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1.
Pediatr Radiol ; 44(10): 1318-22, 2014 Oct.
Artigo em Inglês | MEDLINE | ID: mdl-24756252

RESUMO

Systemic lupus erythematosis (SLE) can affect the lungs and pleura, usually manifesting with pleural effusions or diffuse parenchymal disease. A rare manifestation of SLE is shrinking lung syndrome, a severe restrictive respiratory disorder. While pleuropulmonary complications of pediatric SLE are common, shrinking lung syndrome is exceedingly rare in children. We present a case of a 13-year-old girl previously diagnosed with lupus, who developed severe dyspnea on exertion and restrictive pulmonary physiology. Her chest radiographs on presentation demonstrated low lung volumes, and CT showed neither pleural nor parenchymal disease. Fluoroscopy demonstrated poor diaphragmatic excursion. While shrinking lung syndrome is described and studied in adults, there is only sparse reference to shrinking lung syndrome in children.


Assuntos
Dispneia/diagnóstico , Lúpus Eritematoso Sistêmico/diagnóstico por imagem , Pleurisia/diagnóstico por imagem , Síndrome do Desconforto Respiratório do Recém-Nascido/diagnóstico por imagem , Tomografia Computadorizada por Raios X/métodos , Adolescente , Diagnóstico Diferencial , Dispneia/complicações , Feminino , Humanos , Lúpus Eritematoso Sistêmico/complicações , Pleurisia/complicações , Síndrome do Desconforto Respiratório do Recém-Nascido/complicações , Síndrome
2.
AJR Am J Roentgenol ; 201(6): W797-808, 2013 Dec.
Artigo em Inglês | MEDLINE | ID: mdl-24261386

RESUMO

OBJECTIVE: The orbit contains structures from which a wide spectrum of disease can arise. This article focuses on orbital anatomy and a simple compartmental approach to evaluating the orbit on diagnostic imaging. The characteristic findings of key fetal structural diseases and a wide spectrum of pediatric orbital disorders, including inflammatory disorders and developmental lesions, and the differential diagnosis of benign versus malignant masses will be discussed. CONCLUSION: Orbital abnormalities in fetuses may be recognized using ultrasound and MRI. Anophthalmia, hypertelorism, and hypotelorism either may be part of a genetic syndrome or may be related to a developmental abnormality of the fetal skull. In the pediatric population, cross-sectional imaging with CT and MRI offers a means to assess which compartments of the orbit are affected. Aggressive masses have characteristic features and must be evaluated for intracranial extension.


Assuntos
Diagnóstico por Imagem , Órbita/anormalidades , Doenças Orbitárias/diagnóstico , Criança , Pré-Escolar , Feminino , Humanos , Lactente , Recém-Nascido , Órbita/anatomia & histologia , Gravidez
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