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1.
J Surg Oncol ; 87(2): 75-9, 2004 Aug 01.
Artículo en Inglés | MEDLINE | ID: mdl-15282699

RESUMEN

BACKGROUND AND OBJECTIVE: The aim of this study is to know whether intravenous digital subtraction angiography (IV-DSA) is useful to detect axillary lymph node metastasis of breast cancer and to evaluate the anigiogenesis of lymph nodes in the axilla. PATIENTS AND METHODS: Forty three primary breast cancer patients (N0: 26 cases, N1: 5 cases, N2: 2 cases) who underwent IV-DSA between January and November 2000 were included in the study. Infinix CB apparatus (Toshiba, Japan) was used to collect IV-DSA images and when a mass became stained in the axilla, it was considered to be metastatic. The angiogenesis was studied by examining microvessel density (MVD) after lymph node immunostaining for factor VIII. Primary tumor was detected by IV-DSA in all 43 cases. RESULTS: Axillary lymph node metastases were detected by IV-DSA in 34.9% of cases (15/43), and by pathology in 37.2% (16/43). The sensitivity, specificity, and accuracy of the diagnostic method were 75.0% (12/16), 88.9% (24/27), and 83.7% (36/43), respectively. MVD, calculated after immunostaining for factor VIII, was significantly lower in the in metastatic region of lymph nodes identified by DSA (88.5 +/- 35.0) than in metastasis-free lymph nodes (141.1 +/- 34.0, P < 0.0001). CONCLUSIONS: IV-DSA is useful in the diagnosis of axillary lymph node metastasis of breast cancer. Our results suggest that the primary factors involved in the mechanism of DSA display may be different from high/low MVC values.


Asunto(s)
Angiografía de Substracción Digital , Neoplasias de la Mama/diagnóstico por imagen , Neoplasias de la Mama/patología , Ganglios Linfáticos/patología , Axila , Neoplasias de la Mama/irrigación sanguínea , Factor VIII/análisis , Femenino , Humanos , Inmunohistoquímica , Metástasis Linfática , Neovascularización Patológica/diagnóstico por imagen , Sensibilidad y Especificidad
2.
Breast Cancer ; 10(4): 371-3, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-14634518

RESUMEN

We report a case of diabetic mastopathy with multiple unilateral lesions in an insulin dependent patient. The patient was a 62-year-old woman with two hard tumors in the right breast, who had been treated with insulin for diabetes mellitus. Mammography revealed a highly dense tumor in the right breast, while ultrasonography showed two irregular hypoechoic lesions with marked posterior acoustical shadowing, suggesting scirrhous carcinoma. On magnetic resonance imaging the two lesions had slightly heterogeneous enhancement. Aspiration breast cytology showed insufficient cellular material for evaluation. Excisional biopsy was performed because the patient wanted confirmation and treatment. Fibrosis with dense lymphocytic infiltration around the lobules and ducts was diagnosed histopathologically. These findings were compatible with diabetic fibrous mastopathy. Although this disease is thought to be a diabetes-induced reaction of autoimmune origin, multiple lesions are rare. This is the first case of unilateral multiple lesions of diabetic mastopathy.


Asunto(s)
Diabetes Mellitus Tipo 1/complicaciones , Enfermedad Fibroquística de la Mama/diagnóstico , Enfermedad Fibroquística de la Mama/etiología , Neoplasias de la Mama/diagnóstico , Diagnóstico Diferencial , Femenino , Enfermedad Fibroquística de la Mama/cirugía , Humanos , Mamografía , Mastectomía Segmentaria , Persona de Mediana Edad , Tomografía Computarizada por Rayos X , Ultrasonografía Mamaria
3.
Anticancer Res ; 23(4): 3215-21, 2003.
Artículo en Inglés | MEDLINE | ID: mdl-12926055

RESUMEN

Cyclooxygenase-2 (COX-2) is reported to play an important role in carcinogenesis. We examined COX-2 expression in patients with breast cancer and benign breast tumors. Immunohistochemical staining revealed a high level of COX-2 expression in malignant lesions of invasive ductal carcinoma (IDC) at a rate of 40% and a low level of expression in 15% of adjacent normal-appearing breast epithelia. Similarly, in ductal carcinoma in situ (DCIS), a high level of COX-2 expression was found in 80% of malignant lesions and a low level of expression in 50% of normal epithelia. Reverse transcriptional polymerase chain reaction (RT-PCR) performed in 7 of these cases disclosed that COX-2 expression was restricted to the malignant lesion. Further, all 10 cases of fibroadenoma and 10 cases of intraductal papilloma, both of which are benign tumors, had a high level of COX-2 expression. When overexpression of COX-2 was analyzed in relation to the clinicopathological features of the patients, no characteristic correlation was noted. Our results demonstrated that COX-2 is expressed in mammary tissue during tumorigenesis of the breast gland, suggesting that the cyclooxygenase isoenzyme may be a target for the prevention and treatment of breast cancer.


Asunto(s)
Neoplasias de la Mama/enzimología , Isoenzimas/biosíntesis , Prostaglandina-Endoperóxido Sintasas/biosíntesis , Neoplasias de la Mama/patología , Carcinoma in Situ/enzimología , Carcinoma Ductal de Mama/enzimología , Ciclooxigenasa 2 , Femenino , Fibroadenoma/enzimología , Humanos , Inmunohistoquímica , Proteínas de la Membrana , Papiloma Intraductal/enzimología , Reacción en Cadena de la Polimerasa de Transcriptasa Inversa
4.
Int J Clin Oncol ; 7(5): 322-5, 2002 Oct.
Artículo en Inglés | MEDLINE | ID: mdl-12402068

RESUMEN

Intravenous digital subtraction angiography (IV-DSA) was performed before and after neoadjuvant chemotherapy (NACT) in five patients with locally advanced breast cancer, and the efficacy of NACT was evaluated on the basis of the results of IV-DSA and histopathological examination. Following NACT, the maximum density of tumor enhancement (MAX) in the IV-DSA image decreased by 61.6% in case 1, 50% in case 2, 58.1% in case 3, 90.8% in case 4, and 97.2% in case 5. In all five patients, the efficacy of chemotherapy was rated as a partial response in terms of tumor size, while histological efficacy was rated as slightly effective in cases 1-4 and moderately effective in case 5. The pathological efficacy of NACT was highest in case 5, which showed the greatest decrease in MAX. These results indicate that variations in MAX reflect clinical efficacy, and, to some extent, also permit prediction of pathological efficacy.


Asunto(s)
Angiografía de Substracción Digital , Neoplasias de la Mama/tratamiento farmacológico , Técnica de Sustracción , Neoplasias de la Mama/irrigación sanguínea , Neoplasias de la Mama/diagnóstico por imagen , Quimioterapia Adyuvante , Medios de Contraste/administración & dosificación , Femenino , Humanos , Inyecciones Intravenosas , Yopamidol/administración & dosificación , Persona de Mediana Edad
5.
Breast Cancer ; 9(3): 208-15, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12185331

RESUMEN

BACKGROUND: We have defined 18 chromosomal regions in which allelic losses were frequent among breast cancers. We examined whether specific allelic losses might correlate with any clinicopathological factors. METHODS: We tested DNA from matched normal and tumor tissues for loss of heterozygosity (LOH) at 18 microsatellite loci from a cohort of 504 patients who had undergone surgery for breast cancer. RESULTS: LOH at 3p14.3 correlated with a larger size of tumor (greater than 2 cm). LOH at 1p22, 3p25.1, 3p14.3, or 17q21.1 correlated with loss of estrogen receptors. LOH at as many as eleven regions correlated with loss of progesterone receptor, suggesting that these represent general phenomena associated with progression of cancer. Above all, allelic losses at 11q23-24, 13q12, 17p13.3, or 22q13 significantly correlated with lymph-node metastasis (11q23-24, p= 0.0042; 13q12, p=0.0207; 17p13.3, p=0.0478; 22q13, p=0.0162). CONCLUSION: These results suggest that some clinical characteristics of breast cancers are determined by loss of tumor suppressor genes present at specific chromosome regions. Especially, LOH at 11q23-24, 13q12, 17p13.3, and 22q13 is a significant predictor of lymph-node metastasis for patients who have undergone surgery for breast cancer, and may serve as a negative prognostic indicator.


Asunto(s)
Neoplasias de la Mama/genética , Neoplasias de la Mama/patología , Cromosomas Humanos/genética , Genes BRCA1 , Predisposición Genética a la Enfermedad , Pérdida de Heterocigocidad/genética , Ganglios Linfáticos/patología , Adulto , Anciano , Anciano de 80 o más Años , Alelos , Biopsia con Aguja , Neoplasias de la Mama/cirugía , Cromosomas Humanos Par 11 , Cromosomas Humanos Par 13 , Cromosomas Humanos Par 17 , Cromosomas Humanos Par 22 , Estudios de Cohortes , Técnicas de Cultivo , ADN de Neoplasias/análisis , Femenino , Marcadores Genéticos/genética , Humanos , Metástasis Linfática , Repeticiones de Microsatélite , Persona de Mediana Edad , Estadificación de Neoplasias , Probabilidad , Pronóstico , Receptores de Estrógenos/análisis , Receptores de Progesterona/análisis , Estudios Retrospectivos , Sensibilidad y Especificidad
6.
Breast Cancer ; 9(2): 166-9, 2002.
Artículo en Inglés | MEDLINE | ID: mdl-12016397

RESUMEN

We describe a patient with anthracycline-pretreated and docetaxel-refractory metastatic breast cancer who achieved a complete response after third-line chemotherapy with paclitaxel. A 59-year-old woman underwent modified radical mastectomy for advanced cancer in her left breast after local arterial neoadjuvant chemotherapy with anthracycline. Postoperatively anthracycline-containing adjuvant therapy was administered. Pulmonary metastases occurred 15 months after surgery, which did not respond to 4 cycles of second-line chemotherapy with docetaxel, given at 60 mg/m(2) every 3 weeks. Therefore 210 mg/m(2) of paclitaxel was given every 3 weeks as third-line monotherapy and induced a complete response with grade 3 neutropenia and hair loss as the major adverse effects. We suggest that paclitaxel is potentially effective as third-line monotherapy for anthracycline-resistant and docetaxel-refractory metastatic breast cancer.


Asunto(s)
Antineoplásicos Fitogénicos/administración & dosificación , Neoplasias de la Mama/tratamiento farmacológico , Neoplasias de la Mama/patología , Resistencia a Múltiples Medicamentos , Neoplasias Pulmonares/secundario , Paclitaxel/análogos & derivados , Paclitaxel/administración & dosificación , Taxoides , Antraciclinas/administración & dosificación , Protocolos de Quimioterapia Combinada Antineoplásica/administración & dosificación , Biopsia con Aguja , Neoplasias de la Mama/cirugía , Quimioterapia Adyuvante , Docetaxel , Femenino , Estudios de Seguimiento , Humanos , Neoplasias Pulmonares/tratamiento farmacológico , Neoplasias Pulmonares/patología , Mastectomía Radical Modificada/métodos , Estadificación de Neoplasias , Medición de Riesgo , Insuficiencia del Tratamiento , Resultado del Tratamiento
7.
Cancer Lett ; 180(1): 75-82, 2002 Jun 06.
Artículo en Inglés | MEDLINE | ID: mdl-11911973

RESUMEN

To identify specific allelic losses that might correlate with postoperative mortality of breast cancer patients treated with high-dose adjuvant chemotherapy consisting of cyclophosphamide, methotrexate and fluorouracil, we examined tumors from a cohort of 150 such patients, who were followed clinically for 5 years postoperatively, for allelic losses (loss of heterozygosity, LOH) among 18 microsatellite markers throughout the genome. Patients whose tumors had lost an allele at 8p22 had significantly higher risks of mortality than those whose tumors retained both alleles at those loci. At 8p22, the 5-year mortality rate was 31% among patients with losses vs. 8% with retention (P=0.0354). No other region showed correlation between LOH and prognosis. The data indicate that LOH at 8p22 is a significant predictor of postoperative mortality for breast cancer patients who received high-dose postoperative adjuvant chemotherapy. Thus, LOH at 8p22 can serve as a negative prognostic indicator to guide postoperative management of patients.


Asunto(s)
Alelos , Neoplasias de la Mama/diagnóstico , Neoplasias de la Mama/genética , Quimioterapia Adyuvante , Cromosomas Humanos Par 8 , Adulto , Anciano , Neoplasias de la Mama/tratamiento farmacológico , Femenino , Humanos , Pérdida de Heterocigocidad , Repeticiones de Microsatélite , Persona de Mediana Edad , Análisis Multivariante , Pronóstico , Factores de Tiempo
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