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Texto completo SciELO Cuba
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Id: lil-787210
Autor: Rodríguez Morales, José Ramón; Chaviano Jiménez, Leopoldo; Hernández Cruz, Julio Orlando.
Título: Sarcoma sinovial: a propósito de dos pacientes / Synovial sarcoma: a report of two cases
Fonte: Medicentro (Villa Clara);20(3):223-228, jul.-set. 2016.
Idioma: es.
Descritores: Sarcoma Sinovial
Responsável: CU425.1 - Centro Provincial de Información de Ciencias Médicas de Villa Clara


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Id: lil-734316
Autor: Farfalli, Germán Luis; Iriberry, Ángeles; Albergó, José Ignacio; Ayerza, Miguel Ángel; Muscolo, Domingo Luis; Aponte-Tinao, Luis Alberto.
Título: Sarcomas de partes blandas en pacientes pediátricos: análisis de una serie de casos del subtipo no rabdomiosarcoma / Pediatric soft tissue sarcomas: analysis of non rhabdomyosarcoma group
Fonte: Arch. argent. pediatr;112(6):e257-e261, dic. 2014. ilus, tab, graf.
Idioma: es.
Resumo: Se evaluó una serie de 29 pacientes con diagnóstico de sarcomas de partes blandas variante no rabdomiosarcomas tratados quirúrgicamente entre2000 y 2010, y se analizó la supervivencia global y los factores que influyen en el pronóstico. La edad media fue de 11,6 años (rango de 3 meses-17 años); 16 pacientes eran de sexo masculino y el tiempo promedio de seguimiento fue de 56 meses (de 8 a 132 meses). Se documentaron 8 variedades histológicas diferentes de tumores malignos, y el sarcoma sinovial resultó ser el más frecuente (14 pacientes). La cirugía de conservación de miembro fue posible en 28 pacientes y se asoció tratamiento adyuvante en 26. La supervivencia global de la serie estudiada fue de 72% a los 5 años y, en 9 pacientes, se diagnosticó una recurrencia local. La presencia de metástasis (p < 0,0001) y la recurrencia local (p < 0,007) resultaron ser factores de pronóstico negativo para la supervivencia global.

We evaluated 29 patients with non rhabdomyosarcoma soft tissue sarcomas treated with surgery between 2000 and 2010; we analyzed overall survival and which factors affect the prognosis. The mean age was 11.6 years (range 3 months-17 years); 16 patients were males and the median follow-up was 56 months (8 to 132 months). Eight different histological malignant tumors were identified, being synovial sarcoma the most prevalent one (14 patients). Twenty-eight patients were treated with limb salvage surgery and in 26 cases, adjuvant therapy was used. Five years overall survival was 72%. Nine of the 29 patients presented a local recurrence. The presence of metastases (p <0.0001) and local recurrence (p <0.007) were negative prognostic factors for overall survival.
Descritores: Pediatria
Neoplasias de Tecidos Moles
Sarcoma Sinovial
Sobrevivência
Recidiva Local de Neoplasia
Limites: Seres Humanos
Tipo de Publ: Relatos de Casos
Responsável: AR94.1 - Centro de Información Pediatrica


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Id: biblio-987342
Autor: Vitagliano, Gonzalo Juan; Blas, Leandro; Ringa, Maximiliano; Rios Pita, Hernando; López, Francisco Miguel; Ameri, Carlos Alberto.
Título: Sarcoma sinovial renal primario: reporte de caso y revisión de la literatura / Primary Renal Synovial Sarcoma: Case Report and Literature Review
Fonte: Rev. argent. urol. (1990);83(3):115-117, 2018. ilus..
Idioma: es.
Descritores: Sarcoma Sinovial/cirurgia
Sarcoma Sinovial/diagnóstico
Neoplasias Renais/cirurgia
Neoplasias Renais/diagnóstico
-Imuno-Histoquímica/métodos
Tomografia Computadorizada por Raios X
Ultrassonografia
Resultado do Tratamento
Laparoscopia
Nefrectomia/métodos
Limites: Seres Humanos
Masculino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: AR305.1 - SID - Servicio de Información y Documentación


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Id: biblio-834336
Autor: Lopes, Luiz Carlos; Giusti, André Luis; Inglez, Thaís Daltoé; Raimundo, Elean Lamar; Souza, Gustavo Barbosa de.
Título: Sinoviosarcoma de tornozelo: quarta recidiva / Ankle's synoviosarcoma: fourth relapse
Fonte: Rev. HCPA & Fac. Med. Univ. Fed. Rio Gd. do Sul;30(2):163-165, 2010. ilus.
Idioma: pt.
Resumo: Esse relato apresenta o caso de uma paciente com quarta recidiva de sinoviosarcoma, um sarcoma de partes moles que possui estreita relação com bainhas tendinosas, bursas e cápsulas articulares. A paciente apresentou uma quarta recidiva, sendo necessária a realização da amputação de perna, visto que as cirurgias conservadoras já não aliviam o sofrimento da paciente. O principal objetivo deste relato de caso é apresentar um caso clássico de neoplasia rara, expondo a doença e fazer uma breve revisão da literatura e mostrar sua importância, visto que corresponde a apenas 5% das neoplasias de partes moles.

This report presents the case of a female patient with fourth synoviosarcoma recurrence, a sarcoma of soft parts that have close relationship with tendom sheaths, bursas and articular capsule.The patient present her fourth recurrence, in wich the perfomance of amputation was required, since the conservative surgeriesno longer relieved the patient suffering. The main objective of this case report is to present a classic case of a rare cancer, exposing the disease, and to make a brief review of the literature to show its importance, since it corresponds to only five percent of the cancers of soft parts.
Descritores: Sarcoma Sinovial/diagnóstico
Sarcoma Sinovial/terapia
Tornozelo/patologia
-Amputação
Neoplasias de Tecidos Moles/diagnóstico
Neoplasias de Tecidos Moles/terapia
Prognóstico
Recidiva Local de Neoplasia
Resultado do Tratamento
Limites: Seres Humanos
Feminino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: BR18.1 - Biblioteca FAMED/HCPA


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Id: biblio-986529
Autor: Castrillón, Mauricio Estrada; Mejía Gómez, Catalina; Gil Serrano, Patricia Eugenia; Franco Cano, Mauricio; Carrascoso Arranz, Javier.
Título: Sarcoma sinovial monofásico de tipo fibroblástico. Evaluación diagnóstica por RM y postratamiento mediante ADC: Presentación de un caso / Monophasic Fibroblastic Synovial Sarcoma. Diagnostic and Post-Treatment Assessment by MRI and ADC: Case Report
Fonte: Rev. colomb. radiol;28(4), 2017. ilus.
Idioma: es.
Resumo: El sarcoma sinovial representa entre el 2 al 10 % de todas las malignidades primarias de tejidos blandos, situándose en el cuarto lugar en frecuencia de los sarcomas de tejidos blandos. Es una neoplasia clasificada por la WHO (World Health Organization) bajo la categoría de tumores de diferenciación incierta, considerándose una malignidad entre intermedio y alto grado. El tratamiento estándar es la escisión quirúrgica, sin embargo, por su alta recurrencia y en los casos en que se asocia a metástasis o márgenes positivos después de la resección, se han planteado otros tratamientos como la quimio y radioterapia. La imaginología juega un papel importante en el diagnóstico, la estadificación y evaluación de la respuesta al tratamiento. Nuevas técnicas como el uso de difusión y mapas de ADC (Apparent Diffusion Coefficient, o coeficiente de difusión aparente) en resonancia magnética (RM) son útiles para evaluar las lesiones tumorales y la respuesta al tratamiento. En este artículo se presenta el caso de un paciente con un sarcoma sinovial monofásico, el diagnóstico por imágenes y evaluación del tratamiento mediante técnicas avanzadas de resonancia magnética como la difusión

Synovial sarcomas represent 2 to 10% of all the primary tissue malignancies and occupy the fourth place in the list of most common soft tissue sarcomas. According to the World Health Organization (WHO), this neoplasm is classified under the category of tumors of uncertain differentiation and is considered an intermediate to high-grade malignancy. Although the standard treatment is surgical excision, alternative treatments such as radiotherapy and chemotherapy have been proposed due to its high rate of recurrence in cases when it is associated with metastasis or positive resection margins. Imaging plays a key role in the diagnosis, staging and assessment of treatment of this disease. New techniques in Magnetic Resonance Imaging such as diffusion and Apparent Diffusion Coefficient (ADC) mapping are useful to further characterize these neoplastic lesions and to assess treatment response. In this article we present a patient with monophasic synovial sarcoma in which the use of these new imaging techniques was essential for the diagnosis and evaluation post-treatment.
Descritores: Diagnóstico por Imagem
-Imagem por Ressonância Magnética
Sarcoma Sinovial
Limites: Seres Humanos
Responsável: CO371.9


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Texto completo SciELO Chile
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Id: lil-762627
Autor: García-Morato, Joaquín; Damonte, Alejandro; Rossetti, Noelia S; Arribalzaga, Eduardo B.
Título: Evolución infrecuente de sinoviosarcoma de muslo / Uncommon evolution after excision of a thigh synovial sarcoma
Fonte: Rev. chil. cir;67(5):527-530, oct. 2015. ilus.
Idioma: es.
Resumo: Background: Synovial sarcoma is a soft tissue tumor with a high degree of local and metastatic invasion. Case report: We report a 26 years old smoker woman with a history of a synovial tumor excised from the right thigh, who required a hip prosthesis for a pathological fracture due to metastases. Two years after, a lung metastasis in the left upper lobe was excised and treated with chemo and radiotherapy. Two years later a new lung nodule was found and excised. Pathology confirmed that they were metastases of the primary tumor. Three months after this last excision, the patient is asymptomatic.

Introducción: El sinoviosarcoma es una neoplasia de partes blandas con alto grado de invasión local y producción de metástasis. Caso clínico: Mujer de 26 años con 2 episodios secuenciales de metástasis pulmonar a lo largo de 6 años posterior al tratamiento del tumor primario. Patología de tratamiento muy complejo.
Descritores: Neoplasias Pulmonares/cirurgia
Neoplasias Pulmonares/secundário
Neoplasias de Tecidos Moles/patologia
Sarcoma Sinovial/cirurgia
Sarcoma Sinovial/secundário
-Coxa da Perna
Limites: Seres Humanos
Adulto
Feminino
Tipo de Publ: Relatos de Casos
Responsável: CL1.1 - Biblioteca Central


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Texto completo SciELO Brasil
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Id: lil-720780
Autor: Maia, Daniela Cristina Caetano; Menezes, Carla Kellen da Silva; Bastos, Thales Costa; Ferreira, Luiz Carlos de Lima; Francesconi, Fabio.
Título: Poorly differentiated synovial sarcoma in the wrist - Case report
Fonte: An. bras. dermatol;89(5):816-818, Sep-Oct/2014. graf.
Idioma: en.
Resumo: Synovial sarcomas are rare malignant tumors affecting mainly young adults, presenting as a slow growth mass located in deep soft tissues of extremities, near the joints. In this report a 34-year-old male patient, presented an ulcerovegetative lesion on the right wrist which was completely excised. Histopathology and immunohistochemistry confirmed synovial sarcomas with poorly differentiated cells. This patient presented 11 months later with ipsilateral axillary lymph node metastasis, which emphasizes the unfavorable prognosis of this synovial sarcoma variant. The indolent growth pattern of this sarcoma justifies the well circumscribed initial stages, which progressively infiltrate adjacent structures with lung metastasis (80%) and lymph node involvement (20%) and thus corroborates the importance of early diagnosis and proper treatment.
Descritores: Sarcoma Sinovial/patologia
Pele/patologia
Neoplasias de Tecidos Moles/patologia
Punho
-Biópsia
Imuno-Histoquímica
Limites: Adulto
Seres Humanos
Masculino
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


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Texto completo SciELO Brasil
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Id: lil-709751
Autor: Fonseca, Adriano Santana; Azevedo, Amanda Canário Andrade; Magalhães, Fabíola Moreira; Andrade, Nilvano Alves de.
Título: Synovial Sarcoma in Head and Neck: A Case Report
Fonte: Int. arch. otorhinolaryngol. (Impr.);18(1):87-89, 01/2014.
Idioma: en.
Resumo: Introduction: Synovial sarcoma is a malignant tumor of mesenchymal pluripotent cells. Objectives: We present a case of synovial sarcoma in the posterolateral wall of the oropharynx. Resumed report: The patient, a 23-year-old woman, was admitted with a history of dysphagia and difficulty in breathing for 8 months, resulting in progressive deterioration and onset of snoring, muffled voice, and local pain. An oropharyngeal tumor in the left posterolateral wall touched the base of the ipsilateral tongue. The patient underwent endoscopic pharyngectomy to remove the lesion. Pathologic examination revealed synovial sarcoma with positive margins, and Mohs technique was proposed for margin control. The margins were disease-free, without the need for total laryngectomy. The pharynx was reconstructed with a microvascular forearm flap. The patient developed postoperative stability. Conclusion:  Despite its name, synovial sarcoma is rarely sourced directly from synovial membranes. It is most commonly found in the vicinity of large joints. The location at the head and neck, a location poor in synovial tissue, is unusual. Synovial sarcoma in the head and neck has an aggressive nature and poor prognosis. Resection with negative margins remains the foundation of therapy, which is not so easily achieved in the head and neck. It is important for the otorhinolaryngologist and head and neck surgeon to be familiar with this aggressive tumor, which carries high mortality and morbidity. The appropriate diagnosis and treatment can improve prognosis and patient survival...
Descritores: Transtornos de Deglutição
Neoplasias de Cabeça e Pescoço
Sarcoma Sinovial
-Diagnóstico
Terapêutica
Limites: Seres Humanos
Feminino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: BR66.1 - Divisão de Biblioteca e Documentação


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Texto completo SciELO Brasil
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Id: lil-701278
Autor: Bezerra, Sabrina Godoy; Brandão, Andrea Araújo; Albuquerque, Denilson Campos; Militão, Rochelle Coppo; Hadlich, Marcelo Souza; Azevedo, Clerio Francisco.
Título: Sarcoma pericárdico de células sinoviais: relato de caso e revisão da literatura / Pericardial synovial sarcoma: case report and literature review
Fonte: Arq. bras. cardiol;101(6):e103-e106, dez. 2013. ilus.
Idioma: pt.
Descritores: Neoplasias Cardíacas/patologia
Pericárdio/patologia
Sarcoma Sinovial/patologia
-Ecocardiografia
Evolução Fatal
Neoplasias Cardíacas/cirurgia
Imagem por Ressonância Magnética
Necrose
Invasividade Neoplásica
Prognóstico
Derrame Pericárdico/patologia
Pericárdio/cirurgia
Sarcoma Sinovial/cirurgia
Limites: Adulto
Feminino
Seres Humanos
Tipo de Publ: Relatos de Casos
Revisão
Responsável: BR1.1 - BIREME


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Id: lil-661851
Autor: Romero Rojas, Alfredo Ernesto; Restrepo Escobar, Ligia Inés; Melo-Uribe, Mario Alexánder; Díaz-Pérez, Julio Alexánder.
Título: Sarcoma sinovial digital / Digital Synovial Sarcoma
Fonte: Rev. colomb. cancerol;13(3):175-180, sept. 2009. tab, graf.
Idioma: es.
Resumo: El sarcoma sinovial es una entidad bien definida clínica y morfológicamente y, a pesar de su nombre, es muy raro en las cavidades articulares. Este sarcoma afecta zonas sin relación aparente con las estructuras sinoviales y representa entre el 5% y el 10% de todos los sarcomas de los tejidos blandos. Se encuentra con mayor frecuencia en las extremidades, especialmente en las inferiores, donde tiende a localizarse en la vecindad de las grandes articulaciones; se han informado muy pocos casos de sarcomas sinoviales en las manos o los pies, con una evolución clínica favorable. Así mismo, es más frecuente de 15 a 40 años de edad (con una edad media de 34 años). Este artículo presenta el caso de una mujer adulta a quien se le realizó el diagnóstico histopatológico e inmunohistoquímico de un sarcoma sinovial en el quinto dedo de la mano derecha.

Synovial sarcoma is a clinically and morphologically well defined entity which, in spite of its name, is rare in joint cavities. This sarcoma affects zones without any apparent relation to synovial structures and represents from 5% to 10% of all sarcomas in soft tissues. It is most frequently found in the extremities, especially the lower ones, where it tends to be located in the vicinity of the major articulations; there are very few favorable reports on the clinical evolution of synovial sarcomas in the hands or feet. It is most frequent between the ages of 15 to 40 (median age, 34). This article presents the case of an adult woman who underwent histopathologic and immunohistochemical diagnosis of a synovial sarcoma on the little finger of her right hand.
Descritores: Extremidade Inferior
Sarcoma
Sarcoma Sinovial
-Colômbia
Imuno-Histoquímica/métodos
Limites: Seres Humanos
Adolescente
Adulto
Feminino
Tipo de Publ: Relatos de Casos
Responsável: CO40.1 - Biblioteca Médica



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