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1.
J Am Coll Radiol ; 20(11S): S351-S381, 2023 11.
Artículo en Inglés | MEDLINE | ID: mdl-38040460

RESUMEN

Pediatric heart disease is a large and diverse field with an overall prevalence estimated at 6 to 13 per 1,000 live births. This document discusses appropriateness of advanced imaging for a broad range of variants. Diseases covered include tetralogy of Fallot, transposition of great arteries, congenital or acquired pediatric coronary artery abnormality, single ventricle, aortopathy, anomalous pulmonary venous return, aortopathy and aortic coarctation, with indications for advanced imaging spanning the entire natural history of the disease in children and adults, including initial diagnosis, treatment planning, treatment monitoring, and early detection of complications. The American College of Radiology Appropriateness Criteria are evidence-based guidelines for specific clinical conditions that are reviewed annually by a multidisciplinary expert panel. The guideline development and revision process support the systematic analysis of the medical literature from peer reviewed journals. Established methodology principles such as Grading of Recommendations Assessment, Development, and Evaluation or GRADE are adapted to evaluate the evidence. The RAND/UCLA Appropriateness Method User Manual provides the methodology to determine the appropriateness of imaging and treatment procedures for specific clinical scenarios. In those instances where peer reviewed literature is lacking or equivocal, experts may be the primary evidentiary source available to formulate a recommendation.


Asunto(s)
Enfermedad de la Arteria Coronaria , Cardiopatías , Adulto , Niño , Humanos , Diagnóstico Diferencial , Diagnóstico por Imagen/métodos , Sociedades Médicas , Estados Unidos
2.
J Radiol Case Rep ; 12(2): 18-27, 2018 Feb.
Artículo en Inglés | MEDLINE | ID: mdl-29875987

RESUMEN

Large septic pulmonary embolus is a rare finding in right-sided endocarditis. The entity represents a challenging diagnosis due to its variable and nonspecific clinical and radiological presentation and similarities with other conditions. We present a case of a 41 year-old woman who developed a large main pulmonary artery embolus and bilateral cavitary lung nodules in the setting of severe sepsis. Pulmonary artery exploration and clot retrieval ultimately revealed a large septic embolus from Streptococcus mutans native pulmonary valve endocarditis. The diagnosis of septic pulmonary emboli from right-sided endocarditis should be considered in patients with ancillary findings of septic embolic phenomenon, particularly the presence of multifocal cavitary nodules and in the setting of appropriate predisposing factors.


Asunto(s)
Endocarditis Bacteriana/diagnóstico por imagen , Endocarditis Bacteriana/microbiología , Embolia Pulmonar/diagnóstico por imagen , Embolia Pulmonar/microbiología , Válvula Pulmonar/diagnóstico por imagen , Válvula Pulmonar/microbiología , Streptococcus mutans/aislamiento & purificación , Adulto , Angiografía por Tomografía Computarizada , Medios de Contraste , Diagnóstico Diferencial , Femenino , Humanos , Yohexol , Arteria Pulmonar
3.
JCI Insight ; 3(7)2018 04 05.
Artículo en Inglés | MEDLINE | ID: mdl-29618661

RESUMEN

We generated a comprehensive atlas of the immunologic cellular networks within human malignant pleural mesothelioma (MPM) using mass cytometry. Data-driven analyses of these high-resolution single-cell data identified 2 distinct immunologic subtypes of MPM with vastly different cellular composition, activation states, and immunologic function; mass spectrometry demonstrated differential abundance of MHC-I and -II neopeptides directly identified between these subtypes. The clinical relevance of this immunologic subtyping was investigated with a discriminatory molecular signature derived through comparison of the proteomes and transcriptomes of these 2 immunologic MPM subtypes. This molecular signature, representative of a favorable intratumoral cell network, was independently associated with improved survival in MPM and predicted response to immune checkpoint inhibitors in patients with MPM and melanoma. These data additionally suggest a potentially novel mechanism of response to checkpoint blockade: requirement for high measured abundance of neopeptides in the presence of high expression of MHC proteins specific for these neopeptides.


Asunto(s)
Antígenos de Neoplasias/inmunología , Regulación Neoplásica de la Expresión Génica/inmunología , Neoplasias Pulmonares/inmunología , Mesotelioma/inmunología , Neoplasias Pleurales/inmunología , Transcriptoma/inmunología , Antígenos de Neoplasias/genética , Antineoplásicos Inmunológicos/farmacología , Antineoplásicos Inmunológicos/uso terapéutico , Línea Celular Tumoral , Receptores Coestimuladores e Inhibidores de Linfocitos T/antagonistas & inhibidores , Receptores Coestimuladores e Inhibidores de Linfocitos T/inmunología , Regulación Neoplásica de la Expresión Génica/genética , Humanos , Estimación de Kaplan-Meier , Pulmón/patología , Pulmón/cirugía , Neoplasias Pulmonares/genética , Neoplasias Pulmonares/mortalidad , Neoplasias Pulmonares/terapia , Espectrometría de Masas/métodos , Mesotelioma/genética , Mesotelioma/mortalidad , Mesotelioma/terapia , Mesotelioma Maligno , Pleura/patología , Pleura/cirugía , Neoplasias Pleurales/genética , Neoplasias Pleurales/mortalidad , Neoplasias Pleurales/terapia , Pronóstico , Estudios Prospectivos , Proteogenómica/métodos , Estudios Retrospectivos , Análisis de la Célula Individual/métodos , Transcriptoma/genética , Resultado del Tratamiento , Microambiente Tumoral/genética , Microambiente Tumoral/inmunología
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