Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 10 de 10
Filtrar
Mais filtros










Base de dados
Intervalo de ano de publicação
1.
J Med Life ; 10(1): 85-89, 2017.
Artigo em Inglês | MEDLINE | ID: mdl-28255385

RESUMO

Reelin is an extracellular signaling protein synthesized by Cajal-Retius cells in utero and early after birth, its presence being signaled in adult life too. Reelin acts on its receptors, VLDLR and ApoER2, acting on cytoskeleton, controlling migration and subsequently positioning and stabilizing the cortical neurons. We investigated the reelin presence and its receptors, VLDLR and ApoER2, in melanocytic nevi considering the neural crest origin of the nevus cells and their migration into skin during embrionary period. Melanocytic nevi present a strict cellular architecture and an increased malignant transforming capacity. We investigated reelin presence in 32 melanocytic nevi (5 junctional, 27 compound or 14 dysplastic nevi and 18 non dysplastic nevi). The assessment of reelin presence was performed by histological semiquantitative criteria. Results showed the presence of reelin in 29 cases (29/ 32). The presence of reelin was elevated in junctional areas as in dysplastic nevi. VLDLR presented positive values in 16 cases (16/ 32) and ApoER2 was weak positive in 7 cases. Reelin or its receptors was peritumorally absent. Our study showed the presence of reelin in nevus cells from cutaneous melanocytic nevi and, in these cells, only the VLDLR receptor was present in half of the cases. The significance of the reelin presence in cutaneous nevus cells may be hypothetically considered correlated with the position maintenance of the nevus cells or migration of these cells in malignant transforming situation. Abbreviations: ApoER2 = apolipoprotein receptor 2, VLDLR = very low density lipoprotein receptor, DAB-1 = DIABLO protein, HMB45 = gene HMB45.


Assuntos
Moléculas de Adesão Celular Neuronais/metabolismo , Proteínas da Matriz Extracelular/metabolismo , Proteínas Relacionadas a Receptor de LDL/metabolismo , Proteínas do Tecido Nervoso/metabolismo , Nevo Pigmentado/metabolismo , Receptores de LDL/metabolismo , Serina Endopeptidases/metabolismo , Adolescente , Adulto , Animais , Feminino , Humanos , Imuno-Histoquímica , Masculino , Pessoa de Meia-Idade , Nevo Pigmentado/patologia , Proteína Reelina , Adulto Jovem
3.
Chirurgia (Bucur) ; 110(2): 144-50, 2015.
Artigo em Inglês | MEDLINE | ID: mdl-26011836

RESUMO

INTRODUCTION: The paper deals with the diagnosis of some aggressive forms of uterine cervix cancers, resistant to radio chemotherapy, using biomolecular markers.For this study, the destruction of tumours in stages II-IIIBis carried out by hyperthermia induced by different sources of energy. The aimed targets are toembed a quick and simple technique of haemostas isused in bleeding uterine cervix tumours associated with acute an aemiain the treatment protocols and to identify biomolecular criteria revealing tumour aggressiveness and treatment response. METHOD: The proposed method consists in radio frequency ablation (RFA) applied touterine cervix bleeding tumours with acute secondary anaemia. Studying 16 patients displaying aggressive cancer forms resistant to radio chemotherapy treated by the above mentioned method, we assessed that the commonly present markers: Ki67, p53 and Bcl-2, may be a substantial indication of such cases. Aggressiveness and treatment resistance was defined based on clinical and paraclinical investigations. RESULTS: RFA haemostasis achieved in approximately 20 m inproved the efficiency of this method. A secondary important effect was local tumour volume decrease, resulting in the improvement of radio-chemotherapy responsiveness. CONCLUSIONS: Once an aggressive and radio-chemotherapy resistant cancer is diagnosed,the quantitative, qualitative and associative presence of the biomolecular markers mentioned herein before, could influence the personalised treatment attitude (radiofrequency, neoadjuvant chemotherapy), which onthe long term, may increase patient survival and life quality improvement.


Assuntos
Biomarcadores Tumorais/sangue , Carcinoma de Células Escamosas/diagnóstico , Ablação por Cateter , Genes bcl-2 , Antígeno Ki-67/sangue , Proteína Supressora de Tumor p53/sangue , Neoplasias do Colo do Útero/diagnóstico , Adulto , Idoso , Carcinoma de Células Escamosas/sangue , Carcinoma de Células Escamosas/genética , Carcinoma de Células Escamosas/cirurgia , Ablação por Cateter/métodos , Feminino , Humanos , Pessoa de Meia-Idade , Invasividade Neoplásica , Estadiamento de Neoplasias , Valor Preditivo dos Testes , Prognóstico , Qualidade de Vida , Sensibilidade e Especificidade , Resultado do Tratamento , Neoplasias do Colo do Útero/sangue , Neoplasias do Colo do Útero/genética , Neoplasias do Colo do Útero/cirurgia
4.
Chirurgia (Bucur) ; 108(5): 611-5, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-24157103

RESUMO

AIM: Given the context that rectal tumours respond to a certain degree to radiotherapy, a necessity arises for estimating a tumour's capacity to react to radiation from the very moment of diagnostic biopsy. MATERIAL AND METHODS: We have histologically and immunohistochemically analysed tissues coming from 52 patients with rectal adenocarcinomas. RESULTS: Of the studied parameters, the ones presenting significant variation under radiotherapy in terms of statistics(p 0.05) were: colloid type (p=0.001), EGFR in the tumour(p=0.00045), EGFR in the normal epithelium (p=0.0017),VEGF in the tumour (p=0.0132) and VEGF in the tumour stroma (p=0.030). CONCLUSIONS: Our study follows the same trends as the medical literature we have consulted regarding the variation of EGFR and VEGF with radiotherapy, and the distinct note of our study relies in the observation that normal stroma in case of rectal tumors also reacts to radiotherapy, sometimes more aggressively than the tumor itself, especially in which concerns the nerve and muscle fibers.


Assuntos
Adenocarcinoma/patologia , Adenocarcinoma/radioterapia , Biomarcadores Tumorais/metabolismo , Receptores ErbB/metabolismo , Neoplasias Retais/patologia , Neoplasias Retais/radioterapia , Fator A de Crescimento do Endotélio Vascular/metabolismo , Adenocarcinoma/metabolismo , Biópsia , Feminino , Humanos , Imuno-Histoquímica , Masculino , Células Oxífilas/patologia , Valor Preditivo dos Testes , Prognóstico , Radioterapia Adjuvante , Neoplasias Retais/metabolismo , Estudos Retrospectivos , Sensibilidade e Especificidade
5.
Chirurgia (Bucur) ; 108(2): 152-60, 2013.
Artigo em Inglês | MEDLINE | ID: mdl-23618562

RESUMO

Mesenteric lymphadenitis constitutes a frequent cause for abdominal pain and may manifest acute abdominal symptoms. Very often, it is difficult to achieve a differential diagnosis as there are many diseases that can generate mesenteric lymphadenopathy. Many times, it is impossible to determine the diagnosis of the disease that has triggered mesenteric lymphadenopathy even after surgical intervention with biopsy. The failure in determining the precise cause of the mesenteric lymphadenoapathy, as well as its unresponsiveness to conservative treatments increases the difficulty in the management of this disease very much. In this paper we have reviewed the diseases that can trigger mesenteric lymphadenitis in detail, with reference to our experience. To the best of our knowledge, this is the most extensive review on this theme in current specific literature. The case reported by us, with a history of mesenteric adenitis, splenic and ganglionic abscesses, vasculitis skin nodules, pseudotumoral ileal stenosis and remission-recurrence pattern over 25 years, has raised extremely difficult problems of differential diagnosis. Its enlistment as a Crohn's disease, vasculitis or aseptic abscess syndrome seems unsatisfactory. The analysis of the data in this case can raise the legitimacy of the question: should we recognize and define a new entity?


Assuntos
Abscesso/diagnóstico , Doenças do Íleo/diagnóstico , Obstrução Intestinal/diagnóstico , Linfadenite Mesentérica/diagnóstico , Esplenopatias/diagnóstico , Vasculite Sistêmica/diagnóstico , Dor Abdominal/etiologia , Abscesso/complicações , Abscesso/etiologia , Abscesso/terapia , Adulto , Doença de Crohn/diagnóstico , Diagnóstico Diferencial , Feminino , Seguimentos , Humanos , Doenças do Íleo/complicações , Doenças do Íleo/etiologia , Doenças do Íleo/terapia , Obstrução Intestinal/complicações , Obstrução Intestinal/etiologia , Obstrução Intestinal/terapia , Linfadenite Mesentérica/complicações , Linfadenite Mesentérica/terapia , Recidiva , Esplenopatias/complicações , Esplenopatias/etiologia , Esplenopatias/terapia , Vasculite Sistêmica/complicações , Vasculite Sistêmica/terapia , Fatores de Tempo
6.
Rom J Intern Med ; 41(1): 95-8, 2003.
Artigo em Inglês | MEDLINE | ID: mdl-15529590

RESUMO

Wegener's disease (WD) which is mostly a systemic illness rarely presents as isolated, monoorganic, limited disease. Limited pharyngolaryngeal WD is thus a very rare occurrence. We report the case of a 29 years old man who developed a pharyngolaryngeal tumor with clinically benign evolution, histologically showing granulomatous inflammation and small vessel vasculitis, with no signs of: tuberculosis, sarcoidosis, fungal disease, Hodgkin's disease or foreign body aspiration. p-ANCA's were positive. He was considered a limited form of WD and treated with moderate doses of corticoids and cotrimoxazole. One month later, the lesion diminished significantly. The finding of a pharyngolaryngeal tumor with granulomatous inflammation and vasculitis, in the context of p-ANCA positivity and without any evidence for another systemic granulomatous disease, suggested the diagnosis of limited WD. The response to treatment favoured this presumption. Limited pharyngolaryngeal WD is a rare disease, with a potential for life-threatening (even fatal) complications. It should be recognized early and treated promptly. Remissions can be achieved (even without the use of cyclophosphamide).


Assuntos
Granulomatose com Poliangiite/diagnóstico , Neoplasias Laríngeas/etiologia , Neoplasias Faríngeas/etiologia , Adulto , Granulomatose com Poliangiite/complicações , Granulomatose com Poliangiite/patologia , Humanos , Masculino
7.
Virchows Arch ; 437(5): 555-9, 2000 Nov.
Artigo em Inglês | MEDLINE | ID: mdl-11147178

RESUMO

We report a rare case of biliary cystadenocarcinoma that occurred in the left hepatic lobe of a 62-year-old man and measured 20 cm in its greatest dimension. The neoplastic epithelium consisted of two types of cells: (1) cells with clear cytoplasm containing abundant mucin, and (2) cells with eosinophilic cytoplasm, which in some areas formed nodules with hepatocytoid features (polygonal cell shape, large nuclei with prominent nucleoli, and pseudoglandular structures). Histochemical stains revealed the presence of cytoplasmic mucin in the hepatocytoid areas, whereas immunohistochemical stains clearly showed a biliary phenotype (diffuse positive staining for "biliary type" cytokeratins, rare foci of positive staining with antibody to human hepatocytes (HEP-PAR1), absence of staining for alpha-fetoprotein, and no evidence of canalicular pattern of staining with polyclonal antibody to carcinoembryonic antigen). These findings indicate that areas reminiscent of hepatocellular carcinoma may occur in biliary cystadenocarcinomas. Histochemical and immunohistochemical stains are useful in reaching a definitive diagnosis in such cases.


Assuntos
Neoplasias dos Ductos Biliares/patologia , Ductos Biliares Intra-Hepáticos , Cistadenocarcinoma/patologia , Neoplasias dos Ductos Biliares/diagnóstico por imagem , Neoplasias dos Ductos Biliares/metabolismo , Cistadenocarcinoma/diagnóstico por imagem , Cistadenocarcinoma/metabolismo , Humanos , Imuno-Histoquímica , Masculino , Pessoa de Meia-Idade , Tomografia Computadorizada por Raios X
8.
Rom J Morphol Embryol ; 44(1-4): 45-9, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-15678842

RESUMO

Pulmonary carcinoid tumors are considered low grade malignant tumors, arising from neuroendocrine cells from bronchial mucosa. The small cell proliferation is arranged in small nests or trabeculae, the nuclei are round to oval with finely dispersed chromatin, indistinct nucleoli, small amount of cytoplasm, indistinct borders. Problems of differential diagnosis could appear in distinction with others malignancies like adenocarcinomas, squamous cell carcinomas, lymphomas and others neuroendocrine tumors, especially in the different prognosis and therapeutic approach. We described 15 cases of pulmonary carcinoid tumors diagnosticated by morphologic and immunohistochemical methods.


Assuntos
Tumor Carcinoide/patologia , Neoplasias Pulmonares/patologia , Adulto , Idoso , Tumor Carcinoide/metabolismo , Núcleo Celular/metabolismo , Núcleo Celular/patologia , Cromogranina A , Cromograninas/metabolismo , Diagnóstico Diferencial , Feminino , Humanos , Neoplasias Pulmonares/metabolismo , Masculino , Pessoa de Meia-Idade
10.
Rom J Morphol Embryol ; 44(1-4): 191-9, 1998.
Artigo em Inglês | MEDLINE | ID: mdl-15678863

RESUMO

Some malignant tumours like testicular seminomas and ovarian dysgerminomas or medullar carcinoma of the breast, present an unusually lympho-histiocytic (TIL) rich stroma. Many reports have concluded that the prognosis for these patients is correlated with the intensity of TIL. Recently, some analyses consider that tumour-host interactions have a significant prognostic role in many other neoplasms. The presence of TIL may be a sign of less aggressive behaviour of some epithelial neoplasm like gastro-intestinal, pulmonary, mammary, urinary or cutaneous carcinomas (Wilson et al.). The aim of this study is a morphological and immunohistochemical (IHC) characterisation of the lympho-histiocytic populations of TIL in some gastro-intestinal and mammary carcinomas. The two localisation were chosen for their different contact with the exogene antigens and their possible different type of host's immune response.


Assuntos
Adenocarcinoma/patologia , Neoplasias da Mama/patologia , Carcinoma Ductal/patologia , Neoplasias Colorretais/patologia , Linfócitos do Interstício Tumoral/patologia , Neoplasias Gástricas/patologia , Adenocarcinoma/metabolismo , Antígenos CD20/metabolismo , Neoplasias da Mama/metabolismo , Carcinoma Ductal/metabolismo , Neoplasias Colorretais/metabolismo , Feminino , Humanos , Antígenos Comuns de Leucócito/metabolismo , Subpopulações de Linfócitos/metabolismo , Subpopulações de Linfócitos/patologia , Linfócitos do Interstício Tumoral/metabolismo , Microscopia Eletrônica de Transmissão , Neoplasias Gástricas/metabolismo
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA
...