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1.
AJNR Am J Neuroradiol ; 41(4): 725-728, 2020 04.
Artículo en Inglés | MEDLINE | ID: mdl-32193189

RESUMEN

BACKGROUND AND PURPOSE: In the medicolegal literature, notching of the corpus callosum has been reported to be associated with fetal alcohol spectrum disorders. Our purpose was to analyze the prevalence of notching of the corpus callosum in a fetal alcohol spectrum disorders group and a healthy population to determine whether notching occurs with increased frequency in the fetal alcohol spectrum disorders population. MATERIALS AND METHODS: We performed a multicenter search for cases of fetal alcohol spectrum disorders and included all patients who had a sagittal T1-weighted brain MR imaging. Patients with concomitant intracranial pathology were excluded. The corpus callosum was examined for notches using previously published methods. A χ2 test was used to compare the fetal alcohol spectrum disorders and healthy groups. RESULTS: Thirty-three of 59 patients with fetal alcohol spectrum disorders (0-44 years of age) identified across all centers had corpus callosum notching. Of these, 8 had an anterior corpus callosum notch (prevalence, 13.6%), 23 had a posterior corpus callosum notch (prevalence, 39%), and 2 patients demonstrated undulated morphology (prevalence, 3.4%). In the healthy population, the anterior notch prevalence was 139/875 (15.8%), posterior notch prevalence was 378/875 (43.2%), and undulating prevalence was 37/875 (4.2%). There was no significant difference among the anterior (P = .635), posterior (P = .526), and undulating (P = .755) notch prevalence in the fetal alcohol spectrum disorders and healthy groups. CONCLUSIONS: There was no significant difference in notching of the corpus callosum between patients with fetal alcohol spectrum disorders and the healthy population. Although reported to be a marker of fetal alcohol spectrum disorders, notching of the corpus callosum should not be viewed as a specific finding associated with fetal alcohol spectrum disorders.


Asunto(s)
Cuerpo Calloso/diagnóstico por imagen , Trastornos del Espectro Alcohólico Fetal/diagnóstico por imagen , Adolescente , Adulto , Niño , Preescolar , Cuerpo Calloso/patología , Femenino , Trastornos del Espectro Alcohólico Fetal/patología , Humanos , Lactante , Recién Nacido , Imagen por Resonancia Magnética/métodos , Masculino , Neuroimagen/métodos , Embarazo , Adulto Joven
2.
AJNR Am J Neuroradiol ; 40(5): 866-871, 2019 05.
Artículo en Inglés | MEDLINE | ID: mdl-30975652

RESUMEN

BACKGROUND AND PURPOSE: Noncontrast CT of the head is the initial imaging test for traumatic brain injury, stroke, or suspected nonaccidental trauma. Low-dose head CT protocols using filtered back-projection are susceptible to increased noise and decreased image quality. Iterative reconstruction noise suppression allows the use of lower-dose techniques with maintained image quality. We review our experience with children undergoing emergency head CT examinations reconstructed using knowledge-based iterative model reconstruction versus standard filtered back-projection, comparing reconstruction times, radiation dose, and objective and subjective image quality. MATERIALS AND METHODS: This was a retrospective study comparing 173 children scanned using standard age-based noncontrast head CT protocols reconstructed with filtered back-projection with 190 children scanned using low-dose protocols reconstructed with iterative model reconstruction. ROIs placed on the frontal white matter and thalamus yielded signal-to-noise and contrast-to-noise ratios. Volume CT dose index and study reconstruction times were recorded. Random subgroups of patients were selected for subjective image-quality review. RESULTS: The volume CT dose index was significantly reduced in studies reconstructed with iterative model reconstruction compared with filtered back-projection, (mean, 24.4 ± 3.1 mGy versus 31.1 ± 6.0 mGy, P < .001), while the SNR and contrast-to-noise ratios improved 2-fold (P < .001). Radiologists graded iterative model reconstruction images as superior to filtered back-projection images for gray-white matter differentiation and anatomic detail (P < .001). The average reconstruction time of the filtered back-projection studies was 101 seconds, and with iterative model reconstruction, it was 147 seconds (P < .001), without a practical effect on work flow. CONCLUSIONS: In children referred for emergency noncontrast head CT, optimized low-dose protocols with iterative model reconstruction allowed us to significantly reduce the relative dose, on average, 22% compared with filtered back-projection, with significantly improved objective and subjective image quality.


Asunto(s)
Lesiones Traumáticas del Encéfalo/diagnóstico por imagen , Cabeza/diagnóstico por imagen , Neuroimagen/métodos , Interpretación de Imagen Radiográfica Asistida por Computador/métodos , Tomografía Computarizada por Rayos X/métodos , Adolescente , Niño , Femenino , Humanos , Masculino , Dosis de Radiación , Estudios Retrospectivos
3.
Genes Immun ; 11(5): 374-83, 2010 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-20535134

RESUMEN

Congenital Toxoplasma gondii infection can result in intracranial calcification, hydrocephalus and retinochoroiditis. Acquired infection is commonly associated with ocular disease. Pathology is characterized by strong proinflammatory responses. Ligation of ATP by purinergic receptor P2X(7), encoded by P2RX7, stimulates proinflammatory cytokines and can lead directly to killing of intracellular pathogens. To determine whether P2X(7) has a role in susceptibility to congenital toxoplasmosis, we examined polymorphisms at P2RX7 in 149 child/parent trios from North America. We found association (FBAT Z-scores +/-2.429; P=0.015) between the derived C(+)G(-) allele (f=0.68; OR=2.06; 95% CI: 1.14-3.75) at single-nucleotide polymorphism (SNP) rs1718119 (1068T>C; Thr-348-Ala), and a second synonymous variant rs1621388 in linkage disequilibrium with it, and clinical signs of disease per se. Analysis of clinical subgroups showed no association with hydrocephalus, with effect sizes for associations with retinal disease and brain calcifications enhanced (OR=3.0-4.25; 0.004

Asunto(s)
Coriorretinitis/genética , Predisposición Genética a la Enfermedad/genética , Receptores Purinérgicos P2/genética , Toxoplasmosis Congénita/genética , Adulto , Brasil , Preescolar , Coriorretinitis/etiología , Femenino , Estudio de Asociación del Genoma Completo , Haplotipos/genética , Humanos , Patrón de Herencia/genética , Desequilibrio de Ligamiento , Modelos Logísticos , Masculino , América del Norte , Polimorfismo de Nucleótido Simple/genética , Receptores Purinérgicos P2X7 , Toxoplasmosis Congénita/complicaciones
4.
AJNR Am J Neuroradiol ; 28(6): 1133-8, 2007.
Artículo en Inglés | MEDLINE | ID: mdl-17569973

RESUMEN

BACKGROUND AND PURPOSE: The size of vestibular aqueducts (VAs) seen on CT studies varies. The current practice of calling a VA enlarged when it exceeds a certain threshold (eg, 1.5 mm at the midpoint) is arbitrary. Our hypothesis was that statistical analysis of the range of VA widths in a normal-hearing population would lead to a mathematic definition of the upper-limit-of-normal VA width. MATERIALS AND METHODS: The VA midpoint and opercular widths were measured in 73 children with normal hearing. Statistical analysis yielded values of the 99 th, 97.5th, 95th, 90th, 75th, and 50th percentiles for this normal distribution. RESULTS: The upper-limit-of-normal (95th percentile) values for the VA midpoint and opercular widths were 0.9 and 1.9 mm, respectively. The VAs with greater widths may reasonably be considered enlarged. CONCLUSION: The VAs with midpoint or opercular widths of 1.0 and 2.0 mm or greater, respectively, are enlarged.


Asunto(s)
Antropometría/métodos , Modelos Anatómicos , Modelos Neurológicos , Tamaño de los Órganos/fisiología , Acueducto Vestibular/anatomía & histología , Acueducto Vestibular/diagnóstico por imagen , Niño , Simulación por Computador , Interpretación Estadística de Datos , Femenino , Humanos , Masculino , Modelos Estadísticos , Distribución Normal , Radiografía , Reproducibilidad de los Resultados , Sensibilidad y Especificidad
5.
Pediatr Radiol ; 31(6): 403-5, 2001 Jun.
Artículo en Inglés | MEDLINE | ID: mdl-11436886

RESUMEN

Desmoplastic infantile ganglioglioma (DIG) is a rare brain tumor encountered in infants. In spite of its large size at presentation and occasional high mitotic activity on histopathology, the tumor has a good prognosis. A 7-month-old baby girl developed increasing head circumference. On ultrasound, a large multicystic mass was seen. We report the cranial ultrasound findings for the first time. Correlative imaging of this recently recognized entity is shown.


Asunto(s)
Neoplasias Encefálicas/diagnóstico por imagen , Ganglioglioma/diagnóstico por imagen , Neoplasias Encefálicas/patología , Femenino , Ganglioglioma/patología , Humanos , Lactante , Ultrasonografía
6.
Radiographics ; 21(3): 705-17, 2001.
Artículo en Inglés | MEDLINE | ID: mdl-11353117

RESUMEN

Hypoplastic left heart syndrome (HLHS) is a complex combination of cardiac malformations that probably results from multiple developmental errors in the early stages of cardiogenesis and that, if left untreated, invariably proves fatal. A variety of chest radiographic findings are seen in patients with HLHS, including an enlarged cardiac silhouette (notably a prominent right atrium), pulmonary venous hypertension, an atrial septal defect, and valvular stenosis or atresia. The recent evolution of palliative surgical procedures (modified Norwood procedure, bidirectional cavopulmonary shunt, modified Fontan procedure, aortic valvuloplasty, heart transplantation) has increased the survival rate in children with HLHS. Echocardiography allows accurate assessment of the size and location of the ductus arteriosus, the hemodynamics of the aortic root, the patency and size of the foramen ovale or atrial septal defect, and the presence of a ventricular septal defect to help determine whether surgical intervention is appropriate and, if so, to facilitate planning. Pediatric radiologists now view radiologic images obtained in patients with HLHS before surgical intervention and at important intervals during treatment. Familiarity with the malformations that characterize HLHS and the surgical procedures used to enhance postnatal survival will help pediatric radiologists provide better care for patients with this relatively common pathologic condition.


Asunto(s)
Síndrome del Corazón Izquierdo Hipoplásico/diagnóstico , Angiografía Coronaria , Circulación Coronaria , Ecocardiografía , Humanos , Síndrome del Corazón Izquierdo Hipoplásico/embriología , Síndrome del Corazón Izquierdo Hipoplásico/cirugía , Recién Nacido , Imagen por Resonancia Magnética , Radiografía Torácica , Ultrasonografía Prenatal
7.
Pediatr Radiol ; 29(7): 530-5, 1999 Jul.
Artículo en Inglés | MEDLINE | ID: mdl-10398791

RESUMEN

BACKGROUND: Pneumatosis intestinalis (PI) represents gas in the bowel wall. The appearance of PI using high-resolution ultrasound (HRUS) has not been well described. OBJECTIVE: The purpose of this report is to describe a new ultrasound sign of pneumatosis seen in three patients. This sign, called the "circle sign", is indicative of bubbles of gas within the circumference of the bowel, producing an appearance of a continuous echogenic ring on ultrasound. Further studies of the sonographic characteristics of pneumatosis were performed with an in vitro model. MATERIALS AND METHODS: HRUS was performed prospectively in three patients demonstrating extensive PI radiographically. The appearance of the gas was characterized and the behavior of the intramural bubbles was studied when the bowel was compressed with the ultrasound transducer. Either CT scan or pathologic correlation was obtained in all patients. Experimental models of PI using air injected into the wall of sausage casing were developed. RESULTS: The presence of echogenic gas bubbles within the circumference of the wall of the bowel seen with HRUS was shown to represent pneumatosis intestinalis at histologic examination or by CT scanning in the three study patients. In vitro studies confirmed the clinical impression that the use of compression is helpful in distinguishing intramural from intraluminal air. CONCLUSION: The presence of echogenic gas bubbles in the wall of the bowel, often seen as a circle within the circumference of the bowel, may be helpful in diagnosing PI on ultrasound using HRUS.


Asunto(s)
Neumatosis Cistoide Intestinal/diagnóstico por imagen , Adolescente , Niño , Humanos , Recién Nacido , Masculino , Estudios Prospectivos , Tomografía Computarizada por Rayos X , Ultrasonografía
8.
J Clin Ultrasound ; 26(9): 470-3, 1998.
Artículo en Inglés | MEDLINE | ID: mdl-9800162

RESUMEN

We report an unusual case of superficial venous thrombosis in a cyanotic 12-year-old child who had undergone recent appendectomy. Although compression, color Doppler, and duplex ultrasound techniques remain the keys to the diagnosis of venous thrombosis, SieScape sonography was beneficial in demonstrating the extent of the thrombi and their location along a superficial thrombosed vein.


Asunto(s)
Linfadenitis/complicaciones , Quiste Poplíteo/diagnóstico por imagen , Vena Poplítea/diagnóstico por imagen , Ultrasonografía Doppler , Trombosis de la Vena/diagnóstico por imagen , Enfermedad Aguda , Velocidad del Flujo Sanguíneo , Niño , Diagnóstico Diferencial , Complejo de Eisenmenger/complicaciones , Femenino , Estudios de Seguimiento , Humanos , Pierna/irrigación sanguínea , Linfadenitis/diagnóstico por imagen , Linfadenitis/patología , Angiografía por Resonancia Magnética , Quiste Poplíteo/complicaciones , Quiste Poplíteo/patología , Vena Poplítea/patología , Trombosis de la Vena/complicaciones , Trombosis de la Vena/cirugía
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