Evaluación del método de ELISA para detección de anticuerpos anti-cisticercos en sueros humanos / Evaluation of the ELISA method for the detection of anti-cysticercus antibodies in human sera / Avaliação do método ELISA para a detecção de anticorpos anti-cisticercos em soros humanos

La neurocisticercosis (NCC) es la localización en el sistema nervioso central (SNC) humano de la parasitosis provocada por el estadio larvario de la Taenia solium, el cisticerco, que prevalece en áreas urbanas y rurales y constituye un problema de salud pública. El diagnóstico puede efectuarse por exploración imagenológica del SNC con resonancia magnética o tomografía axial computarizada, no siempre disponible, y por pruebas de inmunoensayo (EIA) en sangre, que aportan al diagnóstico rapidez, bajo costo y transferibilidad. Para evaluar su capacidad diagnóstica y validar la precisión de la técnica de ELISA (ensayo inmunoabsorbente ligado a enzimas), en la detección de anticuerpos anti-cisticercos en sueros humanos, se diseñó una seroteca en forma aleatoria y en doble ciego, y se realizó el ELISA con las muestras, utilizando placas sensibilizadas con antígenos obtenidos del fluido vesicular de cisticercos de T. solium. Para la validación se realizaron 20 ensayos empleando controles positivos y negativos, por cuadruplicado en diferentes días, y realizados por más de un operador; el punto de corte para este método fue una densidad óptica de 0,325. La precisión intralaboratorio para el control débil (media=0,532±0,09) fue de %CV=17,51±0,09, y un valor de repetibilidad de %CV=7,04±0,04, cifras que se encuentran dentro de los límites esperados para el método. Con estos resultados se puede concluir que la precisión del ELISA para el serodiagnóstico de NCC se encuentra validada. El ensayo validado proporcionó resultados coherentes y repetidos que permitieron discriminar entre dos resultados dicotómicos y establecer con exactitud la condición de una posible infección, con un nivel de certidumbre estadística predeterminado.

Neurocysticercosis (NCC) is the location in the human central nervous system (CNS) of the parasitosis caused by the larval stage of Taenia solium, the cysticercus which prevails in urban and rural areas, constituting a public health problem. Diagnosis can be made by CNS imaging with magnetic resonance or computerized axial tomography, not always available, and by blood immunoassay (EIA) tests, which provide rapidity, low cost and transferability. In order to evaluate its diagnostic capacity and validate the ELISA (Enzyme- Linked ImmunoSorbent Assay) technique in the detection of anti-cysticercus antibodies in human sera, a collection of sera was designed in a randomized and double-blind manner, and the ELISA was performed with the samples, using plates sensitized with antigens obtained from the vesicular fluid of T. solium cysticerci. Twenty trials were conducted, using positive and negative controls, in quadruplicate, on different days, and performed by more than one operator; the cutoff for this method was an optical density of 0.325. The intralaboratory precision for the weak control (mean=0.532±0.09) was %CV=17.51±0.09, and a repeatability value of %CV=7.04±0.04, figures that are within the expected limits for the method, It can be concludedthat the accuracy of the ELISA for serodiagnosis of NCC is validated. The validated test provided consistent and repeated results, which made it possible to discriminate between two dichotomous outcomes, and to establish with accuracy the condition of a possible infection, with a predetermined level of statistical certainty.

A neurocisticercose (NCC) é o local no sistema nervoso central (SNC) humano de parasitose causada pelo estágio larval da Taenia solium, o cisticerco, prevalecente em áreas urbanas e rurais, constituindo um problema de saúde pública. O diagnóstico pode ser feito por varredura imagenológica do SNC com ressonância magnética ou tomografia axial computadorizada, nem sempre disponível, e por testes de imunoensaio (EIA) em sangue, que fornecem ao diagnóstico rapidez, baixo custo e portabilidade. Para avaliar a sua capacidade de diagnóstico e validar a precisão da técnica de ELISA (ensaio imunoabsorvente ligado a enzimas), na detecção de anticorpos anti-cisticercos em soros humanos, um serrarium foi projetado em forma aleatória e em duplo cego, e foi realizado com as amostras o ELISA, utilizando placas sensibilizadas com antígenos derivados do fluido vesicular de cisticercos de T. solium. 20 testes para validação foram realizados, utilizando controles positivos e negativos, em quadruplicado, em dias diferentes, e realizados por mais de um operador; o ponto de corte para este método era uma densidade óptica de 0,325. A precisão intralaboratorial para o controle fraco (média=0,532±0,09) foi de CV%=17,51±0,09, e um valor de repetibilidade de CV%=7,04±0,04, valores que estão dentro dos limites esperados para o método, podendo concluir com esses resultados que a precisão do ELISA para diagnóstico sorológico de NCC é validado. O ensaio validado forneceu resultados consistentes e repetidos, o que permitiu discriminar entre dois resultados dicotômicos e identificar com exatidão a condição de possível infecção com um nível de certeza pré-determinado estatisticamente.

Assessment of impediments affecting health systems response to neurocysticercosis in two districts (Gulu and Amuru) of Northern Uganda: A cross sectional study

Northern Uganda is recovering from the effects of prolonged war which devastated most of the health systems in the region. The aim of the study was to identify health sector impediments affecting health systems response to Neurocysticercosis in the districts of Gulu and Amuru. A cross sectional study was conducted on two hospitals and 10 health centers. Two hundred and three (n=203) respondents were involved. Questionnaires were used to collect the data. One hundred and forty two (70.0%) of the respondents are permanently employed (P=0.01). Seventy three point nine percent (73.9%) of respondents are residents from Gulu districts (P=0.024). One hundred and nine (53.4%) of respondents reported they received training on infectious diseases (P=0.507). One hundred and forty three (70%) reported their health facilities have polices (P=0.04). One hundred and forty seven (72.4%) reported in-charges reside at health facilities (P=0.01). One hundred and twenty four (61%) of the respondents reported Government is the primary source of funding (P=0.02). One hundred and seventeen (57.6%) of the respondents reported funding are irregular (P=0.23). Eighty seven percent (87%) reported inadequate physical infrastructure (P=0.04). Seventy three point six have limited knowledge on the diagnosis of Neurocysticercosis (P=0.01) and many prescribe anti-helminthic drugs to patients (P=0.27). Despite improvement in the healthcare services in the health sectors, health systems response to Neurocysticercosis in Gulu and Amuru, Northern Uganda is weak with most health facilities operating minimally. There is need for holistic approach to improvement of health systems in the region through increased Government funding and advocacy

Diagnóstico y tratamiento en un caso de neurocisticercosis / Diagnosis and treatment of a neurocysticercosis case

La neurocisticercosis es una enfermedad del sistema nervioso central de origen parasitario que genera una alta morbilidad. Presentamos el caso de un paciente de 30 años de edad, negro, del sexo masculino, con historia de dolor de cabeza y disminución progresiva de la visión desde hace tres meses. Fue examinado en la Consulta de Oftalmología, donde se constató la pérdida visual y alteraciones campimétricas. En el fondo de ojo se observó papiledema bilateral. Le fue indicada tomografía computarizada de cráneo que mostró una gran lesión en la región frontal derecha y por lo cual fue transferido para el Servicio de Neurocirugía. Se decidió el tratamiento quirúrgico y se le realizó una craneotomía frontal derecha y resección de la lesión. El diagnóstico histológico confirmó una neurocisticercosis, por lo que se decidió comenzar el tratamiento con albendazol y praziquantel. El paciente evolucionó satisfactoriamente. Después de completar el tratamiento y pasados unos meses se le realizó la tomografía axial computarizada de control, donde se mostró una remisión total de la lesión(AU)

Neurocysticercosis is a disease of the central nervous system of parasitic origin and high morbidity. This is the case of a 30 years-old Black male patient with a history of headache and progressive reduction of vision for three months. He was examined at the Ophthalmological Service where visual loss and campometric alterations were confirmed. The fundus oculi revealed the presence of bilateral papilledema. He was performed cranial CT that showed a large lesion in the right front region, so he was transferred to the neurosurgery service. It was decided to apply surgical treatment. He was then performed a right front craniotomy and then resection of the lesion. The histological diagnosis confirmed neurocysticercosis and he was then treated with albendazol and praziquantel. His recovery was satisfactory. Upon completing the treatment and after a few months, the axial computerized tomography for control showed total remission of lesion(AU)

Evolución clínica de niño angolano con neurocisticercosis tratado en Cuba / Clinical evolution of an Angolan child with neurocysticercosis treated in Cuba

Introducción: se presenta por primera vez en el hospital un caso de neurocisticercosis. En el pasado era una enfermedad que solo ocurría en países en vías de desarrollo, ahora está apareciendo con mayor frecuencia en países desarrollados como Estados Unidos, Canadá y el Reino Unido. Es una enfermedad seria, en algunos casos puede ser mortal, aunque generalmente se puede prevenir y controlar. Se identifica un caso complejo no habitual en Cuba. Presentación del caso: paciente angolano, de 9 años de edad, con antecedentes de salud, que hace 2 meses en su país presentó un cuadro de fiebre, vómitos, convulsiones, hiperestesia y somnolencia. Posteriormente comenzó con trastorno de la conciencia dado por cuadro confusional, crisis epiléptica tónico clónicas generalizadas, y es enviado a Cuba a descartar tumor o absceso cerebral. Conclusiones: en el paciente evaluado hubo manifestaciones clínicas que podían responder a varias enfermedades neurológicas, pero los antecedentes epidemiológicos, los hallazgos en la resonancia magnética y la respuesta inmediata ante los antiparasitarios, resultaron definitivos para el diagnóstico de neurocisticercosis(AU)

Introduction: a case of neurocysticercosis is presented for the first time in the hospital. In the past it was a disease that only occurred in developing countries, now it is appearing more frequently in developed countries such as the United States, Canada and the United Kingdom. It is a serious disease, in some cases it can be fatal, although it can usually be prevented and controlled. A complex case, not usual in Cuba is identified. Case presentation: Angolan patient, 9 years old, with health history, whom 2 months ago in his country presented symptoms of fever, vomiting, seizures, hyperesthesia and drowsiness. Later, he presented a disorder of consciousness due to confusional symptoms, generalized tonic-clonic epileptic crisis, and he was sent to Cuba to rule out a tumor or brain abscess. Conclusions: in the evaluated patient there were clinical manifestations that could respond to several neurological diseases, but the epidemiological antecedents, the findings in the magnetic resonance and the immediate response to the antiparasitic drugs were crucial for the diagnosis of neurocysticercosis(AU)

Surgical treatment of neurocysticercosis. Retrospective cohort study and an illustrative case report / Tratamento cirúrgico da neurocisticercose. Estudo de coorte retrospectivo e um caso ilustrativo

ABSTRACT CONTEXT AND OBJECTIVE: Neurocysticercosis is prevalent in developing countries and manifests with several neurological signs and symptoms that may be fatal. The cysts may be parenchymal or extraparenchymal and therefore several signs and symptoms may occur. Depending on their location, neurosurgical procedures may be required, sometimes as emergencies. The aim here was to review 10-year statistics on all surgical neurocysticercosis cases at a large public tertiary-level hospital. DESIGN AND SETTING: Retrospective cohort at a large public tertiary-level hospital. METHODS: All surgical neurocysticercosis cases seen between July 2006 and July 2016 were reviewed. Parenchymal and extraparenchymal forms were considered, along with every type of surgical procedure (shunt, endoscopic third ventriculostomy and craniotomy). The literature was reviewed through PubMed, using the terms “neurocysticercosis”, “surgery”, “shunt” and “hydrocephalus”. RESULTS: 37 patients underwent neurosurgical procedures during the study period. Most were male (62.16%) and extraparenchymal cases predominated (81%). Patients aged 41 to 50 years were most affected (35.13%) and those 20 years or under were unaffected. Ventricular forms were most frequently associated with hydrocephalus and required permanent shunts in most cases (56.57%). CONCLUSIONS: The treatment of neurocysticercosis depends on the impairment: the parenchymal type usually does not require surgery, which is more common in the extraparenchymal form. Hydrocephalus is a frequent complication because the cysts often obstruct the cerebrospinal flow. The cysts should be removed whenever possible, to avoid the need for permanent shunts.

RESUMO CONTEXTO E OBJETIVO: A neurocisticercose é prevalente em países em desenvolvimento e manifesta-se com vários sinais e sintomas neurológicos que podem ser fatais. Os cistos podem ser parenquimatosos ou extraparenquimatosos, portanto vários sinais e sintomas podem estar presentes. Dependendo da sua localização, procedimentos neurocirúrgicos podem ser necessários, às vezes em caráter emergencial. O objetivo foi revisar dados estatísticos de um período de 10 anos de todos os casos cirúrgicos de neurocisticercose num grande hospital público terciário. TIPO DE ESTUDO E LOCAL: Coorte retrospectiva de um grande hospital público terciário. MÉTODOS: Todos os casos cirúrgicos de neurocisticercose de pacientes tratados entre julho 2006 e julho 2016 foram revisados. As formas parenquimatosas e extraparenquimatosas foram consideradas, assim como tipo de procedimento cirúrgico (derivação, terceiroventriculostomia endoscópica e craniotomia). A literatura foi revisada por meio da PubMed, utilizando-se os termos “neurocysticercosis”, “surgery”, “shunt” e “hydrocephalus”. RESULTADOS: 37 pacientes foram submetidos a procedimentos neurocirúrgicos nesse período, a maioria do sexo masculino (62.16%%) e casos extraparenquimatosos predominaram (81%). Pacientes com idade 41-50 anos foram os mais afetados (35,13%) e aqueles com 20 anos ou menos não foram afetados. As formas ventriculares mais frequentemente estiveram associadas a hidrocefalia e necessitaram da realização de shunts definitivos na maior parte dos casos (56,57%). CONCLUSÕES: O tratamento depende da forma de acometimento: o tipo parenquimatoso usualmente não necessita de cirurgia que é mais comum na forma extraparenquimatosa. Hidrocefalia é uma complicação frequente pois muitas vezes os cistos obstruem o fluxo liquórico. A remoção dos cistos deve ser realizada sempre que possível para evitar a necessidade de derivações definitivas.

Neuropsychiatric manifestations and epidemiology of neurocysticercosis / Manifestações neuropsiquiátricas e epidemiologia de neurocisticercose

Neurocysticercosis (NCC) is the brain infection caused by larval stages of the helminth Taenia solium. The embryos of Taenia travel through the bloodstream and can reach the brain, muscles, eyes, and various organs. In the brain, the psychiatric manifestations are mood disorders, depression and anxiety, which are commonly associated with epilepsy and sensory-motor deficits. Neurocysticercosis is a frequent parasitic disease in the world population; it is endemic in Central and South America, Asia and Sub-Saharan Africa. In the present review, we report the major symptoms and signals of neurocysticercosis common to neurological and psychiatric illnesses. We briefly present Epidemiology of those manifestations and analyze the relationship between pathological changes and NCC symptomatology. OBJECTIVES AND METHODOLOGY: A literature review was conducted to characterize epidemiological, neurological and psychiatric manifestations of NCC. The final 90 papers were selected of a set of 937 publications from 2010 to 2016. RESULTS: NCC is a major cause of epilepsy in endemic areas; further- more, leads to a diversity of motor and sensitive deficits, manifestations vary from headache to severe intracranial hypertension. Potentially fatal conditions include arteritis, encephalitis and hydrocephalus. Depression and cognitive decline remain among the most important psychiatric manifestations. Neuropsychiatric manifestations, Epidemiology, and neuroimaging provide diagnostic criteria. Brain scans may reveal one or diverse cysts filled with fluid within a scolex (parasite's head). CONCLUSION: NCC's diversity of presentations encourage health professionals to consider it in diagnoses, especially in endemic countries, and also in non-endemic areas because migrants and travelers are subject to contagious. Treatment consists in use of antiparasitic drugs (albendazol, praziquantel) and drugs to treat associated conditions (anticonvulsants, corticosteroids). Surgery is reserved to extirpate the parasite from particular locations (eyes, spinal cord, cerebral ventricles) or to differentiate NCC from tumors, tuberculosis, mycosis, etc. Prevention includes treatment of intestinal helminthiasis, sanitation in animal farming, food preparing hygiene, quality control of water and food.

Neurocisticercose é a infecção cerebral causada pelos estágios lar- vais do helminto Taenia solium. Os embriões da Taenia deslocam-se através da corrente sanguínea e podem atingir o cérebro, músculos, olhos e vários órgãos. No cérebro, as manifestações psiquiátricas são transtornos de humor, depressão e ansiedade, as quais estão comumente associados com epilepsia e deficiências sensório-motoras. Neurocisticercose é uma parasitose frequente na população mundial, é endêmica na América Central e do Sul, Ásia e África subsaariana. Na presente revisão, relatamos os principais sintomas e sinais de neurocisticercose pertinentes a doenças neurológicas e psiquiátricas. Nós brevemente apresentamos a Epidemiologia dessas manifestações, e analisamos a relação entre alterações patológicas e sintomatologia da NCC. OBJETIVOS E METODOLOGIA: Uma revisão da literatura foi conduzida para caracterizar a epidemiologia, as manifestações neurológicas e psiquiátricas de NCC. Os 90 artigos finais foram selecionados de um conjunto de 937 publicações entre 2010 a 2016. RESULTADOS: NCC é uma importante etiologia de epilepsia em áreas endêmicas, além disso causa uma diversidade de deficiências motoras e sensoriais, as manifestações variam de cefaleia a severa hipertensão intracraniana. Condições potencialmente fatais incluem arterites, encefalites e hidrocefalia. Depressão e declíneo cognitive permanecem entre as mais importantes manifestações psiquiátricas. Manifestações neuropsiquiátricas, epidemiologia e neuroimagem provêm os critérios de diagnóstico. As imagens cerebrais podem revelar um ou diversos cistos preenchidos com líquido e o escólex (cabeça) do parasito. CONCLUSÕES: A diversidade de apresentações da NCC encoraja os profissionais de saúde a considerá-la dentre os diagnósticos, especialmente em países endêmicos; e também em áreas não-endêmicas, pois migrantes e viajantes estão sujeitos ao contágio. O tratamento consiste no uso de antiparasíticos (albendazol, praziquantel) e medicamentos para tratar condições associadas (anticonvulsivantes, corticosteróides). Cirurgia é reservada para remoção do parasito de locais particulares (olhos, medula espinhal, ventrículos cerebrais) ou para diferenciar NCC de tumores, tuberculose, micose, etc. Prevenção inclui o tratamento de helmintíases intestinais, sanidade animal, higiene ao preparar alimentos, controle da qualidade da água e alimentos.

Spinal Neurocysticercosis: A Rare Variant of a Common Parasitic Infection

Neurocysticercosis is the most common parasitic infection affecting the central nervous system, usually involving the brain parenchyma, intracranial subarachnoid space, or ventricular system. In rare cases, there is involvement of the spine (vertebral, epidural, subdural, arachnoid, or intramedullary). Even in endemic regions, this variant is rare, with an incidence below 5% of all patients. The diagnosis is made based on the symptoms, which can be very unspecific, imaging and CSF analysis, with biopsy as a possibility. Treatment is usually curative, but important deficits can develop, due to compression of the spinal cord or nerve roots, arachnoiditis, or meningitis. We present the case of a patient who developed this entity, with poor clinical scenario, and review the literature on the topic.

Neurocisticercose é a infecção parasitária mais comum afetando o sistema nervoso central, geralmente envolvendo o parênquima cerebral, espaço subaracnóide intracraniano ou sistema ventricular. Em raros casos, há envolvimento da coluna vertebral, espaços epidural e subdural, aracnoide, ou intramedular. Mesmo em áreas endêmicas, esta variante é rara, com incidência abaixo de 5% entre todos os pacientes. O diagnóstico é feito com base nos sintomas, que podem ser bastante inespecíficos, neuroimagem e análise do líquor, sendo a biópsia uma possibilidade. O tratamento geralmente é curativo, porém importantes déficits podem se desenvolver, devido à compressão da medula espinhal ou raízes nervosas, aracnoidite ou meningite. Relatamos o caso de um paciente que desenvolveu esta entidade, com sintomatologia escassa, e revisamos a literatura sobre este tópico.

Validez de tres métodos de inmuno-diagnóstico de neurocisticercosis: revisión sistemática de la literatura con meta-análisis 1960-2014 / Validity of three methods for inmuno-diagnostic of neurocysticercosis: systematic review of the literature with meta-analysis 1960-2014

Introduction: The screening of neurocysticercosis is complex and immunological methods have varying validity. Objective: To evaluate the validity of ELISA for antigen and antibody, and EITB for antibody in the screening of neurocysticercosis. Methods: Meta-analysis of diagnostic tests with an ex-ante protocol implemented in five databases with 15 search strategies, ensuring reproducibility in the selection and extraction of information. Sensitivity, specificity, likelihood ratios (LR), diagnostic odds ratio and ROC curve were estimated in MetaDiSc, and predictive values, and Youden index were estimated in Epidat. Results: EITB presented sensitivity of 85.7% (95% CI 83.5-87.7), specificity 93.9% (95% CI = 92.7-95.0), PLR 19.6 (95% CI = 8,6-44.6), NLR 0.16 (95% CI = 0.12-0.21), OR diagnostic 136.2 (95% CI = 54.7-342.6) and area under the curve 0.926. In ELISA for antibody sensitivity was 87.5% (95% CI = 86.1-88.8), specificity 92.2% (95% CI = 91.4-93.0), PLR 11.3 (95% CI = 8.45-15.11), NLR 0.15 (95% CI = 0.13-0.18), diagnostic OR 87.4 (95% CI = 60.1-127.1) and area under the curve 0.950. ELISA for antigen showed low diagnostic validity. No differences were found in these parameters by sample, antigen or antibody type. Conclusion: ELISA for antibodies and EITB have a similar diagnostic value, detection of serum and CSF showed a similar validity.

Introducción: La tamización de neurocisticercosis es compleja y los métodos inmunológicos presentan validez variable y generalmente bajos tamaños de muestra. Objetivo: Evaluar la validez de ELISA para detección de antígeno y anticuerpo, y EITB para detección de anticuerpo en la tamización de neurocisticercosis. Métodos: Meta-análisis de pruebas diagnósticas con un protocolo ex-ante aplicado en cinco bases de datos con 15 estrategias de búsqueda, garantizando reproducibilidad en la selección y extracción de la información. Se estimó sensibilidad, especificidad, cocientes de probabilidad (CP), razón de odds diagnósticas y curva ROC en MetaDiSC, y valores predictores, índice de Youden y exactitud en Epidat. Resultados: EITB presentó sensibilidad de 85,7% (IC 95% = 83,5-87,7), especificidad 93,9% (IC9 5% = 92,7-95,0), CPP 19,6 (IC 95% = 8,6-44,6), CPN 0,16 (IC 95% = 0,12-0,21), OR diagnóstica 136,2 (IC 95% = 54,7-342,6) y área bajo la curva 0,926. En ELISA para anticuerpos la sensibilidad fue 87,5% (IC 95% = 86,1-88,8), especificidad 92,2% (IC 95% = 91,4-93,0), CPP 11,3 (IC 95% = 8,45-15,11), CPN 0,15 (IC 95% = 0,13-0,18), OR diagnóstica 87,4 (IC 95% = 60,1-127,1) y área bajo la curva 0,950. ELISA para antígeno presentó baja validez diagnóstica. No se hallaron diferencias en estos parámetros según tipo de muestra, antígeno o anticuerpo. Conclusión: ELISA para anticuerpos y EITB presentan una utilidad diagnóstica similar, la detección de suero presentó una validez similar al líquido cefalorraquídeo.

Neurocysticercosis, familial cerebral cavernomas and intracranial calcifications: differential diagnosis for adequate management / Neurocisticose, cavernoma cerebral familiar e calcificações intracranianas: diagnóstico diferencial e acompanhamento adequado

ABSTRACT Neurocysticercosis (NCC) is an endemic disease and important public health problem in some areas of the World and epilepsy is the most common neurological manifestation. Multiple intracranial lesions, commonly calcified, are seen on cranial computed tomography (CT) in the chronic phase of the disease and considered one of the diagnostic criteria of the diagnosis. Magnetic resonance imaging (MRI) is the test that better depicts the different stages of the intracranial cysts but does not show clearly calcified lesions. Cerebral cavernous malformations (CCM), also known as cerebral cavernomas, are frequent vascular malformations of the brain, better demonstrated by MRI and have also epilepsy as the main form of clinical presentation. When occurring in the familial form, cerebral cavernomas typically present with multiple lesions throughout the brain and, very often, with foci of calcifications in the lesions when submitted to the CT imaging. In the countries, and geographic areas, where NCC is established as an endemic health problem and neuroimaging screening is done by CT scan, it will be important to consider the differential diagnosis between the two diseases due to the differences in adequate management.

RESUMO A neurocisticercose (NCC) é um importante problema endêmico de saúde pública em algumas áreas do mundo, sendo epilepsia sua manifestação clínica mais comum. Múltiplas lesões intracranianas, geralmente com calcificações visualizadas em tomografia computorizada de crânio, são interpretadas como um dos critérios diagnósticos na fase crônica da doença. A ressonância magnética é o melhor teste de imagem para identificar a doença em diferentes estágios de sua forma cística mas apresenta limitações para demonstrar lesões calcificadas. Malformações cavernosas cerebrais, ou cavernomas, são malformações vasculares comuns ao sistema nervoso e epilepsia é também a sua forma mais frequente de apresentação. Na sua forma familiar cavernomas apresentam-se tipicamente com múltiplas lesões encefálicas e, frequentemente, com focos de calcificações na TC. Em alguns países, e determinadas regiões geográficas, onde neurocisticercose é endêmica, a neuroimagem mais usada para diagnóstico é a TC de crânio. Nesse contexto torna-se importante estabelecer bases para o diagnóstico diferencial entre as duas doenças, devido às diferentes formas de acompanhamento e tratamento adequado.

Analysis of cerebrospinal fluid in racemose form of neurocysticercosis / Análise do líquido cefalorraquidiano na forma racemosa da neurocisticercose

The present work aimed to evaluate the pattern of CSF alterations in patients diagnosed with neurocysticercosis (NCC) in racemose form.Method This is a retrospective cohort study of patients with diagnosis of NCC in racemose form. CSF samples from 26 patients were analyzed. After patient-chart analysis was performed descriptive analysis of case studies and comparison between sexes in relation to variables were obtained with CSF by Mann-Whitney and Student’s t-tests.Results The sexes did not differ statistically when compared to pleocytosis in CSF. Eosinophils were present in 31% in samples while the ELISA test presented 80% sensitivity in this case series. Of the patient total, 24 presented a meningitis pattern with lymphocytic predominance.Conclusion There was no difference in inflammatory pattern between the sexes, with predominance of lymphocytic meningitis and 80% sensitivity by ELISA test of CSF patients with racemose form of NCC.

O objetivo deste trabalho foi avaliar o padrão de alterações do LCR de pacientes com diagnóstico de neurocisticercose (NCC) na forma racemosa.Método Trata-se de estudo de coorte retrospectiva, de pacientes com diagnóstico de forma racemosa da NCC. Foram analisadas amostras de LCR de 26 pacientes. Após análise de prontuário foi realizada análise descritiva da casuística e comparação entre sexos em relação às variáveis obtidas com o LCR por meio dos testes de Mann-Whitney e t-Student.Resultados Não houve diferença estatisticamente significante quando comparado à pleocitose no LCR entre os sexos. Houve presença de eosinofilorraquia em 31% das amostras e o teste ELISA apresentou sensibilidade de 80% nesta casuística. Do total de paciente, 24 apresentaram padrão de meningite com predomínio linfocítico.Conclusão Não houve diferença no padrão inflamatório entre os sexos, com predomínio de meningite linfocítica e sensibilidade de 80% ao teste ELISA do LCR de pacientes da forma racemosa de NCC.

Afasia Paroxismal: epilepsia focal por cisticercosis cerebral, reporte de un caso / Paroxysmal Aphasia: focal epilepsy due to cerebral cysticercosis, a case report

Se reporta el caso de un paciente varón de 63 años; natural y procedente de Juliaca, que ingresó por un cuadro de episodios paroxismales de afasia transitoria, de 2 minutos de duración asociado a cefalea, sin trastorno de conciencia. No antecedentes de epilepsia, ni otros antecedentes patológicos. Al examen físico se evidenció episodios de parafasias semánticas y literales transitorias, de 1-2 minutos de duración. Los hallazgos de la tomografía cerebral y de la resonancia de encéfalo mostraron imágenes quísticas confluentes en valle silviano izquierdo de aspecto racemoso además de quistes vesiculares intraparenquimales peri-silvianos; los cuales resultaron definitivos para el diagnóstico. El presente caso de neurocisticercosis Mixta se manifestó como crisis epilépticas focales caracterizadas por afasia paroxismal, destacándose la presentación atípica. Se hace una breve revisión de la literatura...

We report a case of a 63-year old male patient; living in Juliaca, who was admitted with symptoms of paroxysmal episodes of transient aphasia lasting 2 minutes of associated with headache but without consciousness disturbances. He did not have history of epilepsy or other past medical history. Physical examination revealed transient semantic and literal paraphasias of 1 to 2 minutes of duration. The findings on computerized tomography (CT) and magnetic resonance imaging (MRI) of the brain disclosed multiple confluent cysts in clusters in the left sylvian fissure and vesicular perisylvian intraparenchymal cysts; all of which were definitive for the diagnosis. Highlighting the atypical presentation, this case of mixed neurocysticercosis was manifested as focal seizures characterized by paroxysmal aphasia. A brief literature review is presented...

Aspiración estereotáctica de una larva de Spirometra spp. / Stereotactic aspiration of Spirometra mansonides larvae

Brain sparganosis is a non-common parasite infection by Diphyllobothrium or Spirometra mansonoides larvae. This last one is responsible for most of the infestations in humans. We report a 19 years male patient bearer of a brain sparganosis. The patient presented with headache and left hemiparesis. CT diagnosis of right thalamic lesions was made and aspiration biopsy was performed using stereotactic system, obtaining a whole and death larvae. Histopathology confirms a CNS parasitism and it was treated initially with albendazol. ELISA test confirmed Spirometra spp. infestation. The patient developed asymptomatic with total remission of the lesions. It constitutes the second report in Cuba of brain sparganosis.

Se presenta el caso clínico de un varón con 19 años de edad y el diagnóstico de una esparganosis cerebral. Consultó por cefalea y una hemiparesia izquierda. En una tomografía computarizada cerebral con contraste se observaron lesiones talámicas derechas. Se realizó una biopsia cerebral guiada por estereotaxia con aspiración completa de un verme. En el estudio histopatológico se planteó un probable parasitismo de SNC y fue tratado inicialmente con albendazol. Se confirmó la infección por Spirometra spp. por test de ELISA. Evolucionó con regresión de síntomas y remisión imagenológica de las lesiones. Este caso constituye el segundo reporte en Cuba de una infestación cerebral por este parásito y aspiración estereotáctica de la larva de Spirometra spp.

Neurocysticercoiis in children presenting with febrile seizure: clinical profiile, imaging and serodiagnosis / Neurocisticercose em crianças apresentando crises afebris: perfil clínico, imagem e sorodiagnóstico

Neurocysticercosis (NCC) is one of the major causes of childhood seizures in developing countries including India and Latin America. In this study neurological pediatric cases presenting with afebrile seizures were screened for anti-Cysticercus antibodies (IgG) in their sera in order to estimate the possible burden of cysticercal etiology. The study included a total of 61 pediatric afebrile seizure subjects (aged one to 15 years old); there was a male predominance. All the sera were tested using a pre-evaluated commercially procured IgG-ELISA kit (UB-Magiwell Cysticercosis Kit ™). Anti-Cysticercus antibody in serum was positive in 23 of 61 (37.7%) cases. The majority of cases with a positive ELISA test presented with generalized seizure (52.17%), followed by complex partial seizure (26.08%), and simple partial seizure (21.73%). Headaches were the major complaint (73.91%). Other presentations were vomiting (47.82%), pallor (34.78%), altered sensorium (26.08%), and muscle weakness (13.04%). There was one hemiparesis case diagnosed to be NCC. In this study one child without any significant findings on imaging was also found to be positive by serology. There was a statistically significant association found between the cases with multiple lesions on the brain and the ELISA-positivity (p = 0.017). Overall positivity of the ELISA showed a potential cysticercal etiology. Hence, neurocysticercosis should be suspected in every child presenting with afebrile seizure especially with a radio-imaging supportive diagnosis in tropical developing countries or areas endemic for taeniasis/cysticercosis.

Neurocisticercose é uma das causas mais comuns de crises em crianças em países em desenvolvimento incluindo Índia e América Latina. Neste estudo casos neurológicos pediátricos, apresentando crises afebris foram selecionados através de anticorpos anti-Cysticercus (IgG) no seu soro para avaliar possível etiologia de Cysticercus. O estudo incluiu total de 61 casos pediátricos de indivíduos com crises afebris (idade de um a 15 anos); houve predominância de pacientes do sexo masculino. Todos os soros foram testados usando um kit comercial IgG-ELISA (UB-Magiwell Cysticercosis kit™) avaliado previamente. O anticorpo anti-Cysticercus no soro foi positivo em 23 de 61 casos (37,7%). A maioria dos casos com teste de ELISA positivo apresentava crises generalizadas (52,17%), seguida por casos de crises parciais complexas (26,08%) e crises parciais simples (21,73%). Dores de cabeça foram a queixa principal (73,91%). Outras manifestações foram vômitos (47,82%), palidez (34,78%), sensório alterado (26,08%) e fraqueza muscular (13,04%). Houve um caso de hemiparesia diagnosticado como NCC. Neste estudo uma criança sem quaisquer achados significantes às imagens apresentou sorologia positiva. Houve associação estatística significante entre os casos com múltiplas lesões no cérebro e a positividade pelo ELISA (p = 0,017). No seu conjunto a positividade pelo ELISA demonstra etiologia potencial para a cisticercose. Portanto neurocisticercose deve ser suspeitada em qualquer criança apresentado crises afebris com imagem que sugira diagnóstico em países tropicais em desenvolvimento ou em áreas endêmicas para teníase/cisticercose.

The relationship between neurocysticercosis and epilepsy: an endless debate / A relação entre neurocisticercose e epilepsia: um debate interminável

Neurocysticercosis (NC), or cerebral infection with Taenia solium, is an important public health problem worldwide. Among the neurological sequelae of NC, seizures have been described as the most common symptom. Acute symptomatic seizures often result from degeneration of a viable cyst; however, not all of these patients with acute or provoked seizures will develop epilepsy (i.e., recurrent unprovoked seizures). Because of the high prevalence of epilepsy and NC, a causal, as well as incidental relationship between the two may exist. The epileptogenicity of calcified cysts as well as the potential association between NC and hippocampal sclerosis necessitates future research. Antihelminthic treatment of NC results in disappearance of viable cysts in about one-third of patients with parenchymal disease, but a reduction in seizure recurrence has not been demonstrated in randomized controlled trials. Prevention is critical to reduce the burden of seizure and epilepsy related to NC.

A neurocisticercose (NC) ou infecção cerebral pela Taenia solium é importante problema de saúde pública em todo o mundo. Entre as sequelas neurológicas da NC, as crises convulsivas têm sido descritas como os sintomas mais frequentes. Crises convulsivas sintomáticas agudas resultam, muitas vezes, da degeneração de cistos viáveis; entretanto, nem todos os pacientes com NC e crises agudas ou provocadas desenvolvem epilepsia (i.e., crises recorrentes não provocadas). Pode haver uma relação entre epilepsia e NC, causal ou incidental, devido à alta prevalência de ambas. O potencial epileptogênico dos cistos calcificados assim como a possível associação entre NC e esclerose hipocampal ainda necessitam de futuras pesquisas. O tratamento anti-helmíntico da NC resulta no desaparecimento de cistos viáveis em cerca de 1/3 dos pacientes com a doença parenquimatosa, mas não foi demonstrada redução nas taxas de recorrência das crises convulsivas em estudos randomizados controlados. A prevenção é crítica para reduzir o contingente de crises convulsivas e epilepsia relacionadas à NC.

Pacientes con neurocisticercosis que no responden al tratamiento antiparasitario con albendazol en el Hospital Nacional L.N.S. - PNP durante Junio 2009 a Junio del 2011 / Patients with neurocysticercosis who do not respond to antiparasitic treatment with albendazole at the National Hospital LNS - PNP during June 2009 to June 2011

OBJETIVO: Determinar las características clínico-epidemiológicas de los pacientes con Neurocisticercosis que no responden al tratamiento antiparasitario con Albendazol en el Hospital Nacional Luis N. Sáenz-PNP durante Junio del 2009 a Junio del 2011. METODOLOGIA: Se realizó un estudio observacional, analítico-comparativo, retrospectivo, transversal. El tamaño de la población en estudio fue de 78 pacientes divididos en dos grupos: 33 pacientes con Neurocisticercosis que no responden al tratamiento antiparasitario con Albendazol y 45 pacientes con Neurocisticercosis que si responden al tratamiento antiparasitario con Albendazol. Las fuentes de información son las historias clínicas de aquellos pacientes con esta patología, que acudieron al Hospital Luis N. Sáenz durante Junio 2009 y Junio 2011. RESULTADOS: La edad promedio de los pacientes fue 37.7 años, con rangos de 18 a 34 años (41 por ciento), siendo la mayoría de sexo Masculino (65.4 por ciento). Las características sociodemográficas como la edad (p=0.973) y el sexo (p=0.243) no resultaron significativas con la respuesta o no al tratamiento antiparasitario con Albendazol. El 42.4 por ciento de los pacientes con NCC que no respondieron al tratamiento tuvieron un tiempo de enfermedad de 1 mes muy similar al 42.2 por ciento de los pacientes que si respondieron al tratamiento (p=0.344). El diagnóstico de la NCC en el 33.3 por ciento de los pacientes que no respondieron al tratamiento fue mediante Clínica y Neuroimágenes, a diferencia de los pacientes que si respondieron al tratamiento quienes tuvieron un diagnóstico mediante Clínica, Neuroimagen y Serología (26.7 por ciento) (p=0.129). Se observó que existe relación entre la localización de la NCC y la respuesta o no al tratamiento antiparasitario con Albendazol (p=0.002). La mayoría de los pacientes sin respuesta y con respuesta al tratamiento presentaron la forma quística (36.4 por ciento y 42.2 por ciento respectivamente) (p=0.832). Los principales signos y...

OBJECTIVE: To determine the clinical and epidemiological characteristics of the patients with neurocysticercosis that no responds to antiparasitic treatment with AIbendazol at National Hospital Luis N. Saenz-PNP during June 2009 to June 2011. METHODOLOGY: We conducted an observational study comparative-analytical, cross-sectional retrospective. The size of the study population was 78 patients divided into two groups: 33 patients with neurocysticercosis who do not respond to antiparasitic treatment with Albendazol and 45 patients with neurocysticercosis that whether they respond to antiparasitic treatment with AIbendazol. The sources of information are the clinical records of those patients with this pathology who attended the Hospital Luis N. Saenz during June 2009 and June 2011. RESULTS: The average age of the patients was 37.7 years oId, ranging from 18-34 years (41 per cent), the majority of male sex (65.4 per cent). The sociodemographic characteristics such as age (p=0.973) and sex (p=0.243) were not statistically significant with the answer or not to the antiparasitic treatment with Albendazol. The 42.4 per cent of patients with NCC who did not respond treatment had a disease duration of one month very similar to the 42.2 per cent of patients who did respond to treatment (p=0.344). The diagnosis of NCC in 33.3 per cent of patients who did not respond to the treatment was by Clinical and Neuroimaging, unlike patients who responded to treatment whether they had a diagnosis by clinical, neuroimaging and serology (26.7 per cent) (p=0.129). It was observed that there is relationship between the location of the NCC and the response or not to the Albendazol antiparasitic treatment (p=0.002). The majority of the patients with and without response to the treatment presented the form cystic (36.4 per cent and 42.2 per cent respectively) (p=0.832). The main signs and symptoms of patients with and without antiparasitic treatment response were: Nausea and vomiting...

Spinal intramedullary cysticercosis: a case report and literature review / Cisticercose intramedular: relato de caso e revisão da literatura

Neurocysticercosis is an endemic infeccion in Brazil, but the intramedullary cases are rare, 1,2% to 5,8% of all cases. There are only fifty cases reported until January of 2011. Intramedullary neurocysticerosis is a treatable pathology but if misdiagnosed it could lead to irreversible damage. Twenty eight year old female patient, previously healthy, was admitted due to a fall. She had progressive walking difficulties and impaired sensation in both lower limbs two months before admission. Contrast MRI revealed a round intramedullary cystic lesion at T2 e T3. The patient underwent laminectomy from T2 to T3, and the spinal cord was found locally swollen near the exit root at this level. A mielotomy was performed where a round protrusion was seen near the root. Histological examination of the resected sample showed cysticercosis. After surgical excision she received albendazol and streoids. The patient?s neurological function postoperatively was unchanged. One week later, the motor power of her lower limbs were grade 4/5, and she could walk without special support. The function of anal sphincter and bladder regained without compromise. She was back to work. This reflects dramatically in an active portion of population since it affects mostly people between 20 to 45 years. So it still represents a challenge and this paper intend to show our experience and by that help future diagnostics.

A neurocisticercose é uma doença endêmica no Brasil, mas os casos de lesão intramedular são raros, representando 1,2% a 5,8% das neurocisticercoses. Há apenas 50 casos relatados até 2011 na literatura. É uma patologia potencialmente tratável, mas erro diagnóstico pode causar dano neurológico irreversível. Apresentamos um caso de paciente de 28 anos, previamente hígida, admitida após uma queda. Relatava fraqueza progressiva e déficit sensitivo em membros inferiores com dois meses de evolução. Ressonância magnética revelou lesão cística intramedular em T2-T3. A paciente foi submetida à laminectomia T2-T3, com mietomia e ressecção de lesão cística completa. Exame histológico revelou cisticercose. Realizaremos revisão da literatura com ênfase no diagnóstico e tratamento da neurocisticercose medular, que podem representar um desafio ao neurocirurgião.

Cisteínoproteasas Catepsinas L de Taenia solium: Rol biológico en la infección y potencial uso para el inmunodiagnóstico de la neurocisticercosis / Cathepsin L Cysteine Protease from Taenia solium: Its biological role in the infection and potential use for the immunodiagnosis of neurocysticercosis

Taenia solium es un helminto aplanado responsable de la teniosis y de la cisticercosis humana, siendo esta última producida por el consumo de huevos infectivos. Los cisticercos pueden desarrollarse en diferentes tejidos del hombre, frecuentemente en el sistema nervioso central causando la neurocisticercosis (NCC). Para el diagnóstico de la NCC se requiere de una adecuada interpretación de datos clínicos, resultados de neuroimagen y pruebas serológicas. Sin embargo, las pruebas serológicas podrían mejorarse con el desarrollo de antígenos candidatos capaces de incrementar su sensibilidad y especificidad. En los últimos años se han descrito una serie de proteínas de superficie y de secreción de T. solium esenciales para la interacción parásito-hospedero. Una de estas familias son las cisteínoproteasas catepsinas L, las cuales cumplen un rol preponderante para el desarrollo y supervivencia del parásito, participando en la invasión tisular, la evasión de la respuesta inmune, el desenquistamiento y enquistamiento del cisticerco. Son consideradas como antígenos potenciales para el inmunodiagnóstico de la neurocisticercosis.

Taenia solium is a plane helminth responsible for taeniasis and human cysticercosis, the latter being the result of the consumption of infective eggs. Cysticerci can develop in different human tissues, often in the central nervous system, causing neurocysticercosis (NCC). For the diagnosis of NCC, an adequate interpretation of clinical data, neuroimaging results and serological tests are required. However, serological tests could be improved by developing candidate antigens able to increase their sensibility and specificity. In the last years, a series of surface and secretory proteins of T. solium essential for the parasite-host interaction have been described. One of these families is cathepsin L cysteine proteases, which have a predominant role in the development and survival of the parasite. They take part in the tissue invasion, immune response evasion, excystation and encystment of cysticercus. They are considered potential antigens for the immunodiagnosis of neurocysticercosis.