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1.
Animals (Basel) ; 13(13)2023 Jun 24.
Article in English | MEDLINE | ID: mdl-37443898

ABSTRACT

In Chile, studies of parasites from the family Sarcocystidae (Apicomplexa) have mostly been related to domestic animals. We aimed to assess the presence of Sarcocystidae taxa in cricetid rodents from Central and Southern Chile. We studied 207 rodents, encompassing six species, from 13 localities. We isolated DNA from tissue samples, amplified the Sarcocystidae 18S rRNA gene with polymerase chain reaction, and performed phylogenetic analyses using maximum likelihood and Bayesian inferences. In addition, we examined blood smears and performed histological studies in organs from Sarcocystidae DNA-positive animals. Three specimens were DNA-positive and three genotypes were retrieved and named: Sarcocystis sp. P61, related to Sarcocystis strixi, was detected in two Abrothrix olivacea. Toxoplasmatinae gen. sp. P99 was retrieved from those same two specimens, and was related to Toxoplasma and other genera, although it branched independently. Besnoitia sp. R34 was detected in one Abrothrix hirta, and was clustered with congeneric species associated with rodents. No protozoa were found during microscopic studies; thus, it was not possible to confirm parasitic interactions rather than accidental encounters. However, the close relatedness of the retrieved genotypes to parasites of rodents supports the hypothesis of host-parasite associations. All three genotypes are suggested as potential new taxa, including a putative new genus.

2.
Rev. invest. clín ; 74(3): 121-130, May.-Jun. 2022. tab, graf
Article in English | LILACS-Express | LILACS | ID: biblio-1409570

ABSTRACT

ABSTRACT Guillain-Barré syndrome (GBS) is the most frequent cause of acute flaccid paralysis and if not diagnosed and treated timely, a significant cause of long-term disability. Incidence in Latin America ranges from 0.71 to 7.63 cases/100,000 person-years. Historically, GBS has been linked to infections (mainly gastrointestinal by Campylobacter jejuni) and vaccines (including those against severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2]); however, a trigger cannot be detected in most cases. Regarding SARS-CoV-2, epidemiological studies have found no association with its development. Acute motor axonal neuropathy is the most common electrophysiological variant in Mexico and Asian countries. Intravenous immunoglobulin or plasma exchanges are still the treatment cornerstones. Mortality in Mexico can be as high as 12%. Advances in understanding the drivers of nerve injury in GBS that may provide the basis for developing targeted therapies have been made during the past decade; despite them, accurate criteria for selecting patients requiring acute treatment, prognostic biomarkers, and novel therapies are still needed. The newly-developed vaccines against SARS-CoV-2 have raised concerns regarding the potential risk for developing GBS. In the midst of coronavirus disease 2019 and vaccination campaigns against SARS-CoV-2, this review discusses the epidemiology, clinical presentation, management, and outcomes of GBS in Mexico.

3.
Animals (Basel) ; 12(6)2022 Mar 08.
Article in English | MEDLINE | ID: mdl-35327078

ABSTRACT

Echinococcosis is a neglected zoonosis that uses dogs and sheep as its main hosts in Chile. The Eg95 vaccine against sheep infection has been included in some control programs. Here, we assess the efficacy of the vaccination program in the hyperendemic Alto Biobío commune after 3 years of execution. Fisher's test and generalized linear models were used in the assessment. The program tried to offer a first dose at 2 months of age, a booster 1 month later, and yearly vaccination. Given logistic difficulties, important delays in vaccination occurred, and most animals did not receive the first booster. Dog deworming was not included in the program. Likely due to the aforementioned factors, the overall frequency of infection was not lower, but the proportion of large (>5 mm) cysts and fertile cysts was smaller after the program. The frequency of infection and/or the number of cysts were lower when the age at first dose was younger and the first booster was administered 1 month after the first dose. The results suggest that vaccination affects both cyst development after the larvae reach the target organs, as well as the development of the protoscolex once the cysts start developing.

4.
Rev Invest Clin ; 74(3): 121-130, 2022 05 01.
Article in English | MEDLINE | ID: mdl-35345064

ABSTRACT

Guillain-Barré syndrome (GBS) is the most frequent cause of acute flaccid paralysis and if not diagnosed and treated timely, a significant cause of long-term disability. Incidence in Latin America ranges from 0.71 to 7.63 cases/100,000 person-years. Historically, GBS has been linked to infections (mainly gastrointestinal by Campylobacter jejuni) and vaccines (including those against severe acute respiratory syndrome coronavirus 2 [SARS-CoV-2]); however, a trigger cannot be detected in most cases. Regarding SARS-CoV-2, epidemiological studies have found no association with its development. Acute motor axonal neuropathy is the most common electrophysiological variant in Mexico and Asian countries. Intravenous immunoglobulin or plasma exchanges are still the treatment cornerstones. Mortality in Mexico can be as high as 12%. Avances in understanding the drivers of nerve injury in GBS that may provide the basis for developing targeted therapies have been made during the past decade; despite them, accurate criteria for selecting patients requiring acute treatment, prognostic biomarkers, and novel therapies are still needed. The newly-developed vaccines against SARS-CoV-2 have raised concerns regarding the potential risk for developing GBS. In the midst of coronavirus disease 2019 and vaccination campaigns against SARS-CoV-2, this review discusses the epidemiology, clinical presentation, management, and outcomes of GBS in Mexico.


Subject(s)
COVID-19 , Guillain-Barre Syndrome , Vaccines , COVID-19 Vaccines , Guillain-Barre Syndrome/epidemiology , Guillain-Barre Syndrome/etiology , Guillain-Barre Syndrome/therapy , Humans , Mexico/epidemiology , SARS-CoV-2
5.
Chin Clin Oncol ; 10(4): 44, 2021 Aug.
Article in English | MEDLINE | ID: mdl-32527113

ABSTRACT

Access to healthcare in Mexico is available to its population via publicly and privately funded institutions. The public sector, administered by both the local and federal government under the jurisdiction of the Department of Health, provides healthcare to the majority of the country's population. Privately funded institutions vary in size and scope of practice, ranging from small clinics focused on family practice, to large tertiary hospitals with capacity for treating patients with complex conditions and performing clinical research. The evaluation and treatment of patients with cancer in Mexico is also available through both sectors. In the country's capital, Mexico City, patients with glioblastoma are primarily treated at the National Institute of Neurology and Neurosurgery and the National Institute of Oncology. Epidemiological data is incomplete due to the lack of a national cancer registry. In the case of neoplasms of the central nervous system, the available information suggests that gliomas represent 33% of all intracranial tumors. The treatment of patients in Mexico diagnosed with glioblastoma has not been standardized owing to the lack of resources in some communities and the expense of antineoplastic agents. Current options range from a biopsy only to maximal safe resection followed by adjuvant treatment with radiation and chemotherapy. Currently, basic science and clinical research is being conducted in academic institutions associated with universities and in private hospitals. Studies include the evaluation of tumor biology, neuroimaging biomarkers and new treatment options such as the use of chloroquine.


Subject(s)
Brain Neoplasms , Glioblastoma , Glioma , Brain Neoplasms/epidemiology , Brain Neoplasms/therapy , Glioblastoma/epidemiology , Glioblastoma/therapy , Glioma/epidemiology , Glioma/therapy , Humans , Mexico/epidemiology
6.
PLoS One ; 15(11): e0242743, 2020.
Article in English | MEDLINE | ID: mdl-33232364

ABSTRACT

Gestational Diabetes Mellitus (GDM) is characterized by abnormal maternal D-glucose metabolism and altered insulin signaling. Dysregulation of thyroid hormones (TH) tri-iodethyronine (T3) and L-thyroxine (T4) Hormones had been associated with GDM, but the physiopathological meaning of these alterations is still unclear. Maternal TH cross the placenta through TH Transporters and their Deiodinases metabolize them to regulate fetal TH levels. Currently, the metabolism of TH in placentas with GDM is unknown, and there are no other studies that evaluate the fetal TH from pregnancies with GDM. Therefore, we evaluated the levels of maternal TH during pregnancy, and fetal TH at delivery, and the expression and activity of placental deiodinases from GDM pregnancies. Pregnant women were followed through pregnancy until delivery. We collected blood samples during 10-14, 24-28, and 36-40 weeks of gestation for measure Thyroid-stimulating hormone (TSH), Free T4 (FT4), Total T4 (TT4), and Total T3 (TT3) concentrations from Normal Glucose Tolerance (NGT) and GDM mothers. Moreover, we measure fetal TSH, FT4, TT4, and TT3 in total blood cord at the delivery. Also, we measured the placental expression of Deiodinases by RT-PCR, western-blotting, and immunohistochemistry. The activity of Deiodinases was estimated quantified rT3 and T3 using T4 as a substrate. Mothers with GDM showed higher levels of TT3 during all pregnancy, and an increased in TSH during second and third trimester, while lower concentrations of neonatal TT4, FT4, and TT3; and an increased TSH level in umbilical cord blood from GDM. Placentae from GDM mothers have a higher expression and activity of Deiodinase 3, but lower Deiodinase 2, than NGT mothers. In conclusion, GDM favors high levels of TT3 during all gestation in the mother, low levels in TT4, FT4 and TT3 at the delivery in neonates, and increases deiodinase 3, but reduce deiodinase 2 expression and activity in the placenta.


Subject(s)
Diabetes, Gestational/blood , Gene Expression Regulation, Enzymologic , Iodide Peroxidase/biosynthesis , Placenta/metabolism , Thyroxine/blood , Triiodothyronine/blood , Adult , Diabetes, Gestational/pathology , Female , Humans , Placenta/pathology , Pregnancy , Iodothyronine Deiodinase Type II
7.
Rev. bras. parasitol. vet ; 28(4): 582-591, Oct.-Dec. 2019. tab, graf
Article in English | LILACS | ID: biblio-1057976

ABSTRACT

Abstract This research aimed to determine the presence of paramphistomids in cattle slaughtered in a slaughterhouse of the Ñuble Region of Chile, to identify flukes and to analyze the frequency of these parasites in the Maule, Ñuble, and Biobío administrative regions of Chile. Between October of 2016 and April of 2017, rumens of 494 cattle were examined for flukes in the forestomachs. Worms were identified morphologically and, in addition, molecular analysis of the internal transcriber spacer region 2 of the fluke's DNA was done and phylogenetic analyses were performed with Bayesian inference in 14 worms. The frequency was analyzed by locality (low- or highlands) and age. The overall frequency was 11.24%. The district with the highest frequency of presentation was Chillán Viejo (30.8%). Districts in the lowlands had similar frequencies to those in the mountain lands (p=0.1). The frequency of flukes was significantly higher in adult animals than in young ones (p<0.01). We obtained a 460 bp-length fragment of DNA that was identical to the sequences previously identified as Paramphistomum cervi and Calicophoron microbothrioides, and performed morphological analyses confirmed that our samples belonged to C. microbothrioides. This is the first published study of C. microbothrioides in Chile.


Resumo Este trabalho teve como objetivo determinar a presença de paramphistomídeos em bovinos abatidos em um matadouro da Região do Ñuble do Chile, para identificar parasitas e analisar a frequência desses parasitos nas regiões administrativas de Maule, Ñuble e Biobío, no Chile. Entre outubro de 2016 e abril de 2017, rúmens de 494 bovinos foram examinados à procura de vermes no pré-estômago. Os vermes foram identificados morfologicamente e, além disso, a análise molecular da região interna do espaçador do transcritor 2 do DNA e análises filogenéticas foram realizadas com inferência bayesiana em 14 vermes. A frequência foi analisada pela altitude da localidade (baixa ou alta) e idade. A frequência geral foi de 11,24%. O distrito com as maiores frequências de parasitismo foi Chillán Viejo (30,8%). Os distritos das terras baixas tinham frequências semelhantes às encontradas nas terras das montanhas (p=0,17). A frequência foi significativamente maior em animais adultos do que em jovens (p<0.01). Obtivemos um fragmento de DNA de 460 pb que era idêntico às sequências anteriores identificadas como Paramphistomum cervi e Calicophoron microbothrioides, e realizamos análises morfológicas que permitiram confirmar que nossas amostras pertenciam a C. microbothrioides. Este é o primeiro estudo publicado sobre C. microbothrioides no Chile.


Subject(s)
Animals , Paramphistomatidae/genetics , Cattle/parasitology , DNA, Helminth/genetics , Paramphistomatidae/anatomy & histology , Paramphistomatidae/classification , Phylogeny , Chile , Abattoirs , Sequence Analysis, DNA
8.
Rev Bras Parasitol Vet ; 28(4): 582-591, 2019.
Article in English | MEDLINE | ID: mdl-31721927

ABSTRACT

This research aimed to determine the presence of paramphistomids in cattle slaughtered in a slaughterhouse of the Ñuble Region of Chile, to identify flukes and to analyze the frequency of these parasites in the Maule, Ñuble, and Biobío administrative regions of Chile. Between October of 2016 and April of 2017, rumens of 494 cattle were examined for flukes in the forestomachs. Worms were identified morphologically and, in addition, molecular analysis of the internal transcriber spacer region 2 of the fluke's DNA was done and phylogenetic analyses were performed with Bayesian inference in 14 worms. The frequency was analyzed by locality (low- or highlands) and age. The overall frequency was 11.24%. The district with the highest frequency of presentation was Chillán Viejo (30.8%). Districts in the lowlands had similar frequencies to those in the mountain lands (p=0.1). The frequency of flukes was significantly higher in adult animals than in young ones (p<0.01). We obtained a 460 bp-length fragment of DNA that was identical to the sequences previously identified as Paramphistomum cervi and Calicophoron microbothrioides, and performed morphological analyses confirmed that our samples belonged to C. microbothrioides. This is the first published study of C. microbothrioides in Chile.


Subject(s)
Cattle/parasitology , DNA, Helminth/genetics , Paramphistomatidae/genetics , Abattoirs , Animals , Chile , Paramphistomatidae/anatomy & histology , Paramphistomatidae/classification , Phylogeny , Sequence Analysis, DNA
9.
J Wildl Dis ; 55(1): 270-272, 2019 01.
Article in English | MEDLINE | ID: mdl-30040017

ABSTRACT

Myxomas are an uncommon neoplasm in vertebrates, and are found at a low frequency in birds, both wild and domestic. We report myxomas in two Kelp Gulls ( Larus dominicanus) in Chile, identifying tumors in specimens that were received for necropsy.


Subject(s)
Bird Diseases/pathology , Charadriiformes , Myxoma/veterinary , Animals , Bird Diseases/epidemiology , Chile , Soft Tissue Neoplasms/epidemiology , Soft Tissue Neoplasms/pathology , Soft Tissue Neoplasms/veterinary
10.
Case Rep Rheumatol ; 2018: 8398453, 2018.
Article in English | MEDLINE | ID: mdl-30327741

ABSTRACT

INTRODUCTION: Inflammatory myopathies are a rare group of diseases characterized by proximal weakness. Incidence ranges from 7.98/million/year and prevalence at 14/100,000. The utility of [18F] fluorodeoxyglucose (FDG) positron emission tomography (PET)/computed tomography (CT) scan is increasing for the complementary diagnosis of myopathies. CASE REPORT: An 84-year-old male was admitted with a history of difficulty rising from a chair and a fall. Laboratory results showed increased creatine kinase levels of more than 50 times the normal reference values. Electromyography (EMG) showed myopathic changes, and FDG-PET/CT scan showed increased FDG uptake in bilateral quadriceps. A biopsy was performed revealing lymphocytic predominant infiltrates and myonecrosis. Prednisone and intravenous immunoglobulin (IVIG) were administered with strength improvement. The patient was discharged for further follow-up. DISCUSSION: FDG-PET/CT in inflammatory diseases has proven useful as muscle fibers have increased FDG uptake. In some cases, FDG-PET/CT is also useful in determining associated neoplastic diseases.

11.
Clin Case Rep ; 6(4): 596-602, 2018 04.
Article in English | MEDLINE | ID: mdl-29636921

ABSTRACT

Involvement of the central nervous system in sarcoidosis is rare; neurosarcoidosis, although unusual, can present as leptomeningitis. The diagnosis is usually difficult because of the vague and broad symptomatology; therefore, a prompt diagnosis should be made, and adequate treatment should be administered to reduce morbidity and mortality.

12.
PLoS One ; 12(8): e0182509, 2017.
Article in English | MEDLINE | ID: mdl-28817576

ABSTRACT

Placentas from gestational diabetes mellitus (GDM) are often hypervascularized; however, participation of vascular endothelial growth factor (VEGF) and its receptors in this placental adaptation is unclear. We aimed to test whether changes in phosphorylation of tyrosine 951 or tyrosine 1175 (pY951 or pY1175) of the vascular endothelial growth factor receptor 2 (KDR) are associated with the proangiogenic state observed in placentas from GDM. We obtained placental samples from women with normal pregnancies (n = 24) or GDM (n = 18). We measured the relative expression of markers for endothelial cell number (CD31, CD34), VEGF, vascular endothelial growth factor receptor 1 (Flt-1), KDR, pY951 and pY1175 of KDR in placental homogenate. Immunohistochemistry of placental blood vessels were performed using CD34. Proliferation and migration of human umbilical vein endothelial cells (HUVEC) obtained from normal pregnancy and GDM were determined in absence or presence of conditioned medium (CM) harvested from GDM or normoglycemic HUVEC cultures. GDM was associated with more CD31 and CD34 protein compared to normal pregnancy. High number, but reduced area of placental blood vessels was found in GDM. Reduced Flt-1 levels (mRNA and protein) are associated with reduced KDR mRNA, but higher KDR protein levels in placentas from GDM. No significant changes in Y951-or Y1175-phosphorylation of KDR in placentas from GDM were found. GDM did not alter proliferation of HUVECs, but enhanced migration. Conditioned medium harvested from GDM HUVEC cultures enhanced KDR protein amount, tube formation capacity and cell migration in HUVEC isolated from normoglycemic pregnancies. The data indicate that GDM is associated with reduced expression of Flt-1 but high pro-migratory activation of KDR reflecting a proangiogenic state in GDM.


Subject(s)
Cell Movement , Diabetes, Gestational/metabolism , Vascular Endothelial Growth Factor Receptor-1/metabolism , Vascular Endothelial Growth Factor Receptor-2/metabolism , Adult , Antigens, CD34/genetics , Antigens, CD34/metabolism , Biomarkers/metabolism , Cells, Cultured , Diabetes, Gestational/diagnosis , Female , Human Umbilical Vein Endothelial Cells/metabolism , Human Umbilical Vein Endothelial Cells/physiology , Humans , Infant, Newborn , Male , Placenta/metabolism , Platelet Endothelial Cell Adhesion Molecule-1/genetics , Platelet Endothelial Cell Adhesion Molecule-1/metabolism , Pregnancy , Vascular Endothelial Growth Factor A/metabolism , Vascular Endothelial Growth Factor Receptor-1/genetics
13.
Rev Med Inst Mex Seguro Soc ; 55(3): 330-340, 2017.
Article in Spanish | MEDLINE | ID: mdl-28440987

ABSTRACT

Central nervous system (CNS) tumors constitute a heterogeneous group of neoplasms that share a considerable morbidity and mortality rate. Recent advances in the underlying oncogenic mechanisms of these tumors have led to new classification systems, which, in turn, allow for a better diagnostic approach and therapeutic planning. Most of these neoplasms occur sporadically and several risk factors have been found to be associated with their development, such as exposure to ionizing radiation or electromagnetic fields and the concomitant presence of conditions like diabetes, hypertension and Parkinson's disease. A relatively minor proportion of primary CNS tumors occur in the context of hereditary syndromes. The purpose of this review is to analyze the etiopathogenesis, clinical presentation, diagnosis and therapy of CNS tumors with particular emphasis in the putative risk factors mentioned above.


Los tumores del sistema nervioso central (SNC) constituyen un grupo heterogéneo de neoplasias que tienen en común una morbimortalidad considerable. Los avances recientes en los mecanismos oncogénicos responsables del desarrollo de estos tumores han dado lugar a nuevos sistemas de clasificación, los cuales, a su vez, permiten un mejor abordaje diagnóstico y una mejor planificación terapéutica. La mayoría de estos tumores ocurren en forma esporádica y son varios los factores de riesgo que se han asociado a su desarrollo, tales como la exposición a radiaciones ionizantes o a ondas electromagnéticas, y la presencia de enfermedades como la diabetes, la hipertensión arterial y la enfermedad de Parkinson. Una proporción menor de casos de tumores primarios del SNC es causada debido a síndromes hereditarios. El propósito de esta revisión es resumir de manera integral la etiopatogenia, la presentación clínica, el diagnóstico y el tratamiento de los tumores del SNC y analizar objetivamente el papel que juegan en su desarrollo los factores de riesgo anteriormente mencionados.


Subject(s)
Central Nervous System Neoplasms , Central Nervous System Neoplasms/classification , Central Nervous System Neoplasms/diagnosis , Central Nervous System Neoplasms/etiology , Central Nervous System Neoplasms/therapy , Combined Modality Therapy , Humans , Prognosis , Risk Factors
14.
J Med Imaging (Bellingham) ; 2(2): 024503, 2015 Apr.
Article in English | MEDLINE | ID: mdl-26158107

ABSTRACT

Magnetic resonance imaging is a technique for the diagnosis and classification of brain tumors. Discrete compactness is a morphological feature of two-dimensional and three-dimensional objects. This measure determines the compactness of a discretized object depending on the sum of the areas of the connected voxels and has been used for understanding the morphology of nonbrain tumors. We hypothesized that regarding brain tumors, we may improve the malignancy grade classification. We analyzed the values in 20 patients with different subtypes of primary brain tumors: astrocytoma, oligodendroglioma, and glioblastoma multiforme subdivided into the contrast-enhanced and the necrotic tumor regions. The preliminary results show an inverse relationship between the compactness value and the malignancy grade of gliomas. Astrocytomas exhibit a mean of [Formula: see text], whereas oligodendrogliomas exhibit a mean of [Formula: see text]. In contrast, the contrast-enhanced region of the glioblastoma presented a mean of [Formula: see text], and the necrotic region presented a mean of [Formula: see text]. However, the volume and area of the enclosing surface did not show a relationship with the malignancy grade of the gliomas. Discrete compactness appears to be a stable characteristic between primary brain tumors of different malignancy grades, because similar values were obtained from different patients with the same type of tumor.

15.
Gac Med Mex ; 151(3): 403-15, 2015.
Article in Spanish | MEDLINE | ID: mdl-26089278

ABSTRACT

Glioblastoma multiforme is one of the most aggressive central nervous system tumors and with worse prognosis. Until now,treatments have managed to significantly increase the survival of these patients, depending on age, cognitive status, and autonomy of the individuals themselves. Based on these parameters, both initial or recurrence treatments are performed, as well as monitoring of disease by imaging studies. When the patient enters the terminal phase and curative treatments are suspended, respect for the previous wishes of the patient and development and implementation of palliative therapies must be guaranteed.


Subject(s)
Glioblastoma/therapy , Palliative Care/methods , Patient Care Team/organization & administration , Glioblastoma/pathology , Humans , Mexico , Neoplasm Recurrence, Local , Survival Rate , Terminal Care/methods
16.
Rev. sanid. mil ; 55(6): 265-270, nov.-dic. 2001. ilus
Article in Spanish | LILACS | ID: lil-326870

ABSTRACT

Sesión clinicopatológica del 12 de mayo del 2001. Mujer de 58 años, con antecedentes de diabetes mellitus, hipertensión arterial, en el último año con depresión y abuso de alcohol posterior al fallecimiento de su esposo. Ingresó al hospital con hemiparesia izquierda y disartria de inicio repentino. El estudio de tomografía axial demostró hemorragia talámica derecha extendida a la región parahipocampal derecha y diseminación al sistema ventricular, con desplazamiento leve de la línea media a la izquierda, y evidencia de infartos lacunares pontinos antiguos. La paciente se hospitalizó en la unidad de cuidados intensivos y presentó deterioro progresivo de sus constantes hemodinámicas, así como de su condición neurológica. Evolucionó al estado de choque con edema pulmonar falleciendo finalmente. El estudio posmortem demostró la hemorragia cerebral y los infartos lacunares observados en la tomografía de cráneo, arteriosclerosis generalizada grado III-A con infarto cardiaco antiguo con hipertrofia del ventrículo izquierdo, trombos sépticos en la aurícula derecha, tromboembolia pulmonar como causa directa de la muerte, bronconeumonía y edema pulmonar, pielonefritis crónica, hígado graso secundario a alcoholismo, infiltración adiposa del páncreas, y un adenoma paratiroideo como hallazgo incidental. Se trata de un caso típico de complicaciones de enfermedades crónicas comunes


Subject(s)
Humans , Female , Middle Aged , Pulmonary Edema , Diabetes Mellitus , Dysarthria , Paralysis/etiology , Alcoholism , Acute Kidney Injury
18.
Rev. sanid. mil ; 54(2): 71-5, mar.-abr. 2000. tab, CD-ROM
Article in Spanish | LILACS | ID: lil-292160

ABSTRACT

Se trata de un estudio prospectivo que se realizó para determinar la utilidad del video-EEG en el diagnóstico diferencial entre epilepsia y otros desórdenes convulsivos en la infancia. Se estudiaron 21 pacientes que cubrieron los criterios de inclusión. El diagnóstico previo al procedimiento era de epilepsia en 15 casos (71.4 por ciento) y en otros 6 era de crisis paroxísticas no epilépticas.Con el estudio se confirmó que 17 casos realmente tenían epilepsia (80.9 por ciento) y que sólo 4 tenían crisis paroxísticas (19.1 por ciento). El tratamiento previo se continuó sin cambios en 10 de los 17 casos y se modificó en los otros 7. Se eliminó todo tratamiento en los 4 niños cuyo estudio fue negativo. La sensibilidad del estudio fue de un 80 por ciento. En 2 casos sirvió para determinar con precisión la ubicación del foco epileptógeno y se consideran eventualmente candidatos a cirugía. El estudio permitió cumplir con los lineamientos establecidos por la Liga Internacional Contra la Epilepsia.


Subject(s)
Humans , Male , Female , Audiovisual Aids , Seizures/diagnosis , Epilepsy/diagnosis , Diagnosis, Differential , Electroencephalography/methods , Diagnostic Techniques, Neurological/trends
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