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1.
Prostate ; 62(2): 140-7, 2005 Feb 01.
Artigo em Inglês | MEDLINE | ID: mdl-15389803

RESUMO

BACKGROUND: The aim of this study was to visualize early stage prostate cancer (Cap) in a clinical setting. In previous studies, the results of magnetic resonance imaging (MRI) for screening Cap have rarely been confirmed by well-designed multisite prostate biopsy. METHODS: The prostate glands of 90 men with elevated prostate-specific antigen (PSA) were imaged by dynamic contrast-enhanced MRI (DCE-MRI) before transrectal ultrasound-guided 14-cores prostate biopsy. Each core was divided into three subcore fractions (total of 42 fractions) to generate a histological localization diagram, which was compared with localization-visualized DCE-MRI. RESULTS: The detection rate of Cap in 57 patients with PSA < 10.0 ng/ml was 36.8% as determined by the initial biopsy. DCE-MRI uncovered 92.9% of the clinically significant Caps and its specificity was 96.2% for the first biopsy session. One case with positive DCE-MRI and a negative primary biopsy was positive with additional biopsies. All of 26 DCE-MRI positive cases had significant Cap, and two of eight patients with histological Cap and negative or equivocal imaging had significant cancer. In total, 9 of 20 cases with DCE-MRI stage T2 underwent radical prostatectomy. All of them had organ-confined disease, although 33-77% (mean 63%) of them were expected to be rated T3 or higher by Partin's table. CONCLUSIONS: DCE-MRI can identify early stage Cap with high sensitivity and specificity, and can predict the histological grade to some extent. DCE-MRI prior to biopsy should be applied to younger patients with surgical indications. Otherwise, we recommend the definitive diagnosis of Cap by utilizing DCE-MRI alone.


Assuntos
Imageamento por Ressonância Magnética/métodos , Estadiamento de Neoplasias/métodos , Neoplasias da Próstata/patologia , Idoso , Biópsia , Diagnóstico Precoce , Humanos , Masculino , Pessoa de Meia-Idade , Antígeno Prostático Específico/sangue , Sensibilidade e Especificidade
2.
Prostate ; 60(4): 282-8, 2004 Sep 01.
Artigo em Inglês | MEDLINE | ID: mdl-15264238

RESUMO

BACKGROUND: Exclusion of prostatitis in screening for prostate cancer (Cap) is a matter of concern in the prostate-specific antigen (PSA) era. Yet, the identification of acute bacterial prostatitis (ABP), intentionally utilizing PSA in patients with pyrexia has been scarcely reported. METHODS: In total, 39 men, who presented at our department with a fever higher than 38.3 degrees C, were randomly selected. We investigated the fraction of patients who had serum PSA levels higher than 4.0 ng/ml and categorized them according to an initial diagnosis of pyelonephritis, ABP, other urogenital infections, and fever of unknown origin (FUO). RESULTS: Six of nine cases initially diagnosed as pyelonephritis, presented with elevated PSA levels between 9.5 and 75.1 ng/ml. All six cases of clinically diagnosed prostatitis had PSA elevated between 4.1 and 13.6 ng/ml. In 8 of 18 FUO cases, PSA was elevated between 5.1 and 77.0 ng/ml. PSA levels significantly correlated with age (P < 0.005). All 20 patients with elevated PSA received antibiotics, and serum PSA was significantly reduced in all cases (P < 0.001) together with the alleviation of fever and normalization of CRP. CONCLUSIONS: PSA is a prompt and steady diagnostic tool for identifying ABP that might be missed or misdiagnosed. We recommend the measurement of PSA in cases not only with urologic infection but also puzzling pyrexia.


Assuntos
Antígeno Prostático Específico/sangue , Prostatite/diagnóstico , Prostatite/microbiologia , Pielonefrite/diagnóstico , Doença Aguda , Adulto , Idoso , Infecções Bacterianas , Erros de Diagnóstico , Febre de Causa Desconhecida , Humanos , Masculino , Pessoa de Meia-Idade , Reprodutibilidade dos Testes , Sensibilidade e Especificidade
3.
Nihon Igaku Hoshasen Gakkai Zasshi ; 63(6): 311-5, 2003 Jul.
Artigo em Japonês | MEDLINE | ID: mdl-12934549

RESUMO

OBJECTIVE: To clarify the high-resolution CT(HRCT) findings of pulmonary atypical adenomatous hyperplasia (AAH) of 5 mm or less in diameter. MATERIALS AND METHODS: We evaluated the HRCT findings of 43 histopathologically confirmed AAH of 5 mm or less in diameter in 7 patients who underwent lobectomy for pulmonary adenocarcinoma. For comparison, we also examined the HRCT findings of 13 bronchioloalveolar carcinomas (BAC) of the same size from these patients. RESULTS: We identified 36 of 43 AAH and all 13 BAC on HRCT performed with multidetector-row CT. Thirty-five AAH and 11 BAC showed ground-glass opacity without any high-attenuation component. Margins of 20 AAH were well defined, and 16 were ill defined. In BAC, 11 lesions demonstrated well-defined margins, with only 2 showing ill-defined margins. CONCLUSION: Most AAH lesions of 5 mm or less in diameter are identified as ground-glass opacity on HRCT. Detection of minute ground-glass opacity is important in locating AAH on HRCT.


Assuntos
Adenocarcinoma Bronquioloalveolar/diagnóstico por imagem , Adenomatose Pulmonar/diagnóstico por imagem , Adenomatose Pulmonar/patologia , Neoplasias Pulmonares/diagnóstico por imagem , Neoplasias Pulmonares/patologia , Tomografia Computadorizada por Raios X , Adenocarcinoma Bronquioloalveolar/patologia , Idoso , Feminino , Humanos , Hiperplasia/diagnóstico por imagem , Hiperplasia/patologia , Masculino , Pessoa de Meia-Idade , Lesões Pré-Cancerosas/diagnóstico por imagem , Intensificação de Imagem Radiográfica
4.
Pathol Int ; 52(5-6): 416-22, 2002.
Artigo em Inglês | MEDLINE | ID: mdl-12100526

RESUMO

The case of a 70-year-old man with a hitherto undescribed pleural mesothelioma is reported. The tumor was localized in the left lung apex and had invaded the parietal pleura. Histologically, the tumor was characterized by a proliferation of epithelioid cells and the formation of microcysts. The tumor cells were positive for calretinin and vimentin, and possessed abundant microvilli, indicating a mesothelial cell origin for the tumor. A high Ki-67 index and mitotic index, and the recurrence of the tumor after surgery, indicated malignancy. Based on the evidence, we propose that the tumor is a microcystic variant of a localized malignant mesothelioma.


Assuntos
Tumor Adenomatoide/patologia , Mesotelioma Cístico/metabolismo , Mesotelioma Cístico/patologia , Neoplasias Pleurais/metabolismo , Neoplasias Pleurais/patologia , Adenocarcinoma/patologia , Idoso , Diagnóstico Diferencial , Humanos , Imuno-Histoquímica , Masculino , Mesotelioma Cístico/ultraestrutura , Microscopia Eletrônica , Neoplasias Primárias Múltiplas , Segunda Neoplasia Primária , Neoplasias Pleurais/ultraestrutura
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