ABSTRACT
Abstract Introduction Knowing the information regarding the panorama of lymphoma diagnosis in patients treated in the Brazilian Public Unified Health System from the last 10 years is a challenge for Strategic Health Planning. Objective To characterize the Brazilian population with lymphoma treated in the Brazilian Public Unified Health System between 2008 and 2017 regarding staging, sex, residence site and mortality. Material and methods A descriptive, retrospective, and longitudinal trial with secondary data from DataSUS (SIA/SUS and SIM/SUS) obtained from patients with ICD-10 C81-85. Results There were 70,850 lymphoma cases between 2008 and 2017, of which 55% were male, the median age was 51 years, and 27% had Hodgkin Lymphoma. Most patients (56%) were treated outside the residence city. São Paulo State accounted for 25% of patients. Treatment initiation took more than 60 days in 27% of cases. A total of 45,601 deaths were due to lymphoma (12% Hodgkin Lymphoma and 88% Non-Hodgkin Lymphoma), with a median age 63 years, and were mainly males (55%). Staging data were inadequate in 23% of patients, and analysis was performed only on the valid records. Advanced disease was diagnosed in 58% of patients (60% male; 57% female) and was more common in Non-Hodgkin Lymphoma (62%) versus Hodgkin Lymphoma (49%). Discussion Late diagnosis interferes with mortality rates. Health promotion and cancer prevention campaigns, especially targeting the male public, and training for early diagnosis and early treatment are needed. Conclusion Effective measures for early diagnosis and treatment are urgently needed for lymphoma control.
Subject(s)
Humans , Male , Female , Infant, Newborn , Infant , Child, Preschool , Child , Adolescent , Adult , Middle Aged , Aged , Aged, 80 and over , Young Adult , Hodgkin Disease/diagnosis , Lymphoma/diagnosis , Mortality , Delayed Diagnosis , Neoplasm StagingABSTRACT
Introducción: El trasplante autólogo de progenitores hematopoyéticos es una terapéutica aplicable en determinadas situaciones a pacientes con Linfoma de Hodgkin. Objetivo: Evaluar la respuesta al trasplante autólogo de progenitores hematopoyéticos en los pacientes con Linfoma de Hodgkin. Métodos: Se realizó un estudio de 60 pacientes con Linfoma de Hodgkin trasplantados en el Hospital Clínico Quirúrgico Hermanos Ameijeiras, entre 1991 y 2018. Se estimó el porcentaje de respuesta a los tres meses, la supervivencia global y la supervivencia libre de enfermedad a los cinco años. Resultados: La tasa de respuesta a los tres meses fue de 82,7 por ciento. La supervivencia global y libre de enfermedad a los cinco años fue de 94,7 por ciento y 51,7 por ciento, respectivamente. La mortalidad temprana relacionada con el trasplante fue de 5 por ciento. Conclusiones: La aplicación del trasplante autólogo de progenitores hematopoyéticos constituyó una alternativa terapéutica válida. La baja mortalidad temprana evidenció una realización del procedimiento con un perfil de seguridad satisfactorio(AU)
Introduction: Autologous hematopoietic stem cell transplantation is an applicable therapy in certain situations to patients with Hodgkin's Lymphoma. Objective: To evaluate the response to autologous hematopoietic stem cell transplantation in patients with Hodgkin's Lymphoma. Methods: A study of 60 patients with Hodgkin lymphoma transplanted at Hermanos Ameijeiras Clinical and Surgical Hospital was carried out from 1991 to 2018. The percentage of response at three months, overall survival and disease-free survival period were estimated at five years. Results: The response rate at three months was 82.7 percent. Overall and disease-free survival at five years was 94.7 percent and 51.7 percent, respectively. Early transplant-related mortality was 5 percent. Conclusions: The use of autologous hematopoietic stem cell transplantation was a valid therapeutic alternative. The low early mortality evidenced that the procedure was performed with a satisfactory safety profile(AU)
Subject(s)
Humans , Transplantation, Autologous/mortality , Hodgkin Disease/diagnosis , Hodgkin Disease/therapy , Retrospective StudiesABSTRACT
Introducción: En tiempos de pandemia por COVID-19 toda sintomatología respiratoria o síndrome febril lleva a descartar dicha infección, pero hay que tener en cuenta, sobre todo en pacientes onco-hematológicos, como diagnóstico diferencial la neumonía atípica por Pneumocystis Jirovecii (PCP). Objetivo: Describir el caso de neumonía atípica vs COVID-19 en un paciente con linfoma de Hodgkin. Caso clínico: Paciente mujer de 30 años con diagnóstico de linfoma de Hodgkin tipo clásico estadio clínico III (ECIII), que inicia tratamiento sistémico con quimioterapia esquema R-ABVD (plan de 6 cursos con partes A y B). Recibe 3 cursos R-ABVD con respuesta completa según tomografía. Al programar 4to curso parte B presenta persistencia febril hasta 39,8°C asociado a diaforesis nocturna, que se agudiza en la última semana, por lo que se decide hospitalizarla. Se realiza tomografía contrastada (TEM c/c) de tórax: opacidades en patrón de vidrio deslustrado intercalados con lesiones fibrosas en ambos pulmones, no adenopatías; deshidrogenasa láctica (DHL): 656 UI/L. Sin clínica respiratoria, ni examen físico respiratorio alterado. A descartar PCP vs neumonía COVID-19. Sin leucocitosis, reacción en cadena de polimerasa (PCR) COVID-19 negativa. Se define como neumonía no asociada a coronavirus, por lo que recibe 12 días de antibiótico con Sulfametoxazol + Trimetoprim. A la evolución clínica: mejoría de malestar general y afebril. Finaliza 6 cursos de R-ABVD, con respuesta completa en reevaluación tomográfica, asintomática y presentando prueba rápida para COVID-19 no reactiva. Conclusiones: En el contexto de pandemia por COVID-19 el diagnóstico diferencial debe ser oportuno(AU)
Introduction: In times of COVID-19 pandemic, all respiratory symptoms or febrile syndrome leads to ruling out said infection, but atypical Pneumocystis Jirovecii pneumonia (PCP) must be taken into account, especially in onco-hematological patients, as differential diagnosis. Objective: To describe the case of atypical pneumonia vs. COVID-19 in a patient with Hodgkin's lymphoma. Clinical case report: The case of a 30-year-old female patient with diagnosis of clinical stage III Hodgkin lymphoma (IBD) is reported. She began systemic treatment with R-ABVD chemotherapy scheme (6-course plan with parts A and B). She received 3 R-ABVD courses with complete response according to tomography. When scheduling 4th course, part B, she had feverish persistence up to 39.8 ° C associated with nocturnal diaphoresis, worsening in the last week, so hospitalization was decided. A contrast tomography (TEM c / c) of the thorax was performed: ground-glass opacities interspersed with fibrous lesions in both lungs, no adenopathy; lactic dehydrogenase (DHL): 656 IU / L. No respiratory symptoms, or altered respiratory physical examination, to rule out PCP vs. COVID-19 pneumonia. No leukocytosis, negative COVID-19 polymerase chain reaction (PCR). It is defined as non-coronavirus associated pneumonia, so she received 2 days of Sulfamethoxazole + Trimethoprim antibiotics. On the clinical course, she exhibited improvement of general malaise and she was afebrile. She completed 6 courses of R-ABVD, with complete response in tomographic re-evaluation, she was asymptomatic and had non-reactive rapid test for COVID-19. Conclusions: In the context of COVID-19 pandemic, the differential diagnosis must be timely(AU)
Subject(s)
Humans , Female , Pneumonia, Pneumocystis/etiology , Hodgkin Disease/diagnosis , COVID-19 , Tomography, X-Ray Computed/methodsABSTRACT
RESUMEN Se presentó el caso de una adolescente de 12 años de edad que acudió a consulta externa de Cirugía del Hospital Pediátrico Docente Gral. Pedro Agustín Pérez, de Guantánamo; la misma presentó aumento de volumen a nivel del cuadrante superior externo de la mama izquierda, no doloroso. Se palpó tumoración de bordes irregulares, o sea mal definidos, de 3 cm de diámetro aproximadamente, sin signos de inflamación. Se realizó biopsia por aspiración con aguja fina y se informó el diagnóstico de fibroadenoma de mama. La exéresis del nódulo y el estudio histopatológico demostraron el diagnóstico de linfoma no Hodgkin de alto grado de malignidad y se procedió a la atención multidisciplinaria. Al momento del reporte la paciente continúa con quimioterapia y evoluciona satisfactoriamente. Se revisó la literatura médica sobre el tema y se expusieron sus bases esenciales para la familiarización de los médicos generales.
ABSTRACT A 12 years old young female presented to the surgical outpatient clinic at the Hospital Pediátrico Docente Gral. Pedro Agustín Pérez in Guantanamo. Patient showed swelling in the upper right breast, with no pain. Examination revealed irregular edges (with approximately 3 cm in diameter) and no swollen tissue. Fine-needle aspiration biopsy was performed and breast fibroadenoma was diagnosed. Node exeresis and histopathological study both showed a high risk malignant non-Hodgkin's lymphoma, and a multidisciplinary care team assumed the case. At the time of the report, the patient is still under chemotherapy and prognosis evolves positively. The medical literature on the subject was put on review and a layout of the essentials to familiarize the general practitioners with the topic was set.
Subject(s)
Adolescent , Breast Neoplasms/diagnosis , Hodgkin Disease/diagnosis , Drug Therapy , Fibroadenoma , Biopsy, Fine-NeedleABSTRACT
El linfoma de Hodgkin (LH) recibió su nombre del patólogo británico Thomas Hodgkin, quien en el año 1832 describió varios casos de personas con síntomas de un cáncer que afecta los ganglios linfáticos, denominándose "enfermedad de Hodgkin" durante aproximadamente 170 años. A fines del siglo XX, se determina que esta enfermedad es consecuencia de una lesión en el ADN de un linfocito (un tipo de glóbulo blanco)(1), motivo por el cual es llamada "linfoma de Hodgkin" neoplasia hematológica que en la actualidad constituye uno de los tipos de cáncer más curables.
Subject(s)
Humans , Adolescent , Patient Care Management , Hodgkin Disease/diagnosis , Hodgkin Disease/prevention & controlABSTRACT
ABSTRACT Objective To analyze the prevalence of overweight and the use of conicity index for cardiovascular risk assessment in individuals submitted to autologous hematopoietic stem cell transplantation. Methods The sample comprised 91 patients of both sexes, who underwent autologous hematopoietic stem cell transplantation from September 2008 to December 2013, aged 18 years or over. To determine the nutritional profile, we collected anthropometric data on weight, height, waist circumference upon hospital admission. The body mass index and the conicity index were calculated. Results A total of 91 patients diagnosed with multiple myeloma, Hodgkin's lymphoma, non-Hodgkin's lymphoma and other conditions were evaluated. The mean age was 43.5 (14.2) years, 63.7% were male. We verified that according to the body mass index, 63.7% were overweight and, according to waist circumference, 74.7% had a higher risk for cardiovascular diseases. According to the calculation of the conicity index, 92.3% of patients presented increased cardiovascular risk. Patients with multiple myeloma had a higher conicity index when compared to other patients (p<0.01). Conclusion This study revealed a high prevalence of overweight and cardiovascular risk. It should be noted that the conicity index was a good method to evaluate cardiovascular risk and that new studies using this index should be performed.
RESUMO Objetivo Analisar a prevalência de excesso de peso e a utilização do índice de conicidade para a avaliação do risco cardiovascular em indivíduos submetidos ao transplante autólogo de células-tronco hematopoiéticas. Métodos A amostra foi composta por 91 pacientes, de ambos os sexos, submetidos ao transplante autólogo de células-tronco hematopoiéticas, de setembro de 2008 a dezembro de 2013, com idade igual ou superior a 18 anos. Para traçar o perfil nutricional, foram coletados dados antropométricos, como peso, altura e circunferência da cintura, na admissão hospitalar. Calcularam-se o índice de massa corporal e o índice de conicidade. Resultados Foram avaliados 91 pacientes, diagnosticados com mieloma múltiplo, linfoma de Hodgkin, linfoma não Hodgkin e outras patologias. A média de idade foi de 43,5 (14,2) anos, e 63,7% eram do sexo masculino. Verificou-se que, de acordo com o índice de massa corporal, 63,7% apresentavam excesso de peso e, segundo a circunferência da cintura, 74,7% possuíam maior risco para doenças cardiovasculares. De acordo com o cálculo do índice de conicidade, constatou-se que 92,3% dos pacientes apresentavam risco cardiovascular aumentado. Os pacientes com mieloma múltiplo apresentaram índice de conicidade mais elevado, se comparado aos outros pacientes (p<0,01). Conclusão Este estudo revelou alta prevalência de excesso de peso e de risco cardiovascular. Salienta-se que o índice de conicidade se mostrou um bom método para avaliação do risco cardiovascular e que novos estudos utilizando este índice devem ser realizados.
Subject(s)
Humans , Male , Female , Adult , Aged , Young Adult , Cardiovascular Diseases/etiology , Hematopoietic Stem Cell Transplantation/methods , Transplantation Conditioning/methods , Body Fat Distribution/methods , Obesity/epidemiology , Transplantation, Autologous , Lymphoma, Non-Hodgkin/diagnosis , Brazil/epidemiology , Hodgkin Disease/diagnosis , Cardiovascular Diseases/epidemiology , Body Mass Index , Sex Factors , Prevalence , Risk Factors , Risk Assessment , Overweight/epidemiology , Waist Circumference , Middle Aged , Multiple Myeloma/surgery , Multiple Myeloma/diagnosis , Obesity/complicationsABSTRACT
O linfoma é uma neoplasia originária do sistema linfático, a partir de células linfocitárias. A sintomatologia mais comum é febre, tosse, sudorese noturna, perda de peso, fraqueza e linfoadenopatia indolor. A etiologia ainda permanece desconhecida, tendo sido relacionada ao vírus Epstein-Barr. O diagnóstico se baseia na visualização das células de Reed-Sternberg. O esquema adriamicina, bleomicina, vinblastina e dacarbazina (ABVD) ainda é o tratamento preconizado, associado ou não à radioterapia. Relatamos um caso de linfoma de Hodgkin de apresentação atípica, cujo diagnóstico só foi possível por esplenectomia.(AU)
The lymphoma is a cancer of the lymphatic system originating from lymphocyte cells. The most common symptoms are fever, cough, night sweats, weight loss, weakness, and painless lymphadenopathy. The etiology remains unknown, having been related to the Epstein Barr virus. The diagnosis is based on visualization of Reed Sternberg cells. The adriamycin, bleomicin, vinblastine and dacarbazine (ABVD) regimen is still the preferred treatment, with or without radiation therapy. We report a case of Hodgkin's lymphoma of atypical presentation, the diagnosis of which was only possible through splenectomy.(AU)
Subject(s)
Humans , Male , Aged , Antineoplastic Combined Chemotherapy Protocols , Cyclophosphamide/administration & dosage , Hodgkin Disease/diagnosis , Hodgkin Disease/drug therapy , Reed-Sternberg Cells , Vinblastine/administration & dosageABSTRACT
La Sífilis es una infección adquirida por vía sexual, producida por la bacteria Treponema pallidum. Es una enfermedad crónica sin tratamiento y cursa por etapas con manifestaciones clínicas diferentes en cada una de ellas. Se presenta el caso de un paciente varón de 27 años, que presenta una dermatosis asintomática de 3 semanas de evolución, asociado a importantes adenopatías cervicales dolorosas y a compromiso del estado general, de 2 meses de evolución, lo que en primera instancia fue interpretado como un Linfoma de Hodgkin, y que resultó ser sífilis en etapa secundaria, con buena respuesta al tratamiento convencional de ésta.
Syphilis is a sexually acquired infection caused by the bacterium Treponema pallidum. It is a chronic disease without treatment and is staged in stages with different clinical manifestations in each one of them. Case report of a 27 years old male patient with asymptomatic dermatosis of 3 weeks of evolution, associated with significant painful cervical lymphadenopathy, and systemic symptoms, 2 months of evolution, was first interpreted as a Lymphoma of Hodgkin, and that was syphilis in secondary stage, with good answer to the conventional treatment of this one.
Subject(s)
Humans , Male , Adult , Hodgkin Disease/diagnosis , Syphilis/diagnosis , Early Diagnosis , Lymphadenopathy/diagnosis , Missed DiagnosisABSTRACT
Esta guía esta dirigida al personal de la salud involucrado directamente en la atención de pacientes adultos mayores de 18 años con sospecha o diagnóstico de linfoma no Hodgkin B difuso de célula grande (Linfoma B difuso de células grandes), linfoma folicular (LF), linfoma de células del manto (LCM) y linfoma Hodgkin (LH), y a las instancias administrativas, empresas aseguradoras y entes gubernamentales involucrados en la generación de políticas en salud. Esta GPC basada en la evidencia incluye los temas de diagnóstico y tratamiento del Linfoma B difuso de células grandes, LF, LM y LH, bajo la perspectiva del Sistema General de Seguridad Social en Salud colombiano. Objetivos: Determinar los métodos diagnósticos más apropiados en pacientes con LBDCG para garantizar un diagnóstico preciso que permita una adecuada selección del tratamiento; Establecer las líneas de tratamiento en pacientes con LF para disminuir la heterogeneidad en la atención y mejorar los resultados del tratamiento; Determinar los esquemas de tratamiento de primera línea para pacientes con LCM en diferentes grupos de edad para disminuir la heterogeneidad y mejorar los resultados del mismo; y Mejorar la supervivencia libre de enfermedad y la supervivencia global de los pacientes adultos con LH.
Subject(s)
Humans , Adult , Lymphoma, Non-Hodgkin/diagnosis , Lymphoma, Non-Hodgkin/therapy , Hodgkin Disease/diagnosis , Hodgkin Disease/therapy , Follow-Up Studies , Lymphoma, Follicular/diagnosis , Lymphoma, Follicular/therapy , Lymphoma, Large B-Cell, Diffuse/diagnosis , Lymphoma, Large B-Cell, Diffuse/therapy , Lymphoma, Mantle-Cell/diagnosis , Lymphoma, Mantle-Cell/therapy , GRADE Approach , Neoplasm StagingABSTRACT
Introducción: Las adenopatías son una causa muy frecuente de consulta en la población infantil, estando presente hasta en el 44% de los niños menores de 5 años. En algunos casos se requiere la toma de biopsias ganglionares para esclarecer el diagnóstico. Objetivo: Describir las características clínicas e histopatológicas de pacientes pediátricos con adenopatías sometidos a biopsias ganglionares. Pacientes y método: Estudio descriptivo, retrospectivo. Se incluyó la totalidad de los niños menores de 15 años a los que se les realizó biopsia ganglionar en hospital de alta complejidad en un periodo de 4 años. Se evaluaron las características demográficas, clínicas y de laboratorio de los pacientes, así como el diagnóstico histopatológico de las biopsias realizadas. Resultados: Sesenta y un niños, 54,1%, fueron del sexo masculino, mediana de edad de 6 años. El diagnóstico patológico más frecuente fue hiperplasia reactiva (50,8%), seguido de enfermedad neoplásica (27,9%), enfermedad granulomatosa crónica (4,9%) e infección bacteriana (3,3%). De las enfermedades neoplásicas, el linfoma de Hodgkin fue el más común, siendo su localización más frecuente la cervical (60,6%). Conclusiones: Con este estudio se demuestra la importancia de realización de diagnósticos diferenciales en el abordaje de pacientes con adenopatías. Al igual que lo reportado en la literatura mundial, la etiología benigna es la causa más común de adenopatías en niños.
Background: Lymphadenopathy is a common cause for medical consultation in the child population, accounting for up to 44% in children under 5 years old. In some cases, it is required to take lymph node biopsy specimens in order to clarify the diagnosis. Objective: To describe the clinical and histological features of paediatric patients with lymphadenopathy and lymph node biopsies. Patients and method: Descriptive and retrospective study conducted in Medellin (Colombia) in a fourth-level hospital between January 1st of 2009 and December 31st of 2012. In the study, lymph node biopsy specimens were taken from children under 15 years old. Demographic, clinical and laboratory features, and characteristics of the patients were evaluated, as well as the histopathological diagnosis of the lymph node biopsies. Results: From the child population, 61 children met the eligibility criteria and 33 (54.1%) of them were male with an average age of 6 years old. The most common pathological diagnoses in the study group were as follows: reactive hyperplasia (50.8%), neoplasms (27.9%), chronic granulomatous disease (4.9%), and bacterial infection (3.3%). It could be concluded from the findings in the study that Hodgkin lymphoma is very common among the neoplastic diseases, with 18%, and the most frequent location was the neck with 60.6%. Conclusions: This study demonstrates the importance of performing a differential diagnosis when approaching patients with lymphadenopathy. As reported in the world medical literature, benign origin is the most common cause of lymphadenopathy in children.
Subject(s)
Humans , Male , Female , Child, Preschool , Child , Hodgkin Disease/diagnosis , Lymphadenopathy/diagnosis , Head and Neck Neoplasms/diagnosis , Lymph Nodes/pathology , Biopsy , Retrospective Studies , Diagnosis, Differential , Lymphadenopathy/pathologyABSTRACT
OBJETIVO: analizar las causas de muerte en pacientes con diagnóstico de linfoma de Hodgkin. MÉTODOS: se realizó un estudio retrospectivo-descriptivo en el Servicio de Hematología del Hospital Clinicoquirúrgico "Hermanos Ameijeiras". La muestra quedó constituida por 443 pacientes, de los 619 diagnosticados desde enero de 1983 hasta diciembre del 2008, de ellos 287 (64,8 %) se encontraban vivos al final del estudio y 156 (35,2 %) habían fallecido. RESULTADOS: la recaída/progresión del linfoma de Hodgkin fue la causa más importante de muerte (125 pacientes, 80 %), independiente de la edad de presentación de la enfermedad, la modalidad de tratamiento empleada y el tiempo de evolución. El 20 % restante fue por segundas neoplasias en 10 pacientes (6,4 %), complicaciones del tratamiento en 8 (5,1 %), complicaciones infecciosas fatales en 2 (1,2 %) y enfermedad cardiovascular en 3 (1,9 %). En 8 pacientes (5,1 %) no se precisó la causa de muerte. Predominaron las segundas neoplasias en pacientes de 40-59 años, que recibieron la modalidad de tratamiento combinada y tenían menos de 10 años de evolución. CONCLUSIONES: la recaída/progresión del linfoma de Hodgkin permanece como causa más importante de muerte, independientemente de la edad de presentación, la modalidad de tratamiento empleada y el tiempo de evolución. Sería importante identificar precozmente los casos refractarios al tratamiento convencional para utilizar la modalidad terapéutica más apropiada para la curación.
OBJECTIVE: determine the causes of death in patients diagnosed with Hodgkin lymphoma. METHODS: a retrospective descriptive study was conducted at the Department of Hematology, "Hermanos Ameijeiras" Hospital. The sample was composed of 443 patients, 619 diagnosed from January 1983 to December 2008. 287 of them (64.8 %) were alive at the end of the study, 156 (35.2 %) had died. RESULTS: the relapse/progression of Hodgkin lymphoma was the most important cause of death (125 patients, 80 %), regardless of the age of the disease onset, the type of treatment used and the time of evolution. The remaining 20 % was due to: second malignancies in 10 patients (6.4 %), complications of treatment in 8 (5.1 %), fatal infectious complications in 2 (1.2 %) and cardiovascular disease in 3 (1.9 %). In 8 patients (5.1 %) the cause of death was not specified. Secondary malignancies prevailed in patients aged 40-59 years who received combined treatment and had less than 10 years of evolution. CONCLUSIONS: relapse/progression of Hodgkin lymphoma remains a leading cause of death, regardless of the onset age, the treatment modality used and the time of evolution. It would be important to identify early cases refractory to conventional treatment to use the most appropriate therapeutic modality for healing.
Subject(s)
Humans , Hodgkin Disease/diagnosis , Hodgkin Disease/mortality , Neoplasm Recurrence, Local , Recurrence , Epidemiology, Descriptive , Retrospective StudiesABSTRACT
Aim: to identify the leisure activities performed in Long-Stay Institutions for the Elderly (LSIEs), registered in the city of Maringá-PR, Brazil, and to analyze the attitude of the elderly people toward leisure promoted by the institutions. METHOD: this was a descriptive and transversal study with a quantitative approach, carried out with 97 elderly people, through the establishment of the socio-demographic profile and the application of the Leisure Attitude Scale. The data was subjected to descriptive statistical analysis, association tests (chi-square or Fisher's) and Spearman's correlation. RESULTS: males, aged 80 or over, widowed, with one to eight years of study, who had a monthly income were predominant. Age group and income were significantly associated with the performance of leisure activities. The results reflected the positive attitude of the elderly people in relation to leisure activities, except in the behavioral component. CONCLUSION: the findings of this study indicate the need for further investigation into the difficulties linked to the attitude toward leisure in the behavioral component, considering aspects such as individual concepts of leisure and the health status of the elderly people. .
OBJETIVOS: identificar as atividades de lazer realizadas em Instituições de Longa Permanência para Idosos (ILPI), regularmente cadastradas no município de Maringá - PR, Brasil, e analisar a atitude dos idosos face ao lazer promovido pelas instituições. MÉTODO: trata-se de uma pesquisa de caráter descritivo e transversal, com abordagem quantitativa, realizada com 97 idosos, por meio de levantamento do perfil sociodemográfico e da aplicação da Escala de Atitudes Face ao Lazer. Os dados passaram por análise estatística descritiva, testes de associação (quiquadrado ou Fisher) e correlação de Spearman. RESULTADOS: predominaram homens, na faixa etária de 80 anos ou mais, viúvos, com um a oito anos de estudo e que possuíam renda mensal. Faixa etária e renda tiveram associação significativa com a realização de atividades de lazer. Os resultados refletiram atitude positiva dos idosos em relação às atividades de lazer, exceto no componente comportamental. CONCLUSÃO: os achados deste estudo indicam a necessidade de investigação das dificuldades atreladas à atitude face ao lazer no componente comportamental, considerando aspectos como concepções individuais de lazer e condição de saúde dos idosos. .
OBJETIVOS: identificar las actividades de ocio o tiempo libre realizadas en Instituciones de Larga Permanencia para Ancianos (ILPA) regularmente registradas en el municipio de Maringá-PR, Brasil, y analizar la actitud de los ancianos frente al tiempo libre promovido por las instituciones. MÉTODO: se trata de una investigación de carácter descriptivo y transversal, con abordaje cuantitativo, realizada con 97 ancianos, por medio del levantamiento del perfil sociodemográfico y de la aplicación de la Escala de Actitudes Frente al Ocio. Los datos pasaron por análisis estadístico descriptivo, test de asociación (chi-cuadrado o Fisher) y correlación de Spearman. RESULTADOS: predominaron hombres, en el intervalo etario de 80 años o más, viudos, de uno a ocho años de estudio y que poseían renta mensual. El intervalo etario y la renta tuvieron asociación significativa con la realización de actividades de tiempo libre. Los resultados reflejaron una actitud positiva de los ancianos en relación a las actividades de tiempo libre, excepto en el componente comportamental. CONCLUSIÓN: los hallazgos de este estudio indican la necesidad de investigar las dificultades vinculadas a la actitud frente al tiempo libre en el componente comportamental, considerando aspectos como las concepciones individuales de tiempo libre y la condición de salud de los ancianos. .
Subject(s)
Humans , Male , Female , Child, Preschool , Child , Adolescent , Adult , Hodgkin Disease/diagnosis , Hodgkin Disease/mortality , Hodgkin Disease/therapy , Disease-Free Survival , Follow-Up Studies , Recurrence , Retrospective Studies , Survival RateABSTRACT
La dermatitis flagelada es una entidad caracterizada por la presencia de máculas eritematopigmentadasde disposición lineal, localizadas a predominio del tronco. Descrita inicialmente como reacción adversa a la bleomicina, existen comunicaciones de otros fármacos implicados. También se la ha observado por ingesta de hongos shiitake y en el contexto de la dermatomiositis. Presentamos seis pacientes con clínica e histopatología compatibles con dermatitis flagelada:cuatro en tratamiento quimioterápico con bleomicina (tres mujeres y un hombre, de entre 20 y 40 años; con diagnóstico de linfoma Hodgkin, coriocarcinoma uterino y seminoma testicular). El quinto caso corresponde a una mujer de 46 años, con diagnóstico de LES que desarrolló las lesiones luego de recibir azatioprina. Y el sexto paciente masculino, de 60 años, que presentó una dermatitis flagelada en el contexto de una dermatomiositis amiopática...
Subject(s)
Humans , Male , Adult , Female , Bleomycin , Hodgkin Disease/diagnosis , Azathioprine , DermatomyositisABSTRACT
Primary Pulmonary Lymphomas (LPP) are infrequent and their clinical manifestations and images are usually non specific. Diagnostic delay may be important. The objective of this study was to analyze the LLP in our institution. Between 2003 and 2013, over 1,892 lymphomas were analyzed in our institution. Only 4 of them (0.21 percent incidence) were detected as LPP: Non Hodgkin's Lymphoma (n = 2), Hodgkin's Lymphoma (n = 1), and Intravascular Pulmonary Lymphoma (n = 1). Clinical manifestations of the 4 cases presented were unspecific: 1) pulmonary mass and pleural effusion; 2) consolidation with air bronchogram and cavitations; 3) normal images and 4) pulmonary mass. Given these clinical settings, 4 diagnostic methods were used: 1) Computed Tomography-Guided Puncture, 2) Video-Assisted Thoracoscopic Surgery (VATS); 3) VATS guided by positron emission tomography (PET) and 4) thoracotomy. Hence, diagnosis was successfully made between 45 to 90 days from the initial consultation. This report confirms the low incidence of LPP, and its unspecific clinical and radiographic manifestations that may cause delay in diagnosis. PET can contribute to improve diagnostic performance, especially in patients without apparent lung involvement.
Los linfomas primarios de pulmón (LPP) son infrecuentes. Sus manifestaciones clínicas y las imágenes son inespecíficas. El retraso diagnóstico puede ser considerable. Objetivo: Analizar los LPP durante el período 2003-2013 en nuestra institución. Sobre 1892 linfomas, 4 fueron LPP (0,21 por ciento): 1) linfoma no Hodgkin (n = 2); 2) linfoma Hodgkin (n= 1); 3) linfoma intravascular pulmonar (n = 1). Las manifestaciones clínicas y radiológicas fueron inespecíficas (masa pulmonar y derrame pleural, consolidación con broncograma aéreo y cavitación o bien ausencia de lesiones). Los métodos diagnósticos fueron: 1) punción guiada bajo TAC; 2) videotoracoscopía (VATS) y 3) VATS orientada por PET (tomografia por emisión de positrones) y 4) toracotomía. El tiempo entre la consulta inicial hasta el diagnóstico fue de 45 a 90 días. Este reporte confirma la baja incidencia de LPP, y sus manifestaciones clínicas y radiologías poco específicas. Esto puede contribuir a las demoras en el diagnóstico. El PET puede mejorar el rendimiento diagnóstico, en especial en ausencia de compromiso pulmonar radiológico evidente.
Subject(s)
Humans , Male , Adult , Female , Aged , Lymphoma/diagnosis , Lung Neoplasms/diagnosis , Hodgkin Disease/diagnosis , Lymphoma, Non-Hodgkin/diagnosis , Lymphoma/therapy , Lung Neoplasms/therapy , Positron-Emission Tomography , Tomography, X-Ray ComputedABSTRACT
O vírus de Epstein Barr (EBV) é o agente causador da mononucle¬ose infecciosa e está associado a várias desordens proliferativas malignas tais como: linfoma de Burkitt, linfoma de Hodgkin e lin¬fomas não Hodgkin. Objetivo: detectar o genoma do EBV mediante a identificação dos genes EBER1 e EBNA1 em casos de doença de Hodgkin. Métodos: um total de 65 casos de linfomas diagnosti¬cados no Hospital Ophir Loyola no período de 1996 e 2005 foram analisados no Instituto Evandro Chagas, Ananindeua, Brasil. Todos os espécimes parafinizados foram analisados por hibridização in situ (gene EBER1) e PCR em tempo real (EBNA1). Resultados: do total, 64,6% (42/65) dos pacientes eram do sexo masculino e 35,4% (23/65) do sexo feminino. O EBV foi identificado por HIS nas células Reed Sternberg e variantes em 76,9% (50/65) dos casos com idade média de 28,3 anos (variação 2-84 anos). Os subtipos histológicos de casos EBV-positivos foram os seguintes: esclerose nodular em 50% (25/50), celularidade mista em 28% (14/50), depleção linfocitária em 14% (7/50) e predominância linfocitária em 8% (4/50). O DNA do EBV foi detectado em 53% (26/49) dos casos de doença de Hodgkin com um coeficiente de regressão para a curva padrão de 0,99. Conclusão: este estudo foi a primeira descrição do vírus de Epstein Barr em casos de linfoma de Hodgkin na Amazônia Brasileira, reforçando a hipótese de que o EBV seja um co-fator no processo de transformação neoplásica em conjunto com a predisposição genética e imunidade do paciente
Introduction: EBV is the causative agent of infectious mononucleosis and is associated with several malignant proliferative disorders such as Burkitts lymphoma, Hodgkins lymphoma, some B and T cell non-Hodgkins lymphomas. Objective: The main objective of the study was to determine the prevalence of EBER 1 gene and EBNA1 gene in cases of Hodgkins disease. Material and Methods: A total of 65 cases of lymphomas diagnosed between 1996 and 2005 were obtained from Instituto Ofir Loyola and analyzed at the Instituto Evandro Chagas Ananindeua, Brazil. The EBV antigens using EBER 1 probe in situ hybridization (HIS) and real time quantitative PCR. Results: From the total obtained, 64.6% (42/65) were male and 35.4% (23/65) female. EBV was identified in the Reed- Sternberg cells and variants in 76.9% (50/65) of Hodgkins disease cases, the median age were 28.3 years (range 2-84). The histologic subtypes of EBV-positive cases were as follows: nodular sclerosis in 50% (25/50), mixed cellularity in 28% (14/50), lymphocyte depletion in 14% (7/50) and lymphocyte predominance in 8% (4/50). We detected EBV DNA in 53% (26/49) with a coefficient of regression for the standard curve of a minimum of 0.99. Conclusion: These results were the first demonstration of the role of Epstein Barr virus in cases of Hodgkin diseases in northern Brazil and are consistent with the hypothesis that the presence of EBV during neoplasic transformation could be an additional cofactor acting together with both genetic predisposition and immunity of the patient
Subject(s)
Male , Female , Humans , Hodgkin Disease/diagnosis , Hodgkin Disease/history , Genome, Viral , In Situ Hybridization , Real-Time Polymerase Chain ReactionABSTRACT
El linfoma de Hodgkin (LH) es una neoplasia del sistema linfático. La incidencia mundial anual del LH es de 3-10/100,000 habitantes. El mecanismo mediante el cual se lleva a cabo la transformación celular no es completamente claro; sin embargo, algunas evidencias parecen indicar que ciertos virus oncogénicos como el virus Epstein Barr (VEB), pueden tener alto impacto en la patogénesis de la linfoproliferación. También algunos factores genéticos y ambientales pueden estar involucrados, pues se ha encontrado una alta incidencia de casos de LH entre individuos de una misma familia que comparten características genéticas y conviven en un mismo ambiente. En México se han realizado estudios encaminados a conocer la prevalencia del VEB en pacientes con LH y se ha encontrado la presencia de este virus hasta en el 64,2%. El VEB ha sido detectado en las Células Reed Sternberg (CRS) y en Células de Hodgkin (CH) en el 50% de los casos de LH clásico. No se ha dado hasta ahora una explicación satisfactoria, pero se ha propuesto que la variabilidad geográfica y la variabilidad inmunológica desempeñan un papel determinante en la positividad del VEB en LH. A pesar de los avances que hasta ahora se tienen, no existen suficientes evidencias que permitan establecer una clara asociación entre los factores del huésped, el medio ambiente y el agente patógeno en el riesgo de la linfoproliferación que conduce al desarrollo de LH. La presente revisión tiene como objetivo analizar algunos de los factores de riesgo que influyen durante la interacción huésped, agente patógeno y medio ambiente en la etiología del LH.
Hodgkin lymphoma (HL) is a neoplasm characterized by malignant cells called Reed Sternberg and Hodgkins cells in the lymphatic system. Such cells comprise 1% of the tumor while the remainder is made up of lymphocytes, histiocytes, eosinophils and plasma non-neoplastic cells. The annual global incidence of HL is 3-10/100,000 inhabitants and is most commonly found in young adults. The mechanism by which cell transformation is accomplished is not entirely clear; however, some evidences suggest that oncogenic viruses like the Epstein Barr virus (EBV) may have a high impact on the pathogenesis of lymphoproliferation. Genetic and environmental factors could be involved, since it has been found a high incidence of HL among members of the same family. In Mexico, there have been studies to determine the prevalence of EBV in patients with HL and found the presence of this virus in up to 64.2% of the cases. EBV has been detected in the Reed Sternberg cells and Hodgkin cells in 50% of cases of classical HL. There is not a satisfactory explanation for this, but it has been proposed that geographic and immunological variabilities play a role in the positivity of EBV in HL. However, despite recent advances in the field, there is insufficient evidence to show a clear association between host factors, environment and pathogens, and the risk of lymphoproliferation leading to the development of HL. This review aims to give an overview about the risk factors that influence the interaction of host, pathogens and environment in the etiology of HL.
Subject(s)
Female , Humans , Male , Epstein-Barr Virus Infections/virology , Host-Pathogen Interactions , /physiology , Hodgkin Disease/virology , Biomarkers, Tumor , Cell Transformation, Viral , DNA, Viral/genetics , Epstein-Barr Virus Infections/immunology , Gene Expression Regulation, Viral , /genetics , /immunology , Hodgkin Disease/diagnosis , Hodgkin Disease/epidemiology , Immune Evasion , Immunocompromised Host , Risk , Risk Factors , Reed-Sternberg Cells/virology , Virus Latency , Viral Proteins/physiologyABSTRACT
Superior Cava Venous Syndrome (SVCS) encompasses a constellation of signs and symptoms resulting from partial or complete obstruction of blood flow through the superior vena cava (SVC) to the right atrium. Thrombosis can be caused by intrinsic (primary) or extrinsic compression (with or without secondary thrombosis). The causes of SVCS can be grouped according to their etiology in non-neoplastic and neoplastic. The causes malignant correspond to 65-90
of them, thrombosis and nonmalignant conditions are another causes. The presentation may be acute, clinically characterized by dyspnea and a characteristic triad (facial, neck and arms edema, cyanosis and collateral circulation). Early detection improves prognosis and is based on clinical data and imaging studies. We describe 8 cases where the SVCS was the first manifestation of neoplastic diseases. Patients were predominantly of middle-aged, male, without association with consumption of tobacco and lymphoma was most frequent diagnosis.
Subject(s)
Hodgkin Disease/complications , Lymphoma, Non-Hodgkin/complications , Superior Vena Cava Syndrome/etiology , Adolescent , Adult , Young Adult , Early Diagnosis , Hodgkin Disease/diagnosis , Female , Humans , Lymphoma, Non-Hodgkin/diagnosis , Male , Mediastinoscopy , Middle Aged , Superior Vena Cava Syndrome/diagnosisABSTRACT
This study was designed to identify factors that can predict bone marrow involvement [BMI] by bone marrow biopsy [BMB] in Hodgkin's lymphoma [HL]. Patients of both sexes [35 males and 22 females] with Hodgkin's lymphoma who were admitted to Aleppo University Hospital and Al-Kindi University Hospital were enrolled in the period from May 2010 to May 2012. All patients had received bilateral bone marrow biopsy, the relationships between BMB results and other clinical and laboratory features were studied completely. Seven patients [12.3%] showed to have BMI [2 in one side, 5 in both]. The factors that predict BMI were: B symptoms, iliac and/or inguinal lymphadenopathy, involvement of >/= 4 lymphatic areas, lymphocyte depleted [LD] histology, advanced stages [3 and 4], lymphocytopenia [<1000/mm[3]], eosinophilia [>400/mm[3]], anemia and elevated ESR [>50 mm/1[st] h]. The probability of BMI according to the presence of these variables was 0% for [0 to 6] factors, 75% for 7 factors and 100% for 8 or 9 of the previous factors. Bilateral BMB is recommended in patients who have more than 6 of the previous factors