Your browser doesn't support javascript.
loading
Mostrar: 20 | 50 | 100
Resultados 1 - 6 de 6
Filtrar
Adicionar filtros








Intervalo de ano
1.
Chinese Medical Sciences Journal ; (4): 377-382, 2020.
Artigo em Inglês | WPRIM | ID: wpr-879301

RESUMO

We present a 29-year-old woman with pT2N0M0 breast cancer, histological diagnosis of invasive ductal carcinoma, ER and PR low positive, and HER-2 (3+). The patient developed trastuzumab-induced thrombocytopenia in 6 hours after an intravenous infusion of trastuzumab at the second cycle of trastuzumab treatment with the symptom of abnormal uterine bleeding. Laboratory exam revealed a sharp drop of platelet count down to 3×10

2.
Acta Academiae Medicinae Sinicae ; (6): 607-610, 2016.
Artigo em Inglês | WPRIM | ID: wpr-277932

RESUMO

Implant-based breast reconstruction is the most common choice in breast cancer patients. Recently,the acellular dermal matrix (ADM) technique has been widely used in implant-based breast reconstruction in the western countries. This article briefly reviews the biological characteristics,history,types,surgical techniques,and postoperative complications of ADM.


Assuntos
Feminino , Humanos , Derme Acelular , Implante Mamário , Implantes de Mama , Neoplasias da Mama , Cirurgia Geral , Mastectomia , Complicações Pós-Operatórias
3.
Journal of Southern Medical University ; (12): 1047-1050, 2011.
Artigo em Chinês | WPRIM | ID: wpr-235200

RESUMO

<p><b>OBJECTIVE</b>To evaluate the value of cardiac troponin I (CTnI) measurement in predicting anthracycline-induced cardiotoxicity in patients with breast cancer.</p><p><b>METHODS</b>This study was conducted among 186 breast cancer patients receiving anthracycline-based chemotherapy. Serum cTnI concentrations before and after each cycle of the chemotherapy and the left ventricular ejection fraction (LVEF) before and at the 2nd, 4th and 6th months of the treatment were recorded. According to serum cTnI concentration, the patients were divided into CTnI+ group (with serum CTnI concentration of no less than 0.1 ng/ml, n=60) and CTnI- (<0.1 ng/ml) group (n=126).</p><p><b>RESULTS</b>No patients in this series experienced cardiac heart failure (CHF). The number of patients with a LVEF reduction by over 10% from the baseline was 16 (26.7%) in CTnI+ group, as compared to 7 (5.6%) in CTnI- group, showing a significant difference between the two groups (P<0.01).</p><p><b>CONCLUSION</b>CTnI can be a useful marker for early prediction of anthracycline-induced cardiotoxicity in patients with breast cancer.</p>


Assuntos
Adulto , Idoso , Feminino , Humanos , Pessoa de Meia-Idade , Adulto Jovem , Antraciclinas , Usos Terapêuticos , Antibióticos Antineoplásicos , Usos Terapêuticos , Biomarcadores , Sangue , Neoplasias da Mama , Tratamento Farmacológico , Cardiotoxinas , Miocárdio , Metabolismo , Troponina I , Sangue
4.
Journal of Southern Medical University ; (12): 2301-2303, 2010.
Artigo em Chinês | WPRIM | ID: wpr-323676

RESUMO

<p><b>OBJECTIVE</b>To investigate the feasibility of D2-40 labeling for detecting lymphatic vessels in breast cancer tissues and the clinicopathological implications of lymphatic vessel invasion (LVI).</p><p><b>METHODS</b>Immunohistochemistry was used to detect the expression of D2-40 and lymphatic invasion in 72 cases of breast cancer and 15 benign breast tumor tissues, and their correlations to the clinicopathological factors were analyzed.</p><p><b>RESULTS</b>The positivity rate of LVI was 69.4% in breast cancer tissue. In patients with lymph node metastasis, the positivity rate of LVI was significantly higher than that in patients without lymph node involvement (85.7% vs 54.1%, P<0.01), and LVI was found to be positively correlated to axillary lymph node metastasis (r=0.382).</p><p><b>CONCLUSION</b>D2-40 can specially and reliably mark the lymphatic vessels in breast cancer tissues. LVI is positively correlated to axillary lymph node metastasis and occurs earlier than the latter, therefore should be included in routine clinicopathological testing.</p>


Assuntos
Adulto , Idoso , Feminino , Humanos , Pessoa de Meia-Idade , Anticorpos Monoclonais , Neoplasias da Mama , Diagnóstico , Patologia , Imuno-Histoquímica , Métodos , Linfonodos , Patologia , Metástase Linfática , Diagnóstico , Patologia , Vasos Linfáticos , Patologia , Estadiamento de Neoplasias
5.
Journal of Southern Medical University ; (12): 1548-1551, 2010.
Artigo em Chinês | WPRIM | ID: wpr-336145

RESUMO

<p><b>OBJECTIVE</b>To investigate the expression of D2-40 and CD34 in invasive ductal carcinoma of the breast and the clinical significance.</p><p><b>METHODS</b>D2-40 and CD34 expressions were detected immunohistochemically in 108 cases of invasive ductal carcinoma of the breast and 30 cases of breast fibroadenoma. The lymphatic microvessel density (LMD) and the microvessel density (MD), marked by D2-40 and CD34, respectively, were calculated and their relationship with the clinicopathological factors was analyzed.</p><p><b>RESULTS</b>The LMD and MD for invasive ductal carcinoma of the breast were significantly higher than those of breast fibroadenoma (P<0.01). One-way ANOVA indicated that the LMD differed significantly between tumors of different histological grades, status of lymph node metastasis and TNM stages; the MD also varied significantly with the tumor size, histological grade, lymph node metastasis and TNM stage. The LMD and MD showed a positive correlation to the tumor size (r=0.335, 0.337), histological grade (r=0.580, 0.671), lymph node metastasis (r=0.690, 0.721) and TNM stage (r=0.623, 0.634), but not to ER, PR or Her-2 status (P>0.05).</p><p><b>CONCLUSIONS</b>D2-40 can specifically mark the lymphatic endothelial cells in invasive ductal carcinoma of the breast. The LMD and MD are positively correlated to the clinicopathological factors of the malignancy. D2-40 and CD34 has the potential for use as the predictors to evaluate the tumor progression and metastasis.</p>


Assuntos
Adulto , Idoso , Feminino , Humanos , Pessoa de Meia-Idade , Adulto Jovem , Antígenos CD34 , Metabolismo , Biomarcadores Tumorais , Metabolismo , Neoplasias da Mama , Metabolismo , Patologia , Carcinoma Ductal de Mama , Metabolismo , Patologia , Vasos Linfáticos , Microvasos , Estadiamento de Neoplasias , Prognóstico
6.
Chinese Journal of Surgery ; (12): 1349-1352, 2006.
Artigo em Chinês | WPRIM | ID: wpr-288591

RESUMO

<p><b>OBJECTIVE</b>To investigate the effects of mutant exogenous P27(kip1) gene on chemosensitivity of human cholangiocarcinoma cell line.</p><p><b>METHODS</b>The recombinant vector was constructed and the mutant P27(kip1) gene was transfected into human cholangiocarcinoma cell line (QBC(939)). RT-PCR and Western blot were used to determine the expression of target genes. The effects of 5-fluorouracil (5-FU), mitomycin C (MMC) and cyclophosphamide (CTX) on the transfected cells were detected by assaying the apoptotic rate and growth inhibition by methabenzthiazuron (MTT) assay and flow cytometry (FCM).</p><p><b>RESULTS</b>The mutant exogenous P27(kip1) gene was expressed effectively in the cells, and the expression enhanced the apoptosis and growth inhibition of QBC(939) inducted by 5-FU, MMC and CTX. The ratio of growth inhibiting increased significantly from 41.89% (5-FU), 45.59% (MMC), 38.91% (CTX) to 56.15% (5-FU), 55.65% (MMC), 51.69% (CTX), and apoptosis index from 13.76% +/- 3.03% (5-FU), 11.76% +/- 3.99% (MMC), 10.46% +/- 2.10% (CTX) to 41.39% +/- 4.32% (5-FU), 35.94% +/- 2.71% (MMC), 34.46% +/- 2.32% (CTX) (P < 0.05).</p><p><b>CONCLUSIONS</b>The exogenous P27(kip1) gene transfer can remarkably increase the drug sensibility of the cholangiocarcinoma cells. The strategy targeted to control the cell cycle may be more effective in cancer treatment by combination of P27(kip1) gene therapy.</p>


Assuntos
Humanos , Adenoviridae , Genética , Antineoplásicos , Farmacologia , Apoptose , Neoplasias dos Ductos Biliares , Patologia , Ductos Biliares Intra-Hepáticos , Divisão Celular , Linhagem Celular Tumoral , Colangiocarcinoma , Patologia , Inibidor de Quinase Dependente de Ciclina p27 , Genética , Farmacologia , Sinergismo Farmacológico , Vetores Genéticos , Transfecção
SELEÇÃO DE REFERÊNCIAS
DETALHE DA PESQUISA