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1.
AJNR Am J Neuroradiol ; 41(4): 725-728, 2020 04.
Article in English | MEDLINE | ID: mdl-32193189

ABSTRACT

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.


Subject(s)
Corpus Callosum/diagnostic imaging , Fetal Alcohol Spectrum Disorders/diagnostic imaging , Adolescent , Adult , Child , Child, Preschool , Corpus Callosum/pathology , Female , Fetal Alcohol Spectrum Disorders/pathology , Humans , Infant , Infant, Newborn , Magnetic Resonance Imaging/methods , Male , Neuroimaging/methods , Pregnancy , Young Adult
2.
AJNR Am J Neuroradiol ; 40(5): 866-871, 2019 05.
Article in English | MEDLINE | ID: mdl-30975652

ABSTRACT

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.


Subject(s)
Brain Injuries, Traumatic/diagnostic imaging , Head/diagnostic imaging , Neuroimaging/methods , Radiographic Image Interpretation, Computer-Assisted/methods , Tomography, X-Ray Computed/methods , Adolescent , Child , Female , Humans , Male , Radiation Dosage , Retrospective Studies
3.
AJNR Am J Neuroradiol ; 28(6): 1133-8, 2007.
Article in English | MEDLINE | ID: mdl-17569973

ABSTRACT

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.


Subject(s)
Anthropometry/methods , Models, Anatomic , Models, Neurological , Organ Size/physiology , Vestibular Aqueduct/anatomy & histology , Vestibular Aqueduct/diagnostic imaging , Child , Computer Simulation , Data Interpretation, Statistical , Female , Humans , Male , Models, Statistical , Normal Distribution , Radiography , Reproducibility of Results , Sensitivity and Specificity
4.
Radiographics ; 21(3): 705-17, 2001.
Article in English | MEDLINE | ID: mdl-11353117

ABSTRACT

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.


Subject(s)
Hypoplastic Left Heart Syndrome/diagnosis , Coronary Angiography , Coronary Circulation , Echocardiography , Humans , Hypoplastic Left Heart Syndrome/embryology , Hypoplastic Left Heart Syndrome/surgery , Infant, Newborn , Magnetic Resonance Imaging , Radiography, Thoracic , Ultrasonography, Prenatal
5.
J Clin Ultrasound ; 26(9): 470-3, 1998.
Article in English | MEDLINE | ID: mdl-9800162

ABSTRACT

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.


Subject(s)
Lymphadenitis/complications , Popliteal Cyst/diagnostic imaging , Popliteal Vein/diagnostic imaging , Ultrasonography, Doppler , Venous Thrombosis/diagnostic imaging , Acute Disease , Blood Flow Velocity , Child , Diagnosis, Differential , Eisenmenger Complex/complications , Female , Follow-Up Studies , Humans , Leg/blood supply , Lymphadenitis/diagnostic imaging , Lymphadenitis/pathology , Magnetic Resonance Angiography , Popliteal Cyst/complications , Popliteal Cyst/pathology , Popliteal Vein/pathology , Venous Thrombosis/complications , Venous Thrombosis/surgery
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