imagem , Hemangioma Cavernoso do Sistema Nervoso Central/patologia , Hemangioma Cavernoso do Sistema Nervoso Central/cirurgia , Humanos , Lactente , Masculino , Recuperação de Função Fisiológica , Resultado do Tratamento , Carga Tumoral
3.
Neuroimaging Clin N Am ; 13(1): 27-40, 2003 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-12802939

RESUMO

Cavernous malformations are commonly being recognized on CT and MR imaging in both asymptomatic and symptomatic patients. The diagnosis of CMs can often be made on MR imaging based on the characteristic morphology of the subacute and chronic blood products. An atypical appearance of a CM in the setting of a recent hemorrhage requires follow-up imaging to confirm the diagnosis. Deep CMs have a significant clinical event rate that justifies close follow up or surgical treatment if possible.


Assuntos
Neoplasias Encefálicas/diagnóstico por imagem , Neoplasias Encefálicas/patologia , Transtornos Cerebrovasculares/diagnóstico por imagem , Transtornos Cerebrovasculares/patologia , Hemangioma Cavernoso do Sistema Nervoso Central/diagnóstico por imagem , Hemangioma Cavernoso do Sistema Nervoso Central/patologia , Adolescente , Adulto , Neoplasias Encefálicas/terapia , Transtornos Cerebrovasculares/terapia , Criança , Hemangioma Cavernoso do Sistema Nervoso Central/terapia , Humanos , Imageamento por Ressonância Magnética , Tomografia Computadorizada por Raios X
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