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2.
AJR Am J Roentgenol ; 180(1): 121-8, 2003 Jan.
Artigo em Inglês | MEDLINE | ID: mdl-12490490

RESUMO

OBJECTIVE: The aim of our prospective study was to assess the MR imaging characteristics of hepatic metastases of neuroendocrine tumors and to determine the optimal MR sequence for their detection. SUBJECTS AND METHODS: Thirty-seven consecutive patients with liver metastases from neuroendocrine tumors underwent 1.5-T MR imaging of the liver comprising T2-weighted fast spin-echo with respiratory monitoring, breath-hold T2-weighted single-shot fast spin-echo, and T1-weighted gradient-recalled echo sequences before and after the injection of gadoterate dimeglumine. Images were reviewed independently by three observers for the number, location, and pattern of signal and enhancement of metastases. RESULTS: A total of 359 metastases were detected, 279 on T2-weighed fast spin-echo, 231 on T2-weighed single-shot fast spin-echo, 272 on unenhanced T1-weighted, 322 on hepatic arterial phase, and 228 on portal venous phase images. Hepatic arterial phase images revealed the greatest number of metastases in 70% of patients, including 35 metastases seen only on this sequence, and was significantly superior to the unenhanced T1-weighted and portal venous phase sequences (p < 0.01). The lesion-to-liver contrast was significantly greatest with T2-weighed fast spin-echo sequences. The enhancement patterns of metastases were predominantly hypervascular, hypovascular, peripheral with progressive fill-in, and delayed in, respectively, 27, four, four, and two patients. Most metastases with peripheral enhancement and progressive fill-in were heterogeneous on T2-weighted images and were without globular peripheral enhancement. CONCLUSION: Hepatic metastases of neuroendocrine tumors had a typical hypervascular pattern in 73% of patients. Hepatic arterial phase and fast spin-echo T2-weighed sequences are the most sensitive.


Assuntos
Neoplasias Hepáticas/secundário , Imageamento por Ressonância Magnética/métodos , Tumores Neuroectodérmicos/secundário , Adulto , Idoso , Feminino , Humanos , Aumento da Imagem , Neoplasias Hepáticas/irrigação sanguínea , Neoplasias Hepáticas/diagnóstico , Masculino , Pessoa de Meia-Idade , Tumores Neuroectodérmicos/irrigação sanguínea , Tumores Neuroectodérmicos/diagnóstico , Estudos Prospectivos
3.
J Neurooncol ; 58(2): 131-6, 2002 Jun.
Artigo em Inglês | MEDLINE | ID: mdl-12164684

RESUMO

The hypothesis that tumor growth depends on neovascularization has been broadly used in oncology research. TNP-470 is a fumagillin synthetic analog that is isolated from Aspergillus fumigatus, and experimental studies suggested that it shows antitumor effect mediated by its strong antiangiogenic effect. Because limited experience exists about the antitumoral effect of TNP-470 in cerebral tumors, we have carried out a study in order to evaluate the effect of TNP-470 on tumor growth and the vascular area in an experimental malignant neuroectodermic tumor growing in the subcutaneous space of immunocompetent Wistar rats. Our results showed a significant tumor growth inhibition in animals treated with TNP-470 when compared to those in the control group (intratumoral injections were administered in 30 mg/kg dose, three times a week on alternate days during four consecutive weeks). Since the quantitative analysis of tumor vascular parameters--number of microvessels and total intratumor vascular area--in the experimental groups did not show significant statistical differences, we conclude that TNP-470 has a significant antitumor effect on our neuroectodermic tumor, but this effect is mediated by other antineoplastic mechanisms that are independent of its previously described angiostatic capacity.


Assuntos
Inibidores da Angiogênese/farmacologia , Antibióticos Antineoplásicos/farmacologia , Neovascularização Patológica/patologia , Tumores Neuroectodérmicos/irrigação sanguínea , Tumores Neuroectodérmicos/patologia , Sesquiterpenos/farmacologia , Neoplasias Cutâneas/irrigação sanguínea , Neoplasias Cutâneas/patologia , Animais , Cicloexanos , Antígeno Ki-67/metabolismo , Neoplasias Experimentais/metabolismo , Neoplasias Experimentais/patologia , Tumores Neuroectodérmicos/metabolismo , O-(Cloroacetilcarbamoil)fumagilol , Ratos , Ratos Wistar , Neoplasias Cutâneas/metabolismo
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