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3.
Diagn Cytopathol ; 15(5): 431-4, 1996 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-8989549

RESUMO

We describe the cytologic findings of a fine-needle aspiration (FNA) breast lesion with a typical histology for adenoid cystic carcinoma. The aspirate yielded highly cellular smears with a monomorphic population of small, slightly atypical cells, arranged in multilayered groups with abundant fine intercellular metachromatic substance between cell groups. There were also fragments of fibrillar stroma in close relation to epithelial cells. The diagnosis based on the FNA material was suspicious of malignancy. The cytomorphology in this case presented a difficult differential diagnosis with pleomorphic adenoma. Features indicative of adenoid cystic carcinoma were nuclear cell hyperchromasia, the presence of small nucleoli, and scant, poorly defined, or absent cytoplasms. Differential diagnosis of breast adenoid cystic carcinoma with other entities will also be discussed.


Assuntos
Adenoma Pleomorfo/patologia , Neoplasias da Mama/patologia , Carcinoma Adenoide Cístico/patologia , Adenoma Pleomorfo/ultraestrutura , Idoso , Biópsia por Agulha , Neoplasias da Mama/ultraestrutura , Calcinose , Carcinoma Adenoide Cístico/ultraestrutura , Diagnóstico Diferencial , Feminino , Histocitoquímica , Humanos
4.
Cancer ; 65(8): 1692-9, 1990 Apr 15.
Artigo em Inglês | MEDLINE | ID: mdl-2156597

RESUMO

The current trial was carried out to assess the survival enhancement achieved, if any, by adding ifosfamide to vindesine and cisplatin (IVP) in contrast to mitomycin plus vindesine and cisplatin (MVP). Between June 1986 and September 1988, 110 patients were randomly allocated to receive either ifosfamide (3 g/m2 plus 3 g/m2 of mesna) or mitomycin 8 mg/m2, on days 1, 29, and 71 only. In both arms vindesine was given 3 mg/m2 weekly X 5 then every 2 weeks. In the MVP arm, 120 mg/m2 of cisplatin was administered on days 1 and 29 and then every 6 weeks, whereas in the IVP arm 100 mg/m2 of cisplatin was given on the same time schedule. One hundred three patients were evaluable for response and toxicity and 56% of patients had Mountain's Stage IV disease. The response rate was 26% (14/53 patients) in the MVP arm (95% confidence interval, 14%-39%) and 20% (ten of 50 patients) in the IVP arm (95% confidence interval, 10%-34%). Neither the response rate nor the median survival times were significantly different, although more nephrotoxicity was produced in the MVP arm, grade 1+ in 43% versus 26% in IVP arm (P = 0.04). Results obtained from this study fail to demonstrate that mitomycin or ifosfamide have a synergistic effect on the efficacy of the vindesine/cisplatin combination.


Assuntos
Protocolos de Quimioterapia Combinada Antineoplásica/uso terapêutico , Carcinoma Pulmonar de Células não Pequenas/tratamento farmacológico , Cisplatino/administração & dosagem , Ifosfamida/administração & dosagem , Neoplasias Pulmonares/tratamento farmacológico , Mitomicinas/administração & dosagem , Vindesina/administração & dosagem , Adulto , Idoso , Protocolos de Quimioterapia Combinada Antineoplásica/efeitos adversos , Carcinoma Pulmonar de Células não Pequenas/enzimologia , Cisplatino/efeitos adversos , Protocolos Clínicos , Feminino , Humanos , Ifosfamida/efeitos adversos , L-Lactato Desidrogenase/sangue , Neoplasias Pulmonares/enzimologia , Masculino , Pessoa de Meia-Idade , Mitomicina , Mitomicinas/efeitos adversos , Distribuição Aleatória , Indução de Remissão , Taxa de Sobrevida , Vindesina/efeitos adversos
5.
Arch Dermatol ; 125(9): 1218-24, 1989 Sep.
Artigo em Inglês | MEDLINE | ID: mdl-2774597

RESUMO

Liver biopsy specimens from 168 patients who underwent a total of 364 biopsies were examined. Of 83 patients receiving biopsies before methotrexate treatment, 14 had one or more risk factors predictive of liver abnormality but they had normal pretreatment biopsy specimens. Among 17 patients with abnormal biopsy specimens before methotrexate treatment, only 1 had an identifiable risk factor and 5 had abnormal results of liver function tests. The probability of a normal biopsy specimen after methotrexate treatment dropped below 50% at a cumulative methotrexate dose of 3115 mg for the 31 patients with biopsy specimens from before and after methotrexate treatment and 5776 mg for those who had biopsies only after methotrexate treatment; this difference was statistically significant and is thought to be related to the fact that the patients who had biopsies before and after methotrexate treatment had received most of their medication by the parenteral rather than the oral route. A significant association existed between biopsy grade after methotrexate treatment and obesity. Other risk factors were not correlated with biopsy grade. Blood chemistry tests were not predictive of histopathologic findings. Eight of 11 patients with fibrosis or cirrhosis showed meaningful improvement in liver histologic findings after methotrexate treatment had been withdrawn for 6 months or more; none had progression of abnormalities.


Assuntos
Fígado/patologia , Metotrexato/administração & dosagem , Psoríase/tratamento farmacológico , Adolescente , Adulto , Idoso , Consumo de Bebidas Alcoólicas , Biópsia , Esquema de Medicação , Feminino , Humanos , Fígado/efeitos dos fármacos , Testes de Função Hepática , Masculino , Metotrexato/uso terapêutico , Pessoa de Meia-Idade , Fatores de Risco , Fatores de Tempo
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