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1.
J. appl. oral sci ; 25(3): 318-323, May-June 2017. tab, graf
Artigo em Inglês | LILACS, BBO, BNUY, BNUY-Odon | ID: biblio-893624

RESUMO

Abstract Objectives To evaluate the number of AgNORs per nucleus and the expression of Ki-67 at the tumor invasion front (TIF) in relation to clinical parameters (TNM), TIF classification and the prognosis of oral squamous cell carcinomas in an Uruguayan population. Material and Methods This study was conducted through a retrospective survey from 2000 to 2010 at the National Institute of Cancer Montevideo, Uruguay and included 40 patients. The samples were obtained from the resection of the tumor and the TIF was defined according with Bryne, et al.5 (1992). Expression of Ki-67 was assessed by the percentage of positive tumor cells and the AgNOR was recorded as the mean AgNOR (mAgNOR) and the percentage of AgNOR per nucleus (pAgNOR). All analyzes were performed by a blinded and calibrated observer. Results No statistically significant association was observed between immunostaining of Ki-67 and AgNOR with the different types of TIF, regional metastasis and patients prognosis, however it was observed an increase in Ki-67 expression associated with worse patient's clinical staging, although not statistically significant. Conclusions Our results suggest that proliferation markers as AgNOR and Ki-67 are not prognostic markers at the tumor invasive front of carcinoma of oral squamous cell.


Assuntos
Humanos , Masculino , Feminino , Adulto , Pessoa de Meia-Idade , Idoso , Idoso de 80 Anos ou mais , Neoplasias Bucais/patologia , Carcinoma de Células Escamosas/patologia , Antígenos Nucleares/análise , Prognóstico , Valores de Referência , Uruguai , Imuno-Histoquímica , Biomarcadores Tumorais , Reprodutibilidade dos Testes , Estudos Retrospectivos , Análise de Variância , Antígeno Ki-67/análise , Carga Tumoral , Proliferação de Células , Invasividade Neoplásica/patologia
2.
Colomb. med ; 47(2): 87-93, Apr.June 2016. ilus
Artigo em Inglês | LILACS | ID: lil-791144

RESUMO

Objective: To evaluate transcallosal changes after a local ischemic injury in rats by using the monoclonal marker anti-NeuN (Mouse anti-neuronal nuclei). Methods: Twenty eight adult, male, Wistar rats were subjected to focal injury in the right hemisphere. The technique used was the experimental model of focal ischemic injury through intraluminal suture of the middle cerebral artery. Analyses were made for the five groups: and after the lesion (control), at 24 h, 96 h, 10 days and 20 days. Exofocal neuronal damage was inferred from neuronal immunoreactivity changes to NeuN. Results: In the cortex contralateral to the lesion, immunoreactivity was diminished. This was most notable in the supragranular layers 24 h post ischemia. After 96 h, there was a generalized diminishment of the inmmunoreactivity in supra and infragranular layers. At 10 and 20 days, the tissue recovered some NeuN immunoreactivity, but there were set changes in the VI layer. Conclusion: The immunoreactive changes to NeuN support the process of interhemispheric diaschisis. Changes in immunoreactivity could indicate metabolic stress secondary to the disruption in connectivity to the site of lesion.


Objetivo: Evaluar los cambios exofocales transcallosos después de lesión isquémica focal en ratas, mediante marcación inmunohistoquímica con el anticuerpo monoclonal anti-NeuN (Mouse Anti-Neuronal Nuclei). Métodos: Se intervinieron 28 ratas machos Wistar adultas. Mediante el modelo experimental de isquemia cerebral focal del territorio de la arteria cerebral media por filamento intraluminal, se les ocasionó una lesión focal en el hemisferio derecho. Posteriormente se evaluó el hemisferio contralateral, marcando la población neuronal con el anticuerpo monoclonal anti-NeuN. Se definieron cinco grupos de evaluación: uno de control, 24 h, 96 h, 10 días y 20 días. Se evaluaron los cambios neuronales exofocales después de la lesión con base en la observación de los cambios en la inmunoreactividad de las neuronas al NeuN. Resultados: Se redujo la inmunoreactividad en la corteza contralateral a la lesión. Este fenómeno fue más notable en las capas supragranulares después de 24 h post isquemia. Después de 96 h hubo una disminución generalizada de la inmmunoreactivity en las capas supra e infragranulares. A los 10 y 20 días, el tejido recobró alguna inmunoreactividad NeuN, estos cambios se dieron en la capa VI. Conclusiones: Los cambios inmunorreactivos a NeuN apoyan el proceso de diasquisis interhemisférica. Los cambios en la inmunorreactividad podrían indicar estrés metabólico secundario a la interrupción en la conectividad con el sitio de la lesión.


Assuntos
Animais , Masculino , Ratos , Isquemia Encefálica/complicações , Corpo Caloso/patologia , Artéria Cerebral Média , Antígenos Nucleares/análise , Imuno-Histoquímica , Biomarcadores , Isquemia Encefálica/patologia , Ratos Wistar , Corpo Caloso/imunologia , Antígenos Nucleares/imunologia , Anticorpos Monoclonais , Necrose
3.
Artigo em Inglês | IMSEAR | ID: sea-51859

RESUMO

BACKGROUND AND OBJECTIVE: Argyrophilic nucleolar organizer regions (AgNORs) have found widespread application in the past, especially in tumor histopathology. This study was undertaken to evaluate the significance of various AgNOR parameters and to assess their role in differentiating hyperplastic, premalignant, and malignant lesions. MATERIALS AND METHODS: The study sample consisted of archival biopsy specimens of ten squamous cell carcinomas, ten premalignant lesions, and five inflammatory lesions. Two biopsies from normal mucosa acted as control. AgNORs were assessed both quantitatively and qualitatively. The data were analyzed using Student's independent t-test, one-way analysis of variance (ANOVA), and multiple range test (Tukey-HSD). RESULTS: Quantitatively significant difference existed in the number of AgNORs between the normal mucosa, inflammatory lesions, and carcinomas, but the premalignant lesions failed to differ significantly from the normal mucosa. The number of AgNORs was found to be related to epithelial proliferation. Qualitatively, in terms of size, shape, and pattern of distribution, the normal mucosa and inflammatory lesion were alike, but the premalignant and malignant lesions differed significantly from the normal, with a marked degree of AgNOR pleomorphism being observed in carcinomas. CONCLUSIONS: AgNOR quantity is strictly proportional to the proliferative activity of the cell and does not necessarily indicate malignancy. It is the qualitative characteristics of AgNOR that help to differentiate hyperplastic, premalignant, and malignant lesions.


Assuntos
Antígenos Nucleares/análise , Carcinoma de Células Escamosas/química , Proliferação de Células , Diagnóstico Diferencial , Granuloma Piogênico/patologia , Humanos , Leucoplasia Oral/química , Doenças da Boca/patologia , Mucosa Bucal/química , Neoplasias Bucais/química , Região Organizadora do Nucléolo/patologia , Lesões Pré-Cancerosas/química , Coloração pela Prata , Biomarcadores Tumorais
4.
Indian J Pathol Microbiol ; 2008 Jan-Mar; 51(1): 97-101
Artigo em Inglês | IMSEAR | ID: sea-73748

RESUMO

Thirty-five adult myelodysplastic syndrome (MDS) patients were included in this study: 11 refractory anemia (RA), 4 RA with ring sideroblasts (RARS), 9 RA with excess of blasts (RAEB), 10 RAEB in transformation (RAEB-T) and 1 chronic myelomonocytic leukemia (CMML). The ranges of survival were 4-51 months, 40-59 months, 7-38 months, 5-24 months and 5 days, respectively. Three patients died and 3 showed disease progression during the course of the study. A composite analysis of proliferative indices, cytogenetics, immunophenotype and other conventional/novel prognostic parameters in the context of Indian MDS patients was performed. The proliferative indices (AgNOR and Ki 67 positivity), immunophenotypic markers, serum LDH and ferritin levels revealed wide variations and great overlap among different FAB subtypes. The scoring systems (Bournemouth, Dusseldorf and Goasguen) did not correlate with the prognosis and survival (p > 0.05). Clonal cytogenetic abnormalities were detected in 24/35 (68.57%) patients, +8, -5 and -7 being observed commonly. Cytogenetic abnormalities were more frequent in RAEB (88.8%), RAEB-T (80.0%) and RA (63.6%) subtypes of MDS. By Using Mufti's prognostic system and International prognostic scoring system (IPSS), a good positive correlation was found between low risk category and RARS with better survival as compared to other risk categories/FAB subtypes (p < 0.01). However, rest of the FAB subtypes were assigned into high, intermediate and low risk categories without any correlation with the survival and/or leukemic transformation. RARS subtype revealed itself as the better prognostic category according to the cytogenetic findings as well as Mufti's grading system. This was possible due to the longer follow up available for these patients (40-59 months).


Assuntos
Adolescente , Adulto , Idoso , Idoso de 80 Anos ou mais , Antígenos Nucleares/análise , Biomarcadores , Células Sanguíneas/química , Medula Óssea/química , Progressão da Doença , Feminino , Ferritinas/sangue , Humanos , Antígeno Ki-67/análise , L-Lactato Desidrogenase/sangue , Masculino , Pessoa de Meia-Idade , Síndromes Mielodisplásicas/diagnóstico , Prognóstico , Índice de Gravidade de Doença , Análise de Sobrevida
5.
Acta odontol. latinoam ; 20(1): 55-60, 2007. ilus, tab
Artigo em Inglês | LILACS | ID: lil-483934

RESUMO

Maxillary osteosarcomas are a relatively frequent malignant tumor of the oral cavity. Similarly to other skeletal osteosarcomas, they exhibit different cellular differentiation patterns, i.e. chondroblastic, osteoblastic, or fibroblastic. Although their histological features resemble those of osteosarcomas of the long bones, their pattern of evolution usually differs. Morphometric variations in silver stained Nucleolar Organizer Regions (AgNOR) have proved of value to study the biology of several tumors. However, information on the analysis of AgNOR in maxillary tumors is scarce. The aim of the present study was to analyze the variations of different morphological parameters related to AgNOR in a series of 32 cases of maxillary osteosarcoma. In each case we analyzed 100 nuclei corresponding to the prevalent cellular differentiation type, selecting the most aggressive area. We employed software previously developed at our laboratory that yields information on different AgNOR-related parameters. The results were compared with those previously reported in a study on 12 cases of osteosarcoma of long bones. Six cases of oral mucosa squamous cell carcinoma were also included for comparative purposes. Single AgNOR volume proved to be the most discriminatory and informative parameter. The value of single AgNOR volume was considerably lower in mandible osteosarcomas than in osteosarcomas of the upper maxilla (p=0.02). The values were significantly lower in maxillary osteosarcomas than in long bone osteosarcomas and in oral carcinomas. This finding would suggest a slower rate of cell activity in maxillary osteosarcomas, associated in turn to its known lower degree of aggressiveness. The present results suggest that the analysis of AgNOR is a valuable and easily applicable marker to determine the degree of malignancy and biology of maxillary osteosarcomas.


Los osteoscaromas de maxilares son entidades relativamente frecuentes entre los tumores malignos de la cavidad bucal. Al igual que los osteosarcomas de otras localizaciones del esqueleto, pueden presentar diferentes patrones de diferenciación celular (condroblástico, osteoblástico o fibroblástico). Si bien sus características histológicas son similares, tienen generalmente un comportamiento evolutivo diferente al de los huesos largos. Las variaciones morfométricas de las regiones organizadoras del nucleoloidentificadas por impregnación argéntica (AgNOR) han demostrado ser marcadores útiles para el estudio de la biología de diversas entidades tumorales, pero hay muy escasa información de su análisis en tumores de los huesos maxilares. El objetivo de este trabajo fue analizar las variaciones de diferentes parámetros morfológicos de las AgNOR en una serie de 32 casos de osteosarcomas de maxilar. En cada caso se analizaron 100 núcleos en el patrón de diferenciación celular predominante, seleccionando la zona de mayor agresividad. Se utilizó un programa que aporta información sobre diferentes parámetros de AgNOR, desarrollado previamente en nuestro laboratorio. El parámetro más indicativo resultó ser el volumen individual de las AgNOR. Este parámetro en los osteosarcomas con localización mandibular fue considerablemente menor que aquellos localizados en maxilar superior (p=0.02). En los osteosarcomas de maxilar los valores fueron significativamente menores que en los de huesos largos y en los carcinomas bucales. Ellos podría ser indicativo de una menor actividad celular, a su vez asociada a su reconocida menor agresividad. Estos resultados sugieren que el análisis de AgNOR podría ser considerado como un marcador de utilidad y de fácil aplicación para determinar el grado de malignidad en osteosarcomas de maxilar y estimar su comportamiento biológico.


Assuntos
Humanos , Biomarcadores Tumorais , Neoplasias Maxilares/patologia , Osteossarcoma , Região Organizadora do Nucléolo/patologia , Análise de Variância , Antígenos Nucleares/análise , Carcinoma de Células Escamosas/patologia , Invasividade Neoplásica , Proteínas Nucleares/análise , Coloração pela Prata
6.
Indian J Pathol Microbiol ; 2006 Jan; 49(1): 17-20
Artigo em Inglês | IMSEAR | ID: sea-73154

RESUMO

AgNOR staining was employed on FNAC and histopathological sections obtained from patients with soft tissue tumours. The study comprised of 20 normal appearing soft tissues, 74 benign and 36 malignant soft tissue tumours. The slides were stained with AgNOR in order to differentiate between benign and malignant soft tissue tumours. The mean AgNOR count in normal appearing soft tissues, benign lesions and malignant lesions was 1.04+/-0.10 (0.94-1.14), 1.51+/-0.21 (1.1-2.1) and 4.96+/-1.33 (2.57-7.21) respectively. The mean AgNOR count was found to be higher in benign soft tissue tumours as compared to normal appearing soft tissues and the difference was found to be statistically significant. The mean AgNOR count in soft tissue sarcomas was found to be higher as compared to both normal appearing soft tissues and benign soft tissue tumours and the results were found to be statistically significant. The increased AgNOR score in both benign and malignant soft tissue tumours as compared to normal appearing soft tissues indicates high proliferative activity. Thus AgNOR staining is a simple and useful method for estimating tumour cell proliferation thereby differentiating normal appearing soft tissues from benign and malignant soft tissue tumours.


Assuntos
Adolescente , Adulto , Idoso , Antígenos Nucleares/análise , Biópsia , Proliferação de Células , Criança , Histocitoquímica/métodos , Humanos , Pessoa de Meia-Idade , Proteínas Nucleares/análise , Coloração pela Prata/métodos , Neoplasias de Tecidos Moles/química
7.
Indian J Pathol Microbiol ; 2004 Jul; 47(3): 354-8
Artigo em Inglês | IMSEAR | ID: sea-73807

RESUMO

Prostatic lesions on routine H&E stain sometimes cause diagnostic dilemma specially in premalignant lesions like A.A.H. and P.I.N. Proliferative markers (AgNOR, P.C.N.A) are of great help in this grey zone. Total 50 cases studied and provisional diagnosis after HIE stain revealed that 37 cases were B.H.P., 5 cases were A.A.H., 1 case was P.I.N and 7 cases were adenocarcinoma. Proliferative marker study revealed AgNOR count of B.H.P as (0.4 -2.5)/cell, of A.A.H as (1.5-3.2)/cell, of P.I.N as 4.8/cell and adenocarcinoma as (4.3-5.4)/cell. P.C.N.A index of B.H.P was (2-8)%, of A.A.H (17-35)%, of P.I.N 40% and of carcinoma (54-82)%. Proliferative marker study was of great help in distinguishing between benign and malignant and specially premalignant lesions like A.A.H and P.I.N, where routine histopathology diagnosis was confusing. In the study, P.C.N.A was found to be superior to AgNOR since the values for interpretation was wider.


Assuntos
Adenocarcinoma/patologia , Idoso , Antígenos Nucleares/análise , Biomarcadores/análise , Divisão Celular , Humanos , Masculino , Pessoa de Meia-Idade , Índice Mitótico , Proteínas Nucleares/análise , Antígeno Nuclear de Célula em Proliferação/análise , Hiperplasia Prostática/patologia , Neoplasias da Próstata/patologia
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