Publications by authors named "T Uryu"

Article Synopsis
  • Pulmonary veno-occlusive disease (PVOD) is a very rare condition that leads to pulmonary hypertension.
  • Previous studies have identified specific CT scan features of PVOD, such as centrilobular ground-glass opacities and a mosaic pattern.
  • This text mentions a unique observation where chest CT scans showed that pulmonary consolidation disappeared when the patient was repositioned, which hasn't been reported before.
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Epidermal growth factor receptor-tyrosine kinase inhibitor (EGFR-TKI)-targeted therapy has emerged as a viable treatment for patients with advanced non-small cell lung cancer with common EGFR mutations. The uncommon G719X and S768I mutations can co-occur as complex mutations in the same tumor. Here we report a case of a 72-year-old male patient with double lung carcinoma, with G719X and S768I complex mutations detected in the right upper lung lobe along with brain metastases.

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A 69-year-old Japanese man visited our hospital because of worsening shortness of breath. His chest computed tomography (CT) showed a giant left lung mass with a massive left pleural effusion. He could not be treated with chemotherapy and eventually died from a rapidly progressive tumor.

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Introduction: We conducted a drug use investigation to investigate the safety and efficacy of tigecycline, which has been approved for clinical use for the treatment of multidrug-resistant gram-negative infections in Japan.

Methods: This was an open-label, observational, multicenter cohort study that included all patients who received tigecycline.

Results: A total of 116 patients were registered between December 2012 and April 2016 and all of them were evaluated for safety and efficacy.

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Objective: A prospective, observational, post-marketing surveillance was conducted to assess the safety and effectiveness of temsirolimus in patients with renal cell carcinoma in Japan.

Methods: Patients prescribed temsirolimus for advanced renal cell carcinoma were registered and received temsirolimus (25 mg weekly, intravenous infusion for 30-60 minutes) in routine clinical settings (observation period: 96 weeks).

Results: Among 1001 patients included in the safety analysis data set (median age, 65.

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