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Pesquisa : D23.050.301.264.900 [Categoria DeCS]
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Id: lil-699011
Autor: Lage, Thaiane Lima; Miranda, Mario Fernando Ribeiro de; Bittencourt, Maraya de Jesus Semblano; Dias, Carolina Moraes; Parijos, Amanda Magno de; Raiol, Theisla Kely Azevedo.
Título: Case for diagnosis / Caso para diagnostico
Fonte: An. bras. dermatol;88(6):1005-1007, Nov-Dec/2013. graf.
Idioma: en.
Resumo: Granular cell tumor is a rare benign neoplasm of neural origin. We report the case of a female patient, 27 years old presenting a brown-red nodule in the right arm, which pathological examination showed to be formed by polygonal cells with eosinophilic granular cytoplasm and immunohistochemistry positive for S100 protein and CD68. Granular cell tumor is usually solitary and in half the cases located in the head and neck areas, 30% of these in the tongue. It is most frequent between the third and fifth decades of life in women and people of African-American ethnicity. Its origination is controversial, including the possible origins in muscle, fibroblasts, neural crest, neural sheath or histiocytes. The positivity for S-100 and CD68 suggest the neural origin.

O tumor de células granulares é uma neoplasia benigna rara, de origem neural. Relatamos caso de paciente feminina, 27 anos, com nódulo de superfície acastanhada no braço direito, cujo exame anatomopatológico evidenciou densa proliferação de células, com amplo citoplasma contendo grânulos eosinofílicos, e imuno-histoquímica positiva para proteínas S100 e CD68. O tumor de células granulares é geralmente solitário e, em metade dos casos, localiza-se em cabeça e pescoço, dos quais 23% na língua. É mais frequente entre a terceira e a quinta décadas de vida, em mulheres e pessoas de etnia negra. A positividade para S-100 e CD68 favorece origem neural.
Descritores: Neoplasias Cutâneas/patologia
Tumor de Células Granulares/patologia
-Imuno-Histoquímica
Antígenos de Diferenciação Mielomonocítica/metabolismo
Proteínas S100/metabolismo
Biomarcadores Tumorais/metabolismo
Antígenos CD/metabolismo
Limites: Humanos
Feminino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


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Id: biblio-827744
Autor: Gameiro, Ana; Gouveia, Miguel; Cardoso, José Carlos; Tellechea, Oscar.
Título: Histological variability and the importance of clinicopathological correlation in cutaneous Rosai-Dorfman disease
Fonte: An. bras. dermatol;91(5):634-637, Sept.-Oct. 2016. graf.
Idioma: en.
Resumo: Abstract: Rosai-Dorfman disease is a benign histiocytic proliferative disorder of unknown etiology. The disease mainly affects lymph node tissue, although it is rarely confined to the skin. Here, we describe a 53-year-old woman with purely cutaneous Rosai-Dorfman disease. The patient presented with a large pigmented plaque on her left leg, and sparse erythematous papules on her face and arms. A complete clinical response was achieved with thalidomide, followed by recurrence at the initial site one year later. The histological examination displayed the typical features of Rosai-Dorfman disease in the recent lesions but not in the older lesions. In the setting of no lymphadenopathy, the histopathological features of Rosai-Dorfman disease are commonly misinterpreted. Therefore, awareness of the histological aspects present at different stages, not always featuring the hallmark microscopic signs of Rosai-Dorfman disease, is particularly important for a correct diagnosis of this rare disorder.
Descritores: Dermatopatias/patologia
Histiocitose Sinusal/patologia
-Braço
Antígenos de Diferenciação Mielomonocítica/metabolismo
Proteínas S100/metabolismo
Antígenos CD/metabolismo
Diagnóstico Diferencial
Histiócitos/patologia
Perna (Membro)
Limites: Humanos
Feminino
Adolescente
Tipo de Publ: Relatos de Casos
Responsável: BR1.1 - BIREME


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Id: lil-797983
Autor: Vaz, Maysa Magalhães; Lopes, Lawrence Gonzaga; Cardoso, Paula Carvalho; Souza, João Batista de; Batista, Aline Carvalho; Costa, Nádia Lago; Torres, Érica Miranda; Estrela, Carlos.
Título: Inflammatory response of human dental pulp to at-home and in-office tooth bleaching
Fonte: J. appl. oral sci;24(5):509-517, Sept.-Oct. 2016. tab, graf.
Idioma: en.
Projeto: CAPES.
Resumo: ABSTRACT Tooth bleaching is a technique of choice to obtain a harmonious smile, but bleaching agents may damage the dental pulp. Objective: This study evaluated the inflammatory responses of human dental pulp after the use of two bleaching techniques. Material and Methods: Pulp samples were collected from human third molars extracted for orthodontic reasons and divided into three groups: control - no tooth bleaching (CG) (n=7); at-home bleaching with 15% carbamide peroxide (AH) (n = 10), and in-office bleaching with 38% hydrogen peroxide (IO) (n=12). Pulps were removed and stained with hematoxylin-eosin for microscopic analysis of inflammation intensity, collagen degradation, and pulp tissue organization. Immunohistochemistry was used to detect mast cells (tryptase+), blood vessels (CD31+), and macrophages (CD68+). Chi-square, Kruskal-Wallis, and Mann Whitney tests were used for statistical analysis. The level of significance was set at p<.05. Results: The inflammation intensity and the number of macrophages were significantly greater in IO than in AH and CG (p<0.05). The results of CD31+ (blood vessels per mm2) were similar in CG (61.39±20.03), AH (52.29±27.62), and IO (57.43±8.69) groups (p>0.05). No mast cells were found in the pulp samples analyzed. Conclusion: In-office bleaching with 38% hydrogen peroxide resulted in more intense inflammation, higher macrophages migration, and greater pulp damage then at-home bleaching with 15% carbamide peroxide, however, these bleaching techniques did not induce migration of mast cells and increased the number of blood vessels.
Descritores: Pulpite/induzido quimicamente
Clareamento Dental/efeitos adversos
Polpa Dentária/efeitos dos fármacos
Clareadores Dentários/toxicidade
-Peróxidos/toxicidade
Pulpite/patologia
Fatores de Tempo
Clareamento Dental/métodos
Ureia/análogos & derivados
Ureia/toxicidade
Vasos Sanguíneos/efeitos dos fármacos
Vasos Sanguíneos/patologia
Imuno-Histoquímica
Antígenos de Diferenciação Mielomonocítica
Distribuição Aleatória
Antígenos CD
Contagem de Células
Colágeno/efeitos dos fármacos
Estatísticas não Paramétricas
Molécula-1 de Adesão Celular Endotelial a Plaquetas
Polpa Dentária/patologia
Peróxido de Hidrogênio/toxicidade
Limites: Humanos
Tipo de Publ: Estudo de Avaliação
Responsável: BR1.1 - BIREME


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Id: biblio-975722
Autor: Özevren, Hüseyin; Irtegün, Sevgi; Ekingen, Arzu; Tuncer, Mehmet Cudi; Gökalp-Özkorkmaz, Ebru; Deveci, Engin; Deveci, Senay.
Título: Immunoexpression of vascular endothelial growth factor, beta-cell lymphoma 2 and cluster of differentiation 68 in cerebellar tissue of rats treated with Ganoderma lucidum / Inmunoexpresión del factor de crecimiento endotelial vascular, linfoma de células beta 2 y grupo de diferenciación 68 en tejido cerebeloso de ratas tratadas con Ganoderma lucidum
Fonte: Int. j. morphol;36(4):1453-1462, Dec. 2018. tab, graf.
Idioma: en.
Resumo: Traumatic brain injury (TBI) can potentially lead to hemorrhages in all areas of the skull, which can damage cells and nerve connections. This study aims to investigate the protective effects of Ganoderma lucidum polysaccharides (GLPS) as a antioxidant on cerebellar cell tissues after traumatic brain injury in rats. Sprague Dawley rats were subjected to TBI with a weight-drop device using 300 g1m weight-height impact. The groups are consisted of control, trauma, and trauma+Ganoderma lucidum groups. At seven days post-brain injury, experimental rats were decapitated after intraperitoneal administration of ketamine HCL (0.15 ml/100 g body weight). Cereballar samples were taken for histological examination or determination of malondialdehyde (MDA) and glutathione (GSH) levels and myeloperoxidase (MPO) activity. Significant improvement was observed in cells and vascular structures of Ganoderma lucidum treated groups when compared to untreated groups. It is believed that Ganoderma lucidum may have an effect on the progression of traumatic brain injury. Ganoderma lucidum application may affect angiogenetic development in blood vessel endothelial cells, decrease inflammatory cell accumulation by affecting cytokine mechanism and may create apoptotic nerve cells and neuroprotective mechanism in glial cells.

La lesión cerebral traumática (LCT) puede provocar hemorragias en todas las áreas del cráneo, lo que puede dañar las células y las conexiones nerviosas. Este estudio tuvo como objetivo investigar los efectos protectores de los polisacáridos de Ganoderma lucidum (GLPS) como antioxidante en los tejidos de las células del cerebelo después de la lesión cerebral traumática en ratas. Ratas Sprague Dawley fueron sometidas a TBI con un dispositivo de caída de peso usando un impacto de peso de 300 g-1 m. Se formaron los siguientes grupos: control, trauma y trauma + Ganoderma lucidum. Siete días después de la lesión cerebral, las ratas experimentales fueron decapitadas después de la administración intraperitoneal de ketamina HCL (0,15 ml / 100 g de peso corporal). Se tomaron muestras cerebrales para el examen histológico y para la determinación de niveles de malondialdehído (MDA) y glutatión (GSH) y actividad de mieloperoxidasa (MPO). Se observó una mejora significativa en las células y las estructuras vasculares de los grupos tratados con Ganoderma lucidum en comparación con los grupos no tratados. Durante el estudio se observó que Ganoderma lucidum puede tener un efecto sobre la progresión de la lesión cerebral traumática. La aplicación de Ganoderma lucidum puede afectar el desarrollo angiogénico en las células endoteliales de los vasos sanguíneos, disminuir la acumulación de células inflamatorias al afectar el mecanismo de las citocinas y puede crear células nerviosas apoptóticas y un mecanismo neuroprotector en las células gliales.
Descritores: Cerebelo/efeitos dos fármacos
Reishi/química
Lesões Encefálicas Traumáticas/patologia
Antioxidantes/farmacologia
-Polissacarídeos/farmacologia
Imuno-Histoquímica
Antígenos de Diferenciação Mielomonocítica
Antígenos CD
Cerebelo/metabolismo
Cerebelo/patologia
Western Blotting
Ratos Sprague-Dawley
Peroxidase/metabolismo
Fármacos Neuroprotetores
Proteínas Proto-Oncogênicas c-bcl-2
Fator A de Crescimento do Endotélio Vascular/metabolismo
Glutationa/análise
Malondialdeído/análise
Limites: Animais
Masculino
Ratos
Responsável: CL1.1 - Biblioteca Central


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Id: lil-766982
Autor: Gianelo, M.C.S.; Polizzelo, J.C.; Chesca, D.; Mattiello-Sverzut, A.C..
Título: Three days of intermittent stretching after muscle disuse alters the proteins involved in force transmission in muscle fibers in weanling rats
Fonte: Braz. j. med. biol. res = Rev. bras. pesqui. méd. biol;49(2):e4118, 2016. tab, graf.
Idioma: en.
Resumo: The aim of this study was to determine the effects of intermittent passive manual stretching on various proteins involved in force transmission in skeletal muscle. Female Wistar weanling rats were randomly assigned to 5 groups: 2 control groups containing 21- and 30-day-old rats that received neither immobilization nor stretching, and 3 test groups that received 1) passive stretching over 3 days, 2) immobilization for 7 days and then passive stretching over 3 days, or 3) immobilization for 7 days. Maximal plantar flexion in the right hind limb was imposed, and the stretching protocol of 10 repetitions of 30 s stretches was applied. The soleus muscles were harvested and processed for HE and picrosirius staining; immunohistochemical analysis of collagen types I, III, IV, desmin, and vimentin; and immunofluorescence labeling of dystrophin and CD68. The numbers of desmin- and vimentin-positive cells were significantly decreased compared with those in the control following immobilization, regardless of whether stretching was applied (P<0.05). In addition, the semi-quantitative analysis showed that collagen type I was increased and type IV was decreased in the immobilized animals, regardless of whether the stretching protocol was applied. In conclusion, the largest changes in response to stretching were observed in muscles that had been previously immobilized, and the stretching protocol applied here did not mitigate the immobilization-induced muscle changes. Muscle disuse adversely affected several proteins involved in the transmission of forces between the intracellular and extracellular compartments. Thus, the 3-day rehabilitation period tested here did not provide sufficient time for the muscles to recover from the disuse maladaptations in animals undergoing postnatal development.
Descritores: Imobilização/fisiologia
Exercícios de Alongamento Muscular
Fibras Musculares Esqueléticas/metabolismo
Proteínas Musculares/metabolismo
Força Muscular/fisiologia
-Antígenos CD/análise
Antígenos de Diferenciação Mielomonocítica/análise
Colágeno Tipo I/análise
Colágeno Tipo I/metabolismo
Colágeno Tipo III/análise
Colágeno Tipo III/metabolismo
Colágeno Tipo IV/análise
Colágeno Tipo IV/metabolismo
Desmina/análise
Desmina/metabolismo
Distrofina/análise
Imunofluorescência
Corpos de Inclusão/metabolismo
Distribuição Aleatória
Ratos Wistar
Fatores de Tempo
Vimentina/análise
Vimentina/metabolismo
Limites: Animais
Feminino
Tipo de Publ: Research Support, Non-U.S. Gov't
Responsável: BR1.1 - BIREME


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Id: lil-755504
Autor: Yavuz, D; Balsak, D; Ekinci, C; Tahaoglu, A. E; Togrul, C; Görük, N; Aktas, A; Karaman, E.
Título: Expression of VEGF and CD68 in the placenta of gestational diabetic mothers (immunohistochemistry and ultrastructural study) / Expresión de VEGF y CD68 en la placenta de madres diabéticas gestacionales (estudio inmunohistoquímico y ultraestructural)
Fonte: Int. j. morphol;33(2):522-526, jun. 2015. ilus.
Idioma: en.
Resumo: Placental angiogenesis, is essential for embryonic and fetal development. In this study, 18 gestational diabetes mellitus and 22 control pregnancies were included. Gestational diabetes mellitus (GDM) groups compared to the control group significantly higher values were detected (p<0.01). The following histological results were assessed; villous immaturity, chorangiosis, presence of, sncytial knots,mononuclear cell infiltration ischemia and fibrinoid necrosis. To evaluate and compare the placental histology of normal and GDM pregnancies. placentas of pregnant women with gestational diabetes also in terms of angiogenesis and macrophages and ultratructural revealed by examining the possible relationship between fetal complications were investigated.

La angiogénesis de la placenta es esencial para el desarrollo embrionario y fetal. En este estudio, se incluyeron 18 casos de diabetes mellitus gestacional (DMG) y 22 embarazos de control. En grupos los de DMG en comparación con el control, se detectaron valores significativamente mayores (p<0,01) en los siguientes parámetros histológicos que fueron evaluados: inmadurez vellosa, chorangiosis, presencia de nodos sincicial, infiltración celular isquémica mononuclear y necrosis fibrinoide. La investigación de las placentas de mujeres con DMG, reveló mediante el examen en términos de angiogénesis, macrófagos y ultraestructural, la posible relación entre las complicaciones fetales.
Descritores: Antígenos CD/metabolismo
Diabetes Gestacional/metabolismo
Diabetes Gestacional/patologia
Placenta/ultraestrutura
Fator A de Crescimento do Endotélio Vascular/metabolismo
-Antígenos de Diferenciação Mielomonocítica
Imuno-Histoquímica
Microscopia Eletrônica
Placenta/metabolismo
Limites: Humanos
Feminino
Gravidez
Responsável: CL1.1 - Biblioteca Central


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Id: lil-718407
Autor: Lopes, Germison Silva; Leitão, João Paulo de Vasconcelos; Kaufman, Jacques; Duarte, Fernando Barroso; Matos, Daniel Mazza.
Título: T-cell/myeloid mixed-phenotype acute leukemia with monocytic differentiation and isolated 17p deletion
Fonte: Rev. bras. hematol. hemoter;36(4):293-296, Jul-Aug/2014. graf.
Idioma: en.
Resumo: Mixed phenotype acute leukemia is a rare subtype of leukemia that probably arises from a hematopoietic pluripotent stem cell. The co-expression of two of myeloid, B- or T-lymphoid antigens is the hallmark of this disease. Herein, the case of a 28-year-old female patient is reported who presented with hemoglobin of 5.8 g/dL, white blood cell count of 138 × 109/L and platelet count of 12 × 109/L. The differential count of peripheral blood revealed 96% of blasts. Moreover, the patient presented with lymphadenopathy, splenomegaly and bone marrow infiltration by monocytoid blasts characterized as 7% positivity by Sudan Black cytochemical staining. Immunophenotyping revealed the involvement of blasts of both T- and monocytic lineages. The cytogenetic analysis showed an isolated 17p deletion. Thus, the diagnosis of T-cell/myeloid mixed phenotype acute leukemia was made with two particular rare features, that is, the monocytic differentiation and the 17p deletion as unique cytogenetic abnormalities. The possibility of concomitant expressions of T-cell and monocytic differentiation antigens in the same blast population is hard to explain using the classical model of hematopoiesis. However, recent studies have suggested that myeloid potential persists even when the lineage branches segregate toward B- and T-cells. The role of an isolated 17p deletion in the pathogenesis of this condition is unclear. At present, the patient is in complete remission after an allogeneic stem cell transplantation procedure...
Descritores: Antígenos
Antígenos de Diferenciação Mielomonocítica
Deleção Cromossômica
CROMOSSOMOS HUMANOS PAR ABNORMALITIES, RADIATION-INDUCED
Citometria de Fluxo
Leucemia Aguda Bifenotípica
Leucemia Monocítica Aguda
Leucemia Mieloide Aguda
Limites: Humanos
Feminino
Adulto
Tipo de Publ: Relatos de Casos
Responsável: BR408.1 - Biblioteca da Faculdade de Medicina - BFM


  8 / 14 LILACS  
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Id: lil-681863
Autor: Brazilian Dental Journal; Boas, Deise Souza Vilas; Takiya, Christina Maeda; Gurgel, Clarissa Araujo Silva; Cabral, Marcia Grillo; Santos, Jean Nunes dos.
Título: Tumor-Infiltrating Macrophage and Microvessel Density in Oral Squamous Cell Carcinoma
Fonte: Braz. dent. j;24(3):194-199, May-Jun/2013. tab, graf.
Idioma: en.
Resumo: Tumor-associated macrophages (TAM) are the main cellular component in stroma of many tumors and participate in tumor angiogenesis. The aim of present study was to compare the microvascular density (MVD) and infiltrating macrophage density (IMD) in oral squamous cell carcinomas (OSCCs) with different histological grades. A histomorphometric analysis was performed after immunohistochemistry using antibodies such as von-Willebrand factor and CD68. A significant difference in MVD was found between well and moderately differentiated OSCCs (p<0.05). TAM were largely present in all studied tumors and the IMD was not different among OSCCs with different histological grades (p=0.381). Significant correlation between MVD and IMD was not observed (p=0.870). In conclusion, these results suggest that TAM and angiogenesis have an influence at different histological grades of OSCC. However, the lack of correlation between MVD and IMD could suggest that angiogenesis does not depend on the number of macrophages present in OSCC, but their predominant phenotype. Further studies involving distinct phenotypes of macrophages should be done to better understand the influence of TAM on the tumor angiogenesis.

Macrófagos associados a tumores (MAT) representam o componente principal do estroma de muitos tumores, além de participar da angiogênese tumoral. Este estudo comparou a microdensidade vascular (MDV) e densidade de macrófagos infiltrando o tumor (DMIT) em carcinoma escamocelular da boca (CEC) com diferentes graus histológicos de malignidade. Análise histomorfométrica foi empregada após técnica imuno-histoquímica para os anticorpos fator von-Willebrand e CD68. Uma diferença significante entre MDV e carcinomas bem e moderadamente diferenciados foi observada (p<0,05). MAT estavam fortemente presentes em todos os tumores estudados e a DMIT não foi diferente entre os diferentes graus histológicos de malignidade do CEC (p=0,381). Correlação significante entre MDV e DMIT não foi observada (p=0,870). Em conclusão, os resultados desse estudo sugerem a influência de MAT e angiogênese nos diferentes graus histológicos de malignidade do CEC. Entretanto, a ausência de correlação entre MDV e DMIT sugere que a angiogênese não depende do número de macrófagos presentes neste tipo de câncer, mas do fenótipo predominante. Outros estudos devem ser realizados a fim de contribuir para melhor compreensão da participação de MAT na angiogênese tumoral.
Descritores: Carcinoma de Células Escamosas/patologia
Macrófagos/patologia
Microvasos/patologia
Neoplasias Bucais/patologia
-Antígenos CD/análise
Antígenos de Diferenciação Mielomonocítica/análise
Contagem de Células
Carcinoma de Células Escamosas/irrigação sanguínea
Células Endoteliais/patologia
Endotélio Vascular/patologia
Neoplasias Gengivais/irrigação sanguínea
Neoplasias Gengivais/patologia
Imuno-Histoquímica
Soalho Bucal/irrigação sanguínea
Soalho Bucal/patologia
Neoplasias Bucais/irrigação sanguínea
Gradação de Tumores
Neovascularização Patológica/patologia
Fenótipo
Neoplasias da Língua/irrigação sanguínea
Neoplasias da Língua/patologia
Fator de von Willebrand/análise
Limites: Feminino
Humanos
Masculino
Pessoa de Meia-Idade
Tipo de Publ: Estudo Comparativo
Research Support, Non-U.S. Gov't
Responsável: BR1.1 - BIREME


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Id: lil-666038
Autor: Mendes, Dayana Santos; Dantas, Marina Loyola; Gomes, Juliana Menezes; Santos, Washington Luis Conrado dos; Silva, Adriano Queiroz; Guimarães, Luiz Henrique; Machado, Paulo R; Carvalho, Edgar Marcelino de; Arruda, Sérgio.
Título: Inflammation in disseminated lesions: an analysis of CD4+, CD20+, CD68+, CD31+ and vW+ cells in non-ulcerated lesions of disseminated leishmaniasis
Fonte: Mem. Inst. Oswaldo Cruz;108(1):18-22, Feb. 2013. ilus, graf, tab.
Idioma: en.
Projeto: NIH.
Resumo: Disseminated leishmaniasis (DL) differs from other clinical forms of the disease due to the presence of many non-ulcerated lesions (papules and nodules) in non-contiguous areas of the body. We describe the histopathology of DL non-ulcerated lesions and the presence of CD4-, CD20-, CD68-, CD31- and von Willebrand factor (vW)-positive cells in the inflamed area. We analysed eighteen biopsies from non-ulcerated lesions and quantified the inflamed areas and the expression of CD4, CD20, CD68, CD31 and vW using Image-Pro software (Media Cybernetics). Diffuse lymphoplasmacytic perivascular infiltrates were found in dermal skin. Inflammation was observed in 3-73% of the total biopsy area and showed a significant linear correlation with the number of vW+ vessels. The most common cells were CD68+ macrophages, CD20+ B-cells and CD4+ T-cells. A significant linear correlation between CD4+ and CD20+ cells and the size of the inflamed area was also found. Our findings show chronic inflammation in all DL non-ulcerated lesions predominantly formed by macrophages, plasmacytes and T and B-cells. As the inflamed area expanded, the number of granulomas and extent of the vascular framework increased. Thus, we demonstrate that vessels may have an important role in the clinical evolution of DL lesions.
Descritores: Inflamação/imunologia
Leishmaniose Cutânea/imunologia
-Antígenos CD/imunologia
/imunologia
ANTIGENS, CDABOMASUM/imunologia
Antígenos de Diferenciação Mielomonocítica/imunologia
Linfócitos B/imunologia
Linfócitos B/patologia
Biópsia
/imunologia
CDABBREVIATIONS AS TOPIC-POSITIVE T-LYMPHOCYTES/imunologia
Doença Crônica
Progressão da Doença
Inflamação/patologia
Leishmaniose Cutânea/patologia
Macrófagos/imunologia
Macrófagos/patologia
Fator de von Willebrand/imunologia
Limites: Adolescente
Adulto
Criança
Pré-Escolar
Feminino
Humanos
Masculino
Pessoa de Meia-Idade
Adulto Jovem
Tipo de Publ: Research Support, N.I.H., Extramural
Responsável: BR1.1 - BIREME


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Id: lil-633900
Autor: Alvarez, Clarisa L.; Dorado, Enrique; Sarano, Judith F..
Título: Nefropatía crioglobulinémica CD 68 positivo en monocitos/macrófagos glomerulares
Fonte: Medicina (B.Aires);71(5):465-465, oct. 2011. ilus.
Idioma: es.
Descritores: Antígenos CD/análise
Antígenos de Diferenciação Mielomonocítica/análise
Crioglobulinemia/patologia
Glomerulonefrite/patologia
-Crioglobulinemia/imunologia
Glomerulonefrite/imunologia
Imunoglobulinas/análise
Glomérulos Renais/patologia
Macrófagos/patologia
Monócitos/patologia
Limites: Adulto
Feminino
Humanos
Tipo de Publ: Relatos de Casos
Responsável: AR1.2 - Instituto de Investigaciónes Epidemiológicas



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