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1.
Rev. colomb. reumatol ; 30(1)mar. 2023.
Artigo em Inglês | LILACS | ID: biblio-1536225

RESUMO

Introduction: Vitamin D and vitamin D receptor (VDR) polymorphisms are associated with autoimmune diseases including systemic lupus erythematosus (SLE). The aim of this study is to assess the genetic association between VDR polymorphisms: TaqI, ApaI, Bsml and FokI and SLE with serum levels of Vitamin D in the Colombian Caribbean population. Method: Case and control study. One hundred and thirty-three patients with SLE and 100 healthy individuals were included. VDR polymorphism were genotyped by RT-PCR and Taqman® probes. Allelic, genotypic and haplotype associations were estimated. Serum vitamin D concentrations were quantified by Elisa. Values of 30 to 100ng/ml were established as a normal reference range. P values <.05 were considered statistically significant. Results: A high prevalence of SLE was observed in women (94%) and was associated with a higher risk of SLE [OR: 10.8; 95% CI: 4.7-24.6] (p<.05). Moreover, higher risk of SLE was observed in individuals with FokI VDR [rs2228570] [OR: 1.58; 95% CI: 1.05-2.36] in allelic models. The ACCA Haplotype of TaqI/ApaI/Bsml/FokI polymorphisms was associated with higher risk of SLE [OR = 2.28, 95% CI = 1.12-4.66, psim <.01]. Vitamin D deficiency was evidenced in 11.3% of the patients. Conclusion: In this study, the VDR rs2228570 polymorphism and ACCA haplotype were associated with higher SLE risk in an adolescent population.


Introducción: La vitamina D y los polimorfismos en el receptor de vitamina D (VDR) se asocian con enfermedades autoinmunes, incluido el lupus eritematoso sistémico (LES). El objetivo de este estudio es analizar la asociación genética entre los polimorfismos de VDR (Taql, Apal, Bsml y Fokl) y la susceptibilidad al LES, así como su relación con los niveles séricos de vitamina D en población del Caribe colombiano. Metodología: Estudio de casos y controles. Se incluyeron 133 pacientes adultos con diagnóstico de LES y 100 individuos sanos. Los polimorfismos VDR fueron genotipados por RT-PCR y sondas Taqman®. Se estimaron asociaciones alélicas, genotípicas y haplotípicas. Las concentraciones séricas de vitamina D fueron cuantificadas por Elisa. Se establecieron valores de 30 a 100ng/ml como rango normal de referencia. Valores p<0,05 fueron considerados estadísticamente significativos. Resultados: Se observó una alta prevalencia de LES en pacientes femeninas (94%) y se asoció a mayor riesgo de LES (OR: 10,8; IC95%: 4,7-24,6; p < 0,05). Se evidenció mayor riesgo de LES en individuos con polimorfismo Fokl del gen VDR [rs2228570] (OR: 1,58; IC95%: 1,05-2,36) en modelos alélicos. El haplotipo ACCA de los polimorfismos Taql, Apal, Bsml y Fokl se asoció a mayor riesgo de LES (OR: 2,28, IC95%: 1,12-4,66; psim<0,01). Se evidenció deficiencia de vitamina D en el 11,3% de los pacientes. Conclusión: En este estudio, el polimorfismo VDR rs2228570 y el haplotipo ACCA se asociaron a mayor riesgo de LES en población adolescente.


Assuntos
Humanos , Feminino , Compostos Policíclicos , Polimorfismo Genético , Variação Genética , Vitamina D , Doenças da Pele e do Tecido Conjuntivo , Doenças do Tecido Conjuntivo , Fenômenos Genéticos , Compostos de Anéis Fundidos , Lúpus Eritematoso Sistêmico
2.
Infectio ; 26(1): 3-10, ene.-mar. 2022. graf
Artigo em Inglês | LILACS-Express | LILACS | ID: biblio-1350841

RESUMO

Abstract In recent months, rare cases of thrombosis at unusual sites associated with thrombocytopenia, occurring within a typical risk window (i.e., 4-28 days) after receiving SARS CoV2 vaccines, have been reported. Healthcare professionals should be prepared to detect these cases on time. The Expert Panel of the Knowledge Management and Transfer Network conducted a free search of the related literature. With the available information and the clinical expertise of the working group, we formulated, reviewed, and endorsed recommendations for the timely suspicion, diagnosis (case definitions, the use of initial laboratory and imaging tests, specific tests), and management of these thrombotic conditions. This document is considered a living document that will be updated as new evidence emerges, and recommendations may change over time.


Resumen En meses recientes se han reportado casos raros de trombocitopenia y trombosis en sitios inusuales, que ocurren dentro de una ventana de riesgo típica ( por ejemplo de 4 a 28 días) luego de recibir vacunas de SARS CoV 2. Los profesionales de la salud deben estar preparados para detectar estos casos a tiempo. Un panel de expertos y una red de transferencia de conocimiento realizó una búsqueda libre de literatura seleccionada. Con la información disponible y la experticia clínica del grupo de trabajo revisamos y dimos recomendaciones para la sospecha temprana, el diagnostico (definición de caso, el uso de pruebas de laboratorio especificas y de imágenes diagnósticas) para le manejo de estas condiciones tromboticas. Este documento es considerado un documento vivo que debe ser actualizado a medida que surja nueva evidencia y las recomendaciones vayan cambiando con el tiempo

3.
Rev. colomb. nefrol. (En línea) ; 8(1): e202, ene.-jun. 2021. tab, graf
Artigo em Espanhol | LILACS-Express | LILACS | ID: biblio-1347364

RESUMO

Resumen Introducción: la dieta con restricción de proteínas parece tener un papel importante en la progresión de la enfermedad renal crónica (ERC) y la aparición anticipada de síntomas urémicos, además la suplementación de aminoácidos esenciales ofrece aparente seguridad para lograr restricciones agresivas de proteínas. Objetivo: realizar una revisión de la literatura para establecer las recomendaciones de uso práctico sobre la dieta con restricción de proteínas en la ERC avanzada. Materiales y métodos: se realizó una búsqueda estructurada rápida de la literatura en la que se incluyeron revisiones sistemáticas y metaanálisis, de los cuales se extrajeron las respuestas de las preguntas con estructura PICOT diseñadas a priori. Los resultados fueron sometidos a consenso para generar recomendaciones prácticas. Resultados: se incluyeron 6 revisiones sistemáticas de la literatura con una evaluación de calidad moderada. Según los hallazgos, una dieta muy baja en proteínas con suplementación de alfa-cetoanálogos beneficia a los pacientes que ingresan a diálisis o son sometidos a trasplante renal, además reduce la progresión de la enfermedad. No obstante, se requiere de ensayos clínicos con mejor calidad que consideren aspectos como la calidad de vida. Conclusiones: aunque la evidencia es de baja calidad, se establece que la dieta muy baja en proteínas y suplementada con alfa-cetoanálogos en pacientes adecuadamente seleccionados reduce el deterioro de la tasa de filtración glomerular y parece reducir el ingreso a diálisis. Por tanto, se recomienda hacer un seguimiento estricto y periódico en el que se vigilen las medidas antropométricas y el perfil de riesgo de desnutrición.


Abstract Introduction and objective: The protein-restricted diet appears to play an important role in the progression of chronic kidney disease and the early onset of uremic symptoms, the supplementation of essential amino acids offers apparent security in achieving aggressive protein restrictions. The objective of this document is to carry out a literature review to inform practical use recommendations on this behavior in advanced Renal Disease (CKD). Materials and methods: A quick structured search of the literature is carried out, with the selection of systematic reviews and meta-analyzes, from which the answers to the questions with a PICOT structure designed a priori are extracted. The results were submitted to consensus to generate practical recommendations. Results: six systematic reviews of the literature were included, with a moderate quality evaluation, the extraction of the information reports an apparent benefit of the very low protein diet with supplementation of alpha-keto-analogues on admission to dialysis or kidney transplantation and a consistent reduction of disease progression. Better clinical trials that integrate outcomes such as quality of life are required. Conclusions: With low quality of evidence, the very low protein diet, supplemented with alpha-keto analogues, in the properly selected patient, reduces the deterioration of the glomerular filtration rate, seems to reduce admission to dialysis. Regular strict monitoring is recommended, with monitoring of anthropometric measures and malnutrition risk profile.

5.
Rev. colomb. nefrol. (En línea) ; 7(supl.2): 50-69, jul.-dic. 2020. tab
Artigo em Espanhol | LILACS, COLNAL | ID: biblio-1251579

RESUMO

resumen está disponible en el texto completo


Abstract Introduction: The numbers of SARS-CoV-2 infection in the pediatric population are low so far. There is limited information about the behavior of SARS-CoV-2 in a pediatric patient with chronic kidney disease. Objective: To formulate informed recommendations to the prevention, diagnosis, and management of SARS-CoV-2 infection in pediatric patients with kidney disease or acute kidney injury associated with COVID-19 in Colombia. Methodology: A rapid systematic review was performed in Embase and Pubmed databases and scientific societies, to answer questions prioritized by clinical experts in pediatric nephrology. The quality of the evidence was evaluated with validated tools according to the type of study. The preliminary recommendations were consulted by an expert group. The agreement was defined when approval was obtained from at least 70% of the experts consulted. Results: A response was obtained from ' 9 experts in pediatric nephrology in Colombia, who declared the conflict of interest before the consultation. The range of agreement for the recommendations ranged from 78.9% to '00%. The recommendations did not require a second consultation. Conclusion: The evidence-based recommendations for the management of a patient with kidney disease and COVID-19 in the Colombian context are presented.


Assuntos
Humanos , Masculino , Feminino , Pré-Escolar , Criança , Adolescente , Pediatria , COVID-19 , Pacientes , Sociedades Científicas , Colômbia , Insuficiência Renal Crônica , Injúria Renal Aguda , Nefrologia
6.
Rev. colomb. nefrol. (En línea) ; 7(supl.2): 89-117, jul.-dic. 2020. tab
Artigo em Espanhol | LILACS, COLNAL | ID: biblio-1251581

RESUMO

resumen está disponible en el texto completo


Abstract Introduction: Acute kidney injury is a frequent complication in patients with COVID-19 and its occurrence is a potential indicator of multi-organ dysfunction and disease severity. Objective: Develop, through an expert consensus, evidence-based recommendations for the prevention, diagnosis, and management of acute kidney injury in patients with SARS CoV2 / COVID-19 infection. Materials and methods: Based on a rapid systematic review in Embase and Pubmed databases and documents from scientific societies, we made preliminary recommendations and consulted with an expert group through an online tool. Then we defined agreement after at least 70 % consensus approval. Quality evidence was evaluated according to the type of document included. The strength of the recommendations was graded as strong or weak. Results: Fifty clinical experts declared their conflict of interest; the consultation took place between May 2 and 29, 2020. The range of agreement ranged from 75.5 % to 100 %. Recommendations for prevention, diagnosis and management of acute kidney injury in patients with SARS CoV2 infection are presented. Conclusions: Although the good quality information available regarding acute kidney injury in patients with COVID-19 is scarce, the recommendations of clinical experts will guide clinical decision-making and strategies around patients with this complication, guaranteeing care focused on the people, with high quality standards, and the generation of safety, health and wellness policies for multidisciplinary care teams.


Assuntos
Humanos , Masculino , Feminino , COVID-19 , Pacientes , Colômbia , Diagnóstico , Injúria Renal Aguda
7.
Rev. colomb. nefrol. (En línea) ; 7(supl.2): 119-159, jul.-dic. 2020. tab
Artigo em Espanhol | COLNAL, LILACS | ID: biblio-1251582

RESUMO

Resumen Introducción: Las personas con diálisis de mantenimiento se consideran una población en alto riesgo de infección por SARS-CoV-2, complicaciones y muerte. La periodicidad de la diálisis, la organización y la demanda en las unidades de diálisis y las limitaciones de alfabetización en salud poblacional limitan el cumplimiento del aislamiento y el distanciamiento social. Objetivo: Desarrollar, mediante un consenso de expertos, recomendaciones informadas en evidencia para la prevención, el diagnóstico y el manejo de la infección por SARS-CoV-2/COVID-19 en pacientes con enfermedad renal crónica. Materiales y métodos: Se realizó una revisión rápida de literatura en Pubmed, Embase y sociedades científicas. La calidad de evidencia fue evaluada según el tipo de estudio incluido. El acuerdo se definió para cada recomendación con umbral de al menos 70% de aprobación. La fuerza de las recomendaciones fue graduada como fuerte o débil. Resultados: El colectivo fue consultado entre el 17 y 19 de mayo de 2020. Se obtuvo respuesta de 44 expertos clínicos que declararon conflicto de interés previo a la consulta. El acuerdo de las recomendaciones estuvo entre 70,5 y 100%. Se presentan las recomendaciones de un colectivo experto para la prevención, el diagnóstico y el manejo de infección por SARS-CoV-2/COVID-19 en pacientes con enfermedad renal crónica. Conclusión: Debido a la reciente aparición de la infección por SARS-CoV-2 y las incertidumbres respecto a la prevención, el diagnóstico y el manejo, las recomendaciones presentadas se conciben como un estándar colombiano que permita garantizar un cuidado centrado en las personas con enfermedad renal crónica y la protección de los profesionales de la salud.


Abstract Introduction: People with chronic dialysis are considered a population at high risk of SARS CoV2 infection and its derived complications and death. The need to go to strict dialysis schedules, the high demand in the kidney facilities and the difficulties derived from the time and space organization in the rooms in the face to the pandemic added to the difficult learning, teaching and adapting new protocols manifest the needed of standard recommendation according to this problem in people who couldn't have an ideal isolation. Objective: Develop through an expert consensus, evidence-informed recommendations for the prevention, diagnosis, and management of SARS-CoV-2/COVID-19 infection in patients with chronic kidney disease on Dialysis. Materials and methods: We carried out a quick literature review, PubMed, Embase and scientific societies were consulted. The quality of the evidence was considered according to the type of study included. The agreement threshold defined for each recommendation was > 70% approval among experts. The strength of the recommendations was rated as strong or weak. Results: Between May 17 and 19, 2020, was conformed a team of 44 clinical experts who declared their interest conflict prior to the consultation. The agreement of the recommendations was between 70.5% and 100%. The recommendations were separated in prevention, early identification, and diagnostic, isolation in hemodialysis facilities and peritoneal dialysis, and team protection. Ethical considerations also were included. Conclusion: Due to the recent appearance of SARS-CoV-2 infection and the uncertainties regarding prevention, diagnosis and management, the recommendations presented are conceived as a Colombian standard that allows guaranteeing focused care for people with chronic kidney disease and the protection of health team.


Assuntos
Humanos , Masculino , Feminino , Insuficiência Renal Crônica , COVID-19 , Pacientes , Diálise Renal , Colômbia , Diagnóstico
8.
Biomédica (Bogotá) ; 40(supl.2): 50-67, oct. 2020. tab, graf
Artigo em Espanhol | LILACS | ID: biblio-1142448

RESUMO

A finales del 2019 se inició en Wuhan, China, el brote de un nuevo coronavirus que se dispersó por todo el mundo infectando y cobrando miles de vidas. Se ha encontrado que ciertas comorbilidades constituyen factores de riesgo para resultados poco satisfactorios de la enfermedad, pero es poco lo que se ha descrito sobre pacientes en hemodiálisis, a pesar de tratarse de una población de alto riesgo de infección, complicaciones y muerte. En este artículo se describe el curso clínico, las manifestaciones clínicas y las complicaciones de la COVID-19 en siete pacientes en hemodiálisis permanente y se hacen recomendaciones para el manejo de pacientes con enfermedad renal crónica.


At the end of 2019, in Wuhan, China, the outbreak of a new coronavirus began and quickly spread throughout the world infecting and claiming thousands of lives. To date, certain comorbidities are known to be risk factors for unsatisfactory disease outcomes, but little has been reported regarding hemodialysis patients despite being a population at high risk of infection, complications, and death. Here we describe the clinical course, clinical manifestations and complications of COVID-19 in seven patients on permanent hemodialysis. We also make recommendations for the management of patients with chronic kidney disease.


Assuntos
Diálise Renal , Infecções por Coronavirus , Relatos de Casos , Síndrome Respiratória Aguda Grave
9.
Herrera-Molina, Emilio; González, Nancy Yomayusa; Low-Padilla, Eduardo; Oliveros-Velásquez, Juan David; Mendivelso-Duarte, Fredy; Gómez-Gómez, Olga Victoria; Castillo, Ana María; Barrero-Garzón, Liliana Isabel; Álvarez-Moreno, Carlos Arturo; Moscoso-Martínez, Ernesto Augusto; Ruíz-Blanco, Pilar Cristin; Luna-Ríos, Joaquín Gustavo; Ortiz, Natasha; Herrera, Emiliano Mauricio; Guevara-Santamaría, Fabián; Moreno-Gómez, Jairo Enrique; Cárdenas-Ramírez, Héctor Mauricio; González-González, Camilo Alberto; Jannauth, María José; Patiño-Pérez, Adulkarin; Pinto, Diego Alejandro; Acevedo, Juan Ramon; Torres, Rodolfo Eduardo; Montero, Jairo Camilo; Acevedo, Andrés David; Caceres, Ximena Adriana; Acuña-Olmos, Jairo; Arias, Carlos Andrés; Medardo-Rozo, José; Castellanos-Parada, Jeffrey; López-Miranda, Ángelo Mauricio; Pinzón-Serrano, Estefanía; Rincón-Sierra, Oswaldo; Isaza-Ruget, Mario; Suárez-Ramos, María del Pilar; Vargas-Rodríguez, Johanna; Mejia-Gaviria, Natalia; Moreno-Marín, Sandra Yadira; García-Guarín, Bibiana María; Cárdenas, Martha Lucía; Chavarro, Luis Fernando; Ronderos-Bernal, Camila; Rico-Landazabal, Arturo; Coronado-Daza, Jorge Antonio; Alfaro-Tejeda, Mercedes Teresa; Yama-Mosquera, Erica; Hernández-Sierra, Astrid Patricia; Restrepo-Valencia, César Augusto; Arango-Álvarez, Javier; Rosero-Olarte, Francisco Oscar Fernando; Medina-Orjuela, Adriana; Robayo-García, Adriana; Carballo-Zarate, Virgil; Rodríguez-Sánchez, Martha Patricia; Bernal, Dora P.; Jaramillo, Laura; Baquero-Rodríguez, Richard; Mejía-Gaviria, Natalia; Aroca, Gustavo.
Artigo em Espanhol | LILACS-Express | LILACS | ID: biblio-1535986

RESUMO

está disponible en el texto completo


The exponential increase in the request for laboratory tests of 25-Hydroxyvitamin D or [25 (OH) D has ignited the alarms and generated a strong call for attention, since it may reflect deficiencies in the standardization of clinical practice and in the use non-systematic scientific evidence for decision-making in real life, which allows to analyze the indications of the test, its frequency, interpretation and even to assess the impact for health systems, especially when contrasted with the minimum or almost. No effects of the strategy of screening or supplying indiscriminately to the general population, without considering a comprehensive clinical assessment of risks and needs of people. From a purely public health impact point of view, the consequence of massive and unspecified requests is affecting most of the health systems and institutions at the global level. The primary studies that determined average population intake values have been widely used in the formulation of recommendations in Clinical Practice Guidelines, but unfortunately misinterpreted as cut points to diagnose disease and allow the exaggerated prescription of nutritional substitution. The coefficient of variation in routine tests to measure blood levels of 25 (OH) D is high (28%), decreasing the overall accuracy of the test and simultaneously, increasing both the falsely high and falsely low values. The most recent scientific evidence analyzes and seriously questions the usefulness and the real effect of the massive and indiscriminate practice of prescribing vitamin D without an exhaustive risk analysis. The available evidence is insufficient to recommend a general substitution of vitamin D to prevent fractures, falls, changes in bone mineral density, incidence of cardiovascular diseases, cerebrovascular disease, neoplasms and also to modify the growth curve of mothers' children. They received vitamin D as a substitute during pregnancy. The recommendations presented in the document are based on the critical analysis of current evidence and the principles of good clinical practice and invite to consider a rational use of 25 (OH) D tests in the context of a clinical practice focused on people and a comprehensive assessment of needs and risks. The principles of good practice suggest that clinicians may be able to justify that the results of the 25 (OH) D test strongly influence and define clinical practice and modify the outcomes that interest people and impact their health and wellness. Currently there is no clarity on how to interpret the results, and the relationship between symptoms and 25 (OH) D levels, which may not be consistent with the high prevalence of vitamin D deficiency reported. For this reason, it is suggested to review the rationale of the request for tests for systematic monitoring of levels of 25 (OH) D or in all cases where substitution is performed. Consider the use of 25 (OH) D tests within the comprehensive evaluation of people with suspicion or confirmation of the following conditions: rickets, osteomalacia, osteoporosis, hyper or hypoparathyroidism, malabsorption syndromes, sarcopenia, metabolic bone disease.

10.
Biomédica (Bogotá) ; 37(2): 260-266, abr.-jun. 2017. tab, graf
Artigo em Espanhol | LILACS | ID: biblio-1038787

RESUMO

RESUMEN Introducción. El lupus eritematoso sistémico es una enfermedad autoinmunitaria cuya gravedad varía según la raza, el sexo y la edad de aparición. Esta disparidad también se observa en los marcadores genéticos asociados con la enfermedad presentes en los genes PTPN22, VDR y TNF. La estratificación genética que presentan las diferentes poblaciones en el mundo puede influir en dicha variabilidad. Objetivo. Analizar la asociación de variantes genéticas de los genes PTPN22, VDR y TNF con nefritis lúpica en niños y su caracter de hereditarias en familias colombianas. Materiales y métodos. Se llevó a cabo un estudio basado en familias con 46 tríos (caso, padre y madre). Se hizo la genotipificación de las variantes rs2476601 de PTPN22, rs361525 y rs1800629 del TNF, y TaqI [rs731236], ApaI [rs7975232], BsmI [rs1544410] y FokI [rs2228570] del VDR, mediante reacción en cadena de la polimerasa cuantitativa (quantitative Polymerase Chain Reaction, qPCR). Se estimó el efecto de la transmisión del alelo de riesgo de padres a hijos y el desequilibrio de ligamiento de los loci VDR y TNF. Resultados. Se observó que el alelo A de rs2476601 en PTPN22 se distribuyó en 8,69 % (n=16) de los padres y en 19,5 % (n=18) de los casos, y que su transmisión de padres a hijos fue 17 veces mayor con relación al alelo G (p=0,028). Los polimorfismos de TNF y VDR no presentaron desequilibrio de transmisión. Las variantes TaqI, ApaI y BsmI del VDR presentaron desequilibrio de ligamiento. Conclusión. Estos hallazgos evidenciaron una asociación del polimorfismo rs2476601 de PTPN22 con la nefritis lúpica en niños, determinada por su transmisión en el grupo de familias estudiadas.


ABSTRACT Introduction: Systemic lupus erythematosus is an autoimmune disease in which the severity varies according to race, sex and age of onset. This variation is also observed in the genetic markers associated with the disease, including PTPN22, VDR and TNF genes. The genetic stratification in different populations worldwide can influence the variability. Objective: To analyze the heritability of PTPN22, VDR and TNF genetic variants and their association with pediatric lupus nephritis in Colombian families. Materials and methods: We conducted a family-based study including 46 triads (case, father and mother). The variants rs2476601 of PTPN22; rs361525 and rs1800629 of TNF, and TaqI [rs731236], ApaI [rs7975232], BsmI [rs1544410] and FokI [rs2228570] of VDR were genotyped by qPCR. The effects of overtransmission of the risk allele from parents to children and linkage disequilibrium at the VDR and TNF loci were estimated. Results: We found that allele A of rs2476601 in PTPN22 was distributed among 8.69 % (n=16) of the parents and 19.5 % (n=18) of the cases; this allele was overtransmitted from parents to children 17 times more often than the G allele (p=0.028). TNF and VDR polymorphisms did not exhibit transmission disequilibrium. VDR TaqI, ApaI and BsmI variants exhibited linkage disequilibrium. Conclusion: These findings showed an association between the PTPN22 rs2476601 polymorphism and pediatric lupus nephritis due to its overtransmission in the group of families studied.


Assuntos
Criança , Humanos , Nefrite Lúpica/complicações , Fator de Necrose Tumoral alfa/genética , Receptores de Calcitriol/genética , Polimorfismo de Nucleotídeo Único/genética , Proteína Tirosina Fosfatase não Receptora Tipo 22/genética , Lúpus Eritematoso Sistêmico/complicações , Nefrite Lúpica/genética , Fator de Necrose Tumoral alfa/química , Receptores de Calcitriol/metabolismo , Receptores de Calcitriol/química , Colômbia , Polimorfismo de Nucleotídeo Único/fisiologia , Alelos , Proteína Tirosina Fosfatase não Receptora Tipo 22/metabolismo , Proteína Tirosina Fosfatase não Receptora Tipo 22/química , Genótipo , Lúpus Eritematoso Sistêmico/genética
11.
Salud UNINORTE ; 31(2): 358-366, mayo-ago. 2015. ilus, tab
Artigo em Espanhol | LILACS-Express | LILACS | ID: lil-769275

RESUMO

El uso recreacional de drogas psicoactivas es una práctica generalizada en población de adultos jóvenes en el mundo. Existe evidencia de que los opioides y la cocaína producen toxicidad renal. La necrosis tubular aguda, rabdomiolisis y la glomerulonefritis focal segmentaria son las presentaciones más comunes. Reportamos un caso de daño renal agudo en un joven después del uso recreacional de alcohol, cocaína y opioides, cuyos hallazgos patológicos son descritos brevemente en la literatura.


Recreational drug use is a widespread activity in the young adult population. Cocaine and opioids have well described mechanism for renal toxicity, they include local and systemic toxicity, acute tubular necrosis, rhabdomylolysis and focal segmental glomerulosclerosis are among the most common presentations. We report a case of acute kidney injury in a young man after the recreational use of alcohol, cocaine and opioids, the pathological findings are described and a brief review of the literature is presented.

12.
Rev. colomb. obstet. ginecol ; 62(3): 261-266, jul.-sept. 2011. ilus
Artigo em Espanhol | LILACS | ID: lil-603952

RESUMO

Introducción: el carcinoma metaplásico de la mama tipo células escamosas es una neoplasia maligna poco frecuente que representa un 0,04% de los carcinomas mamarios. Su diagnóstico clínico e imagenológico es complejo dado la similitud con lesiones benignas; sin embargo, su rápido crecimiento alerta sobre su comportamiento agresivo. Debido a los pocos casos en la literatura, no hay un consenso general sobre su diagnóstico y tratamiento. Se presenta un caso con el objetivo de hacer una revisión sobre el tema respecto al diagnóstico histopatológico y factores pronósticos. Caso clínico: se presenta el caso clínico de una paciente de 51 años, con una de masa de 6 cm en mama derecha, cuyos estudios ecográficos reportaron una probable lesión benigna (Breast Imaging Reporting and Data System - BIRADS III). El estudio histopatológico revela una lesión tumoral maligna constituida por células escamosas que tapizan espacios quísticos. Materiales y métodos: para la revisión de la literatura se exploró la base de datos PubMed, con el fin de buscar revisiones sistemáticas, presentación de casos clínicos, estudios clínicos y epidemiológicos con las palabras clave metaplastic breast carcinoma, metaplastic carcinoma, durante el período comprendido entre el 2000-2011. Conclusiones: histopatológicamente, el carcinoma metaplásico de células escamosas puede presentarse como una mezcla de adenocarcinoma con áreas dominantes de diferenciación escamosa, e incluso, en formas escamosas puras, representando plasticidad fenotípica del tumor. El sistema modificado de Scarf-Bloom-Richardson no es aplicable en esta lesión. Los factores pronósticos más importantes son la edad y el tamaño tumoral; sin embargo, algunos estudios consideran las metástasis nodales y el estado de los receptores.


Introduction: squamous cell-type metaplastic breast carcinoma is an unusual malign neoplasia, accounting for 0.04% of breast carcinomas. Its clinical and imagenologic diagnosis is complex, given its similarity with benign lesions; however, its rapid growth alerts doctors concerning its aggressive behavior. No general consensus was found about its diagnosis and treatment due to the few pertinent cases published to date in the literature. A case is presented, aimed at reviewing the topic regarding histopathological diagnosis and prognostic factors. Clinical case: a clinical case of a 51 year-old patient is presented; she had a 6 cm mass in her right breast and ecographic studies (Breast Imaging Reporting and Data System - BIRADS III) reported a probable benign lesion. The histopathological study revealed a malignant tumor consisting of squamous cells lining cystic spaces. Materials and methods: the PubMed database was explored for the literature review, seeking systematic reviews, presentations of clinical cases, clinical and epidemiological studies, using the key words: metaplastic breast carcinoma, metaplastic carcinoma and 2000-2011. Conclusions: histopathologically, metaplastic carcinoma of squamous cells could become presented as a mixture of adenocarcinoma having dominant areas of squamous differentiation and even pure squamous forms, representing the tumor’s phenotypical plasticity. The modified Scarff-Bloom-Richardson system was not applicable regarding this lesion. The most important prognostic factors were age and tumor size; however, some studies considered nodal metastasis and the state of the receptors.


Assuntos
Adulto , Feminino , Neoplasias da Mama , Carcinoma de Células Escamosas , Metaplasia
13.
Salud UNINORTE ; 19: 31-40, jul.-dic. 2004. ilus, tab
Artigo em Espanhol | LILACS | ID: lil-440598

RESUMO

La leptospirosis es una infección sistémica aguda, que da lugar en el hombre a un espectro variablede manifestaciones clínicas, producidas por espiroquetas patogénicas del género leptospira. Es unazooantroponosis de distribución universal, cuyo reservorio lo constituyen animales en especial ratas y perros. La infección en el hombre se produce como consecuenciadel contacto directo con el reservorio animal o indirectamente a través de la exposición de la piellesionada con el agua o en terrenos húmedos contaminados con su deyección. En los humanos produce un cuadro caracterizado por síntomas tipo influenza de apariciónaguda y ruidosa, seguido por dolor abdominal, vómitos, hemorragia subconjuntival, exantema petequialy/o morbiliforme y diarrea. En un 10 por ciento toma un curso dramático con ictericia, manifestacioneshemorrágicas, insuficiencia renal aguda e insuficiencia respiratoria con hemorragia alveolar difusa.Este tipo ictérico severo se reconoce desde 1886 como enfermedad de Weil´s.


The leptospirosis is a sharp infection that gives place to multiple clinical manifestations in the man taken place by espiroquetas of the gender Leptospira.It is a zoonosis of universal distribution that can infect the man in occasions. The reservorio constitutesit wild and domestic animals of species, the dog and the livestocks ovinos, bovine, swinish andequine. The infection to the man takes place accidentally when interfering in the circuit of animalleptospirosis. The infection can take place for direct contact with the animal reservorio or throughthe water or in humid lands (you dilute stagnated, rice fields, tanks).In the humans cause a wide range of symptoms, they include fever it beats, severe headache, chills,mialgias, nauseas, vomits, suffusion of the conjunctive ones, abdominal pain, diarrhea or a rash if theillness non is the patient it can develop renal damage, meningitis, and breathing commitment. Thecup of letalidad is low, but it is directly proportional to th...


Assuntos
Humanos , Masculino , Adulto , Ratos , Saúde , Icterícia , Leptospira interrogans , Leptospirose , Febre , Cefaleia , Oligúria , Saúde Pública
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