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1.
Pediatr Radiol ; 28(9): 711-3, 1998 Sep.
Article in English | MEDLINE | ID: mdl-9732502

ABSTRACT

We report two infants with eosinophilic gastroenteritis (EG). This rare disease can mimic the clinical symptoms and US appearance of idiopathic hypertrophic pyloric stenosis (IHPS). US examination of the antropyloric region with a high-frequency linear transducer can assist in the differentiation of EG from IHPS, which is important because the therapeutic approaches are completely different. Eosinophilic gastroenteritis should be considered in the differential diagnosis of IHPS, especially when there has been an ineffective pyloromyotomy.


Subject(s)
Eosinophilia/diagnostic imaging , Gastroenteritis/diagnostic imaging , Pyloric Stenosis/diagnostic imaging , Adrenal Cortex Hormones/therapeutic use , Diagnosis, Differential , Eosinophilia/complications , Eosinophilia/drug therapy , Female , Gastroenteritis/complications , Gastroenteritis/drug therapy , Humans , Infant , Infant, Newborn , Ultrasonography , Vomiting/etiology
2.
Clin Radiol ; 51(3): 167-9, 1996 Mar.
Article in English | MEDLINE | ID: mdl-8605745

ABSTRACT

Fifty-seven sonograms of 18 children with Hashimoto thyroiditis were retrospectively assessed. Thirty-three examinations (in 12 patients) showed thyroid glands which were more reflective than adjacent strap muscles, 22 studies (in eight patients) demonstrated glands of equal reflectivity and two examinations (in one child) depicted thyroid glands of lower reflectivity than muscle. The most frequent ultrasound appearance consisted of 2-5 mm echopenic lesions generally distributed throughout large poorly-defined hyperreflective glands. In serial examinations no correlation was found between laboratory indexes of thyroid status and sonographic findings.


Subject(s)
Thyroid Gland/diagnostic imaging , Thyroiditis, Autoimmune/diagnostic imaging , Child , Female , Humans , Male , Retrospective Studies , Ultrasonography
3.
Pediatr Radiol ; 25 Suppl 1: S150-6, 1995 Nov.
Article in English | MEDLINE | ID: mdl-8577511

ABSTRACT

Heterotaxy is a rare congenital disorder characterised by abnormal viscero-vascular situs with either left or right isomerism that usually coincides with complex cardiac malformation. A precise diagnosis must be made for the selection of the most appropriate treatment. The diagnosis and evaluation of these conditions have been dependent on invasive studies such as angiocardiography, although more recently magnetic resonance imaging (MRI) has been advocated. In paediatric patients MRI is far from ideal because of the need for sedation and monitoring during the examination. The authors reviewed the modalities used in the evaluation of heterotaxy with emphasis on the use of ultrasonography, including pulse and colour flow Doppler imaging. A series of 14 children with heterotaxy is presented; ten with left abdominal isomerism (polysplenia) and four with right isomerism (asplenia). Results of abdominal sonography were compared with those of echo- and angiocardiography, surgery and autopsy. Of the ten children with left abdominal isomerism, two had no cardiac abnormalities. All those with right isomerism had a complex vitium. One patient with left abdominal isomerism proved to have right atrial isomerism. Some new reproducible patterns in viscero-vascular derangement are reported. The predictable patterns of left and right isomerism are outlined and atypical features discussed.


Subject(s)
Abnormalities, Multiple/diagnostic imaging , Abnormalities, Multiple/diagnosis , Child , Child, Preschool , Diagnostic Imaging , Female , Heart Defects, Congenital/diagnostic imaging , Humans , Infant , Infant, Newborn , Male , Situs Inversus/diagnostic imaging , Spleen/abnormalities , Syndrome , Ultrasonography, Doppler, Color
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