Asunto(s)
Dermatosis Facial/diagnóstico , Enfermedades del Cabello/diagnóstico , Inmunosupresores/efectos adversos , Trasplante de Riñón/efectos adversos , Infecciones por Polyomavirus/diagnóstico , Biopsia , Cidofovir/administración & dosificación , Dermatosis Facial/tratamiento farmacológico , Dermatosis Facial/inmunología , Dermatosis Facial/virología , Femenino , Rechazo de Injerto/inmunología , Rechazo de Injerto/prevención & control , Enfermedades del Cabello/tratamiento farmacológico , Enfermedades del Cabello/inmunología , Enfermedades del Cabello/virología , Folículo Piloso/inmunología , Folículo Piloso/patología , Folículo Piloso/virología , Humanos , Huésped Inmunocomprometido , Persona de Mediana Edad , Poliomavirus/inmunología , Poliomavirus/aislamiento & purificación , Infecciones por Polyomavirus/tratamiento farmacológico , Infecciones por Polyomavirus/inmunología , Infecciones por Polyomavirus/virología , Piel/inmunología , Piel/patología , Piel/virología , Crema para la Piel/administración & dosificaciónRESUMEN
IMPORTANCE: The Zika virus epidemic has been declared a public health emergency of international concern by the World Health Organization. We describe the mucocutaneous features and histologic correlation in a patient with the acute Zika virus infection. OBSERVATIONS: We observed the presence of a diffuse papular descending eruption, petechiae on the palate, and hyperemic sclerae in a 44-year-old man returning from Puerto Rico with confirmatory testing for the Zika virus. CONCLUSIONS AND RELEVANCE: A detailed awareness of mucocutaneous findings associated with Zika virus infection will support its early recognition and will facilitate elimination of Zika infection from consideration for concerned patients who present with other, more common erythematous eruptions.
Asunto(s)
Membrana Mucosa/patología , Enfermedades Cutáneas Virales/patología , Infección por el Virus Zika/patología , Enfermedad Aguda , Adulto , Humanos , Hiperemia/virología , Masculino , Membrana Mucosa/virología , Puerto Rico , Púrpura/virología , Esclerótica/patología , ViajeRESUMEN
INTRODUCTION: Multiple scoring systems have been proposed for prostate MRI reporting. We sought to review the clinical impact of the new Prostate Imaging Reporting and Data System v2 (PI-RADS) and compare those results to our proposed Simplified Qualitative System (SQS) score with respect to detection of prostate cancers and clinically significant prostate cancers. METHODS: All patients who underwent multiparametric prostate MRI (mpMRI) had their images interpreted using PI-RADS v1 and SQS score. PI-RADS v2 was calculated from prospectively collected data points. Patients with positive mpMRIs were then referred by their urologists for enrollment in an IRB-approved prospective phase III trial of mpMRI-Ultrasound (MR/TRUS) fusion biopsy of suspicious lesions. Standard 12-core biopsy was performed at the same setting. Clinical data were collected prospectively. RESULTS: 1060 patients were imaged using mpMRI at our institution during the study period. 341 participants were then referred to the trial. 312 participants underwent MR/TRUS fusion biopsy of 452 lesions and were included in the analysis. 202 participants had biopsy-proven cancer (64.7%) and 206 (45.6%) lesions were positive for cancer. Distribution of cancer detected at each score produced a Gaussian distribution for SQS while PI-RADS demonstrates a negatively skewed curve with 82.1% of cases being scored as a 4 or 5. Patient-level data demonstrated AUC of 0.702 (95% CI 0.65 to 0.73) for PI-RADS and 0.762 (95% CI 0.72 to 0.81) for SQS (p< 0.0001) with respect to the detection of prostate cancer. The analysis for clinically significant prostate cancer at a per lesion level resulted in an AUC of 0.725 (95% CI 0.69 to 0.76) and 0.829 (95% CI 0.79 to 0.87) for the PI-RADS and SQS score, respectively (p< 0.0001). CONCLUSIONS: mpMRI is a useful tool in the workup of patients at risk for prostate cancer, and serves as a platform to guide further evaluation with MR/TRUS fusion biopsy. SQS score provided a more normal distribution of scores and yielded a higher AUC than PI-RADS v2. However until our findings are validated, we recommend reporting of detailed sequence-specific findings. This will allow for prospectively collected data to be utilized in determining the impact of ongoing changes to these scoring systems as our understanding of mpMRI interpretation evolves.