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1.
Zhongguo Xue Xi Chong Bing Fang Zhi Za Zhi ; 29(1): 108-110, 2017 Jan 19.
Artigo em Chinês | MEDLINE | ID: mdl-29469403

RESUMO

OBJECTIVE: To report the diagnosis and treatment of an imported case of schistosomiasis haematobium, including the pathological features of the disease and therapeutic efficacy of praziquantel. METHODS: The data of the patient with schistosomiasis haematobium were collected, and the pathological features of the bladder tissue were observed under a microscope. More-over, the patient was treated with praziquantel, and his urine was collected before and after the treatment. The eggs in the urine were examined by a microscope after sediment and the miracidia were hatched. RESULTS: The patient once worked in Angola for three months, and after returning home he had the symptoms of intermittent painless terminal hematuresis. It was ineffective after anti-inflammatory treatment in a number of hospitals. There were no sand spots discovered under the cystoscope. However, the inflammatory reaction to parasite with a lot of eosinophils infiltration in the bladder mucosa was found on the pathological sections under a microscope, and the egg structure was observed with individual characteristics. The eggs were detected in the urine and the miracidia were hatched before the praziquantel treatment. The hematuria symptoms disappeared after the praziquantel treatment. The eggs were still detected in the urine 7 days post-treatment, but the miracidium could not be hatched. One month and 6 months post-treatment, the eggs were not detected in the urine. CONCLUSIONS: The imported cases of schistosomiasis haematobium are often misdiagnosed, and therefore, it is necessary to strength the health education to the workers overseas and also to improve the ability of diagnosis in medical staff. For the case reported in this paper, there are typical structure of Schistosoma haematobium eggs and egg-granulomas on the pathological sections of bladder tissues. Praziquantel has satisfactory treatment results.


Assuntos
Anti-Helmínticos/uso terapêutico , Praziquantel/uso terapêutico , Esquistossomose Urinária/diagnóstico , Esquistossomose Urinária/tratamento farmacológico , Animais , Humanos , Masculino , Contagem de Ovos de Parasitas , Schistosoma haematobium/isolamento & purificação , Resultado do Tratamento
2.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-662466

RESUMO

Objective To relieve the influences of the respiratory motion on the liver contrast-enhance ultrasound (CEUS) image sequences,to enhance the quantitative analysis accuracy for liver CEUS and to put forward a correction strategy for the respiratory motion in liver CEUS sequences.Methods A principal component analysis (PCA) model of the respiratory motion in liver CEUS sequences was established with 18 cases of rabbit liver VX2 tumors,and a respiratory motion curve was generated based on the principal component with large data proportion,then the images with similar phases to the reference image were analyzed.Resnlts Correction made the mean structural similarity and mean correlation coefficient enhanced significantly to 0.57±0.11 and 0.78±0.11 respectively (P<0.001),while the average of deviation valve (DV) was decreased to 29.9±7.02 which only was one-third of the original value.Threshold setting could further improve the quality of the selected image sequence.Conchusion The proposed respiratory motion method proves its effectiveness for rabbit liver CEUS image sequences,and thus contributes to enhancing the differential diagnosis rate of benign and malignant liver tumors.

3.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-660097

RESUMO

Objective To relieve the influences of the respiratory motion on the liver contrast-enhance ultrasound (CEUS) image sequences,to enhance the quantitative analysis accuracy for liver CEUS and to put forward a correction strategy for the respiratory motion in liver CEUS sequences.Methods A principal component analysis (PCA) model of the respiratory motion in liver CEUS sequences was established with 18 cases of rabbit liver VX2 tumors,and a respiratory motion curve was generated based on the principal component with large data proportion,then the images with similar phases to the reference image were analyzed.Resnlts Correction made the mean structural similarity and mean correlation coefficient enhanced significantly to 0.57±0.11 and 0.78±0.11 respectively (P<0.001),while the average of deviation valve (DV) was decreased to 29.9±7.02 which only was one-third of the original value.Threshold setting could further improve the quality of the selected image sequence.Conchusion The proposed respiratory motion method proves its effectiveness for rabbit liver CEUS image sequences,and thus contributes to enhancing the differential diagnosis rate of benign and malignant liver tumors.

4.
Journal of Experimental Hematology ; (6): 1005-1008, 2015.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-357230

RESUMO

<p><b>OBJECTIVE</b>To explore the inhibitory effect of curcumin on proliferation of CD34(+) acute myeloid leukemia cells and its mechamism.</p><p><b>METHODS</b>KG1a and Kasumi-1cell lines were treated with curcumin of different concentrations (0, 40, 60, 80 µmol/L). The effect of curcumin on cell viability and proliferation was detected by trypan blue staining and cell count. The effect of curcumin on distribution of NF-κB P65 subunit was analyzed by immunofluorescence and Western blot.</p><p><b>RESULTS</b>The curcumin inhibited proliferation of KG1a and Kasumi-1 cells in a dose-dependent manner. Western blotting showed that curcumin led to significant down-regulation of NF-κB P65 nuclear protein expression. Immunofluorescence assay showed that treatment with 40 µmol/L of curcumin for 48h suppressed the nuclear translocation of NF-κB p65 in KG1a and Kasumi-1 cells.</p><p><b>CONCLUSION</b>The curcumin suppresses cell growth of KG1a and Kasumi-1 cells, its mechanism may be related to inhibitory effect of curcumin on NF-κB p65 nucleus protein.</p>


Assuntos
Humanos , Antígenos CD34 , Apoptose , Ciclo Celular , Linhagem Celular Tumoral , Proliferação de Células , Sobrevivência Celular , Curcumina , Regulação para Baixo , Leucemia Mieloide Aguda , NF-kappa B , Fator de Transcrição RelA
5.
Chinese Journal of Hematology ; (12): 748-751, 2010.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-353555

RESUMO

<p><b>OBJECTIVE</b>To compare the effectiveness and side effects of two chemotherapy regimens [pirarubicin + cytarabine (TA) and daunorubicin + cytarabine (DA)] in patients with acute myeloid leukemia (AML).</p><p><b>METHODS</b>From Oct 2006 to Jul 2009, there were 207 newly diagnosed AML patients randomized into DA or TA group from 72 centers all over the country. The aim of this clinical trial is to observe and evaluate complete remission rate (CR), total remission rate (TRR), and side effect after one or two circles of therapy.</p><p><b>RESULTS</b>In 198 evaluable patients, 126 cases in TA group and 72 in DA group were evalvable, with a ratio of 1.75:1. CR was 69.8% and TRR (CR + PR) was 81.8% in TA group and 63.9%, 80.9% in DA group, correspondingly (P > 0.05). For patients with subtype M(2), CR (77.1%) in TA group was higher than that in DA (60%). There was no difference in side effect between the two groups.</p><p><b>CONCLUSION</b>There is no difference of the effect between TA and DA chemotherapy for newly diagnosed AML patients. But for subtype M(2), TA is more efficacy. And there is no difference in side effect between the two regimens.</p>


Assuntos
Humanos , Protocolos de Quimioterapia Combinada Antineoplásica , Usos Terapêuticos , Citarabina , Daunorrubicina , Leucemia Mieloide Aguda , Tratamento Farmacológico , Estudos Prospectivos
6.
Artigo em Chinês | WPRIM (Pacífico Ocidental) | ID: wpr-253286

RESUMO

To investigate the combined effect of human recombinant soluble TNF-related apoptosis induced ligand (hrsTRAIL) with Ara-C or alone on HL-60 leukemia cell lines and its mechanism, human leukemia cell lines HL-60 were cultured in vitro. HL-60 cells were divided into 5 groups: control group, Ara-C group, rsTRAIL group, Ara-C + rsTRAIL simultaneously given group, Ara-C + rsTRAIL tandem given group (Ara-C followed by rsTRAIL group). The cytotoxic effect was measured by MTT assay; cell apoptosis rate was determined by flow cytometry after Annexin V/PI staining; the expression level of DR5 on surface of HL-60 cells treated with Ara-C at different concentrations for 24 hours was determined by flow cytometry. The expression level of DR5 on surface of HL-60 cells and caspase-8 activity in HL-60 cells of rsTRAIL group and Ara-C + rsTRAIL tandem group was determined by flow cytometry. The result showed that rsTRAIL could inhibit the proliferation of HL-60 cells and induce apoptosis of HL-60 cells in a concentration-dependent manner. The apoptosis rate of HL-60 cells in Ara-C + rsTRAIL tandem given group was higher than that in Ara-C + rsTRAIL simultaneously given group, the expression level of DR5 on surface of HL-60 cells and intracellular activity of caspase-8 in Ara-C + rsTRAIL tandem given group were higher than those in rsTRAIL group. When HL-60 cells treated with 5 and 10 mg/L of Ara-C for 24 hours, the expression level of DR5 on surface of HL-60 cells was higher than that in control group. It is concluded that rsTRAIL can inhibit the proliferation of HL-60 cells, and induce apoptosis of HL-60 cells. Ara-C can upregulate DR5 expression on the surface of HL-60 cells and enhance the effect of rsTRAIL-inducing apoptosis. Tandem treatment of HL-60 cells with Ara-C followed by rsTRAIL induce more apoptosis than that of co-treatment with rsTRAIL and Ara-C. Ara-C and rsTRAIL has a synergistic inhibitory effect on growth of HL-60 cells. The mechanism may correlate with up-regulation of the expression level of DR5 and/or caspase-8 in HL-60 cells by Ara-C.


Assuntos
Humanos , Apoptose , Caspase 8 , Genética , Metabolismo , Proliferação de Células , Citarabina , Farmacologia , Relação Dose-Resposta a Droga , Sinergismo Farmacológico , Células HL-60 , Receptores do Ligante Indutor de Apoptose Relacionado a TNF , Genética , Metabolismo , Proteínas Recombinantes , Farmacologia , Ligante Indutor de Apoptose Relacionado a TNF , Farmacologia , Regulação para Cima
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