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1.
Neuroradiology ; 63(8): 1215-1225, 2021 Aug.
Artigo em Inglês | MEDLINE | ID: mdl-33459822

RESUMO

PURPOSE: Meningiomas are the most common extra-axial intracranial neoplasms with typical radiological findings. In approximately 2% of cases, histopathological reports reveal different neoplasms or non-neoplastic lesions that can closely mimic meningiomas. We describe radiological features of meningioma mimics highlighting imaging red flags to consider a differential diagnosis. METHODS: A total of 348 lesions with radiological diagnosis of meningiomas which underwent to surgical treatment or biopsy between December of 2000 and September of 2014 were analyzed. We determined imaging features that are not a typical finding of meningiomas, suggesting other lesions. The following imaging characteristics were evaluated on CT and MRI: (a) bone erosion; (b) hyperintensity on T2WI; (c) hypointensity on T2WI; (d) bone destruction; (e) dural tail; (f) leptomeningeal involvement; (g) pattern of contrast enhancement; (h) dural displacement sign. RESULTS: We have a relatively high prevalence of meningioma mimics (7.2%). Dural-based lesions with homogeneous contrast enhancement (52%) are easily misdiagnosed as meningiomas. Most lesions mimic convexity (37.5%) or parafalcine (21.9%) meningiomas. We have determined five imaging red flags that can alert radiologists to consider meningioma mimics: (1) bone erosion (22.2%); (2) dural displacement sign (36%); (3) marked T2 hypointensity (32%); (4) marked T2 hyperintensity (12%); (5) absence of dural tail (48%). The most common mimic lesion in our series was hemangiopericytomas, followed by lymphomas and schwannomas. CONCLUSION: The prevalence of meningioma mimics is not negligible. It is important to have awareness on main radiological findings suggestive of differential diagnosis due to a wide range of differentials which lead to different prognosis and treatment strategies.


Assuntos
Hemangiopericitoma , Neoplasias Meníngeas , Meningioma , Neurilemoma , Humanos , Imageamento por Ressonância Magnética , Neoplasias Meníngeas/diagnóstico por imagem , Meningioma/diagnóstico por imagem
2.
Clin Imaging ; 98: 26-35, 2023 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-36996597

RESUMO

Vasculitis is a complication of several infectious diseases affecting the central nervous system, which may result in ischemic and/or hemorrhagic stroke, transient ischemic attack, and aneurysm formation. The infectious agent may directly infect the endothelium, causing vasculitis, or indirectly affect the vessel wall through an immunological mechanism. The clinical manifestations of these complications usually overlap with those of non-infectious vascular diseases, making diagnosis challenging. Intracranial vessel wall magnetic resonance imaging (VWI) enables the evaluation of the vessel wall and the diseases that affect it, providing diagnostic data beyond luminal changes and enabling the identification of inflammatory changes in cerebral vasculitis. This technique demonstrates concentric vessel wall thickening and gadolinium enhancement, associated or not with adjacent brain parenchymal enhancement, in patients with vasculitis of any origin. It permits the detection of early alterations, even before a stenosis occurs. In this article, we review the intracranial vessel wall imaging features of infectious vasculitis of bacterial, viral, and fungal etiologies.


Assuntos
Doenças Transmissíveis , Vasculite do Sistema Nervoso Central , Humanos , Angiografia por Ressonância Magnética/métodos , Meios de Contraste , Angiografia Cerebral/métodos , Gadolínio , Imageamento por Ressonância Magnética , Vasculite do Sistema Nervoso Central/diagnóstico por imagem , Vasculite do Sistema Nervoso Central/patologia
3.
Clin Nucl Med ; 46(4): e198-e199, 2021 Apr 01.
Artigo em Inglês | MEDLINE | ID: mdl-33323727

RESUMO

ABSTRACT: A 57-year-old woman with a history of multiple sclerosis presented with a 5-day history of progressive headache and confusion, followed by left hemiparesis. The patient had stopped her previous fingolimod usage during the last 8 weeks. Brain MRI and 18F-FDG PET showed a subcortical tumefactive lesion with an intense peripheric rim of hypermetabolism and central hypometabolism, with central hyperintensity, thin isointense rim, and peripheral finger-like "tentacles" of edema with an irregular and thick border enhancement on postcontrast T2-weighted MRI. Brain biopsy showed features suggestive of relapsing MS. The patient improved after methylprednisone and plasma exchange.


Assuntos
Cloridrato de Fingolimode/farmacologia , Fluordesoxiglucose F18 , Imageamento por Ressonância Magnética , Esclerose Múltipla/diagnóstico por imagem , Esclerose Múltipla/metabolismo , Bainha de Mielina/metabolismo , Tomografia por Emissão de Pósitrons , Biópsia , Feminino , Humanos , Pessoa de Meia-Idade , Imagem Multimodal , Esclerose Múltipla/patologia , Recidiva , Suspensão de Tratamento
4.
Brain Dev ; 42(2): 211-216, 2020 Feb.
Artigo em Inglês | MEDLINE | ID: mdl-31677917

RESUMO

SCN3A was recently recognized as a gene associated with neurodevelopmental disorder and epilepsy. We present two additional patients with a novel de novo SCN3A pathogenic variant, and a review of all published cases of de novo variants. In one of our patients brain magnetic resonance imaging (MRI) disclosed a severe polymicrogyria and in the other it was normal. The clinical phenotype was characterized by a severe developmental delay and refractory epilepsy in the patient with polymicrogyria and intellectual disability with autistic features and pharmacoresponsive epilepsy in the subject with normal MRI. Polymicrogyria, a disorder of progenitor cells proliferation and migration, is an unanticipated finding for an ion channel dysfunction.


Assuntos
Canal de Sódio Disparado por Voltagem NAV1.3/genética , Transtornos do Neurodesenvolvimento/genética , Canais de Sódio/genética , Pré-Escolar , Epilepsia/genética , Feminino , Genótipo , Humanos , Deficiência Intelectual/genética , Imageamento por Ressonância Magnética , Masculino , Mutação/genética , Canal de Sódio Disparado por Voltagem NAV1.3/metabolismo , Transtornos do Neurodesenvolvimento/fisiopatologia , Fenótipo , Polimicrogiria/genética , Canais de Sódio/metabolismo
5.
Artigo em Inglês | MEDLINE | ID: mdl-29226021

RESUMO

Background: The development of Holmes tremor (HT) after a direct lesion of the midbrain has rarely been reported in the literature, although several etiologies have been linked with HT, such as stroke, brainstem tumors, multiple sclerosis, head trauma, or infections. Phenomenology Shown: A 31-year-old male, having been stabbed in the right eye, presented with a rest and action tremor in the left upper limb associated with left hemiparesis with corresponding post-contrast volumetric magnetic resonance imaging T1 with sagittal oblique reformation showing the knife trajectory reaching the right midbrain. Educational Value: Despite the rarity of the etiology of HT in the present case, clinicians working with persons with brain injuries should be aware of this type of situation.


Assuntos
Mesencéfalo/lesões , Tremor/etiologia , Ferimentos Perfurantes/complicações , Adulto , Traumatismos Oculares/complicações , Traumatismos Oculares/diagnóstico por imagem , Traumatismos Oculares/fisiopatologia , Humanos , Masculino , Mesencéfalo/diagnóstico por imagem , Mesencéfalo/fisiopatologia , Paresia/diagnóstico por imagem , Paresia/etiologia , Paresia/fisiopatologia , Tremor/diagnóstico por imagem , Tremor/tratamento farmacológico , Tremor/fisiopatologia , Ferimentos Perfurantes/diagnóstico por imagem , Ferimentos Perfurantes/fisiopatologia
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