Comparison between different magnetic resonance sequences in the detection of calcifications in patients with neurocysticercosis

Introdução: Neurocisticercose (NCC) é a principal causa evitável de epilepsia adquirida no mundo. NCC, além de ser, a doença parasitária mais comum do SNC, representa um importante problema de saúde pública, especialmente em países em desenvolvimento. Estudos de neuroimagem são cruciais no diagnóstico e planejamento terapêutico da NCC. Apesar da ressonância magnética (RM) fornecer maior número e detalhe de informações sobre a doença, a tomografia computadorizada (TC) ainda é o método mais sensível na detecção de calcificação intracraniana, o achado radiológico mais comum da NCC. Objetivo: Comparar performance das sequências de RM ponderadas em suscetibilidade magnética na identificação de calcificações intracranianas em pacientes com NCC. Métodos: Estudo prospectivo, unicêntrico, no qual 57 indivíduos foram submetidos a TC e RM de crânio. Todos os indivíduos foram provenientes do Ambulatório de Doenças Infecciosas do Departamento de Neurologia do Hospital das Clínicas - Faculdade de Medicina da Universidade de São Paulo (HC-FMUSP), com diagnóstico confirmado de NCC. O protocolo de RM incluiu uma sequência convencional 2D gradiente eco (2D-GRE) e duas relativamente novas sequências de suscetibilidade magnética: susceptibilityweighted imaging (SWI) e principles of echo shifting with a train of observations (PRESTO). A TC foi considerada método padrão de referência. Dois neurorradiologistas, cegos para os dados clínicos e demais achados radiológicos, analisaram independentemente as sequências 2D-GRE, SWI e PRESTO quanto à presença, número e localizações de calcificações intracranianas atribuídas a NCC. Resultados: Foram identificadas, pela TC, 739 lesões calcificadas relacionadas a NCC em 50 dos 57 indivíduos incluídos no estudo. A média de lesões calcificadas por paciente foi de 12,9 (± 19,8). A médias de lesões encontradas pelas sequências de suscetibilidade magnética, obtido através da média dos resultados dos observadores, foi de 10,8 (± 17,5) para PRESTO, 10,6 (± 17,3) para SWI e 8,3 (± 13,6) para 2D-GRE. Neste quesito não houve diferença estaticamente significativa entre PRESTO e SWI (p = 0,359) e ambos foram superiores a 2D-GRE (p < 0,05). A concordância foi fraca a moderada, provavelmente devido ao alto número de lesões falso-positivas encontradas (490), das quais 53,9% representavam lesões relacionadas a NCC em estágios não calcificados. A sensibilidade e especificidade das sequências estudadas em identificar corretamente indivíduos com NCC em estágio calcificado foi respectivamente de 85% e 100% para 2D-GRE, 90% e 100% para SWI e 93% e 100% para PRESTO. Conclusão: As sequências SWI, PRESTO e 2D-GRE apresentam boa sensibilidade na identificação de lesões calcificadas em pacientes com NCC. As sequências SWI e PRESTO tiveram melhor performance do que 2D-GRE. Todas as sequências estudadas mostrarem-se apropriadas para identificar indivíduos com NCC no estágio de calcificação. Sequências ponderadas em suscetibilidade magnética podem ajudar no entendimento da história natural, fisiopatologia e achados de imagem da NCCBackground: Neurocysticercosis (NCC) is the main preventable cause of acquired epilepsy. NCC, besides being the most common parasitic disease of the CNS, is an important public health problem, mainly in developing countries. Neuroimaging studies are crucial in the diagnosis and therapeutic planning of NCC. Although magnetic resonance imaging (MRI) provides countless and more detailed information about the disease, computed tomography (CT) is still the most sensitive method for detecting intracranial calcification, the most common radiological finding of NCC. Purpose: To compare the diagnostic performance of susceptibility-weighted MRI sequences in identification of intracranial calcifications in patients with NCC. Methods: A prospective study with 57 subjects who underwent CT and MRI of the brain. All individuals came from Department of Neurology of the Hospital das Clínicas - Faculdade de Medicina da Universidade de São Paulo (HC-FMUSP), with a stablished diagnosis of NCC. The MRI protocol included a conventional 2D gradient echo sequence (2D-GRE) and two relatively new susceptibility-weighted sequences: susceptibility-weighted imaging (SWI) and principles of echo shifting with a train of observations (PRESTO). CT was considered the standard reference method. Two neuroradiologists, blinded to clinical data and other radiological findings, independently analyzed the 2D-GRE, SWI and PRESTO sequences on behalf to presence, number and sites of intracranial calcifications attributed to NCC. Results: A total of 739 NCC-related calcified lesions were identified by CT in 50 of the 57 subjects included in the study. The mean number of calcified lesions per patient was 12.9 (± 19.8). The mean number of lesions found by the susceptibility-weighted MRI sequences, obtained through the mean of the observers\' results, was 10.8 (± 17.5) for PRESTO, 10.6 (± 17.3) for SWI and 8.3 (± 13.6) for 2D-GRE. There was no statistically significant difference between PRESTO and SWI (p = 0.359) and both were superior to 2D-GRE (p < 0.05). The concordance was weak to moderate, probably due to the high number of false-positive lesions found (490), of which 53.9% represented NCC-related lesions in non-calcified stages. The sensitivity and specificity of the sequences studied in correctly identifying individuals with calcified NCC were 85% and 100% respectively for 2D-GRE, 90% and 100% for SWI and 93% and 100% for PRESTO. Conclusion: SWI, PRESTO and 2D-GRE sequences have good sensitivity in the identification of calcified lesions in patients with NCC. SWI and PRESTO performed better than 2DGRE. All sequences studied are suitable for identifying individuals with NCC in the calcified stage. The new susceptibility-weighted MRI sequences may help in understanding the natural history, pathophysiology and imaging findings of NC

Acquired hepatocerebral degeneration: a case report

ABSTRACT Acquired hepatocerebral degeneration is an underdiagnosed neurologic syndrome characterized by parkinsonism, ataxia or other movement disorders and by neuropsychiatric and cognitive symptoms. It occurs in patients with chronic liver disease, especially those who develop portosystemic shunting and is often unrecognized as a cause of cognitive decline. Recently, its pathogenesis has been associated with manganese accumulation in basal ganglia and some treatments proposed. The aim of this article was to report a case and discuss some discoveries in connection with the disease

Adult-onset adrenoleukodystrophy presenting as a psychiatric disorder: MRI findings

ABSTRACT A 35-year-old, previously healthy man presented psychiatric symptoms lasting four years, receiving treatment with neuroleptics. One year later he evolved with gait disequilibrium. After a further six months, cognitive symptoms were characterized with rapid evolution to a profound demented state. MRI showed signal changes in cerebral white matter and very long-chain fatty acids were detected in blood

Reversible dementia due to Neurocysticercosis: improvement of the racemose type with antihistamines

Infection of the human central nervous system (CNS) by the larvae of Taenia solium, termed neurocysticercosis (NCC), is endemic in most developing countries, where it is a major cause of acquired seizures and other neurological morbidity, including neuropsychiatric symptoms. However, despite its frequent manifestation, some findings, such as cognitive impairment and dementia, remain poorly understood. Less commonly, NCC may affect the ventricular system and subarachnoid spaces and this form is known as extraparenchymal neurocysticercosis. A particular presentation of the subarachnoid form is called racemose cysticercosis, which has a progressive pattern, frequently leads to hydrocephalus and can be life-threatening. Here we review a case of the racemose variety of cysticercosis, complicated by hydrocephalus and reversible dementia, with remission of symptoms after derivation and that remained stable with use of dexchlorpheniramine. We discuss the challenges in diagnosis, imaging findings, treatment and follow-up of this disease

Progressive posterior cortical dysfunction

Abstract Progressive posterior cortical dysfunction (PPCD) is an insidious syndrome characterized by prominent disorders of higher visual processing. It affects both dorsal (occipito-parietal) and ventral (occipito-temporal) pathways, disturbing visuospatial processing and visual recognition, respectively. We report a case of a 67-year-old woman presenting with progressive impairment of visual functions. Neurologic examination showed agraphia, alexia, hemispatial neglect (left side visual extinction), complete Balint's syndrome and visual agnosia. Magnetic resonance imaging showed circumscribed atrophy involving the bilateral parieto-occipital regions, slightly more predominant to the right . Our aim was to describe a case of this syndrome, to present a video showing the main abnormalities, and to discuss this unusual presentation of dementia. We believe this article can contribute by improving the recognition of PPCD

The &quot;eye sign&quot; due to hemispatial neglect A case report

Abstract -Conjugate eye deviation is characterized by a sustained shift in horizontal gaze, usually toward the affected brain hemisphere. When detected on neuroimaging, it is called the &quot;eye sign&quot;. It is classically associated with lesions involving the frontal eye fields, ipsilateral to the side of the deviation. Neglect may be conceptualized as a spatially addressed bias of the sensory events in explicit behaviors and in the absence of perceptual and motor deficits. Hemispatial neglect is a common disabling condition that occurs following acute unilateral brain damage, usually to the right side. We report a case of a patient presenting with the &quot;eye sign&quot; on tomography, following an acute subinsular stroke, in the absence of conjugated eyes deviation. Our hypothesis was that the sign may have been due to hemispatial neglect in this patient. The aim of this article was to discuss the mechanisms involved in the attention network and its neuroanatomic correlates. Key words: hemispatial neglect, insular stroke, conjugate eye deviation, &quot;eye sign&quot;. &quot;Sinal do olhar&quot; por negligência hemiespacial: um relato de caso Resumo -Desvio conjugado do olhar é caracterizado por um desvio sustentado horizontal da mirada, normalmente para o lado do hemisfério afetado. Quando visto por métodos de imagem, é chamado &quot;sinal do olhar&quot;. O sinal é normalmente associado a lesões envolvendo o &quot;campo frontal do olho&quot; ipsilateral ao lado do desvio. Negligência pode ser conceitualizada como um viés espacial dos eventos sensoriais no comportamento explícito, na ausência de alterações da percepção e motoras. Negligência hemiespacial é uma condição comum e incapacitante que ocorre após lesão cerebral aguda, principalmente à direita. Nós relatamos um caso de um paciente que apresenta o &quot;sinal do olhar&quot; na tomografia, após um infarto subinsular, na ausência de desvio conjugado do olhar. Nossa hipótese é que, neste paciente, o sinal pode ser devido à negligência hemiespacial. O objetivo deste artigo é discutir os mecanismos envolvidos na rede da atenção e seus correlatos anatômicos. Palavras-chave: negligência hemiespacial, infarto insular, desvio conjugado do olhar, &quot;sinal do olhar&quot;