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S Jéquier

Publications and source records attributed to S Jéquier.

13 recordsLinked to original sources

Ultrasonography of jejunal intussusception in children.

OBJECTIVE: To describe the ultrasonographic findings in different forms of jejunal intussusception in three children. PATIENTS AND METHOD: Two children with hamartomatous polyps of the jejunum acting as lead points for antegrade jejunoileocolic intussusception and retrograde jejunoduodenogastric intussusception respectively and one child with idiopathic postoperative intussusception were examined by ultrasonography. RESULTS: The findings of the US studies were abnormal and different in each case, depending on the underlying condition and the direction (antegrade or retrograde) of the intussusception. The hamartomatous polyps were seen as hyperechoic solid masses but could not be diagnosed more specifically with US. A target lesion was found in the case of idiopathic postoperative intussusception. The US results prompted the next imaging procedure, air enema in the one patient in whom the intussusception had reached the colon and preoperative barium meal in all of the patients. Surgery was performed without the delay that usually occurs with jejunal intussusception. CONCLUSION: In the appropriate clinical setting, US should be used to look for jejunal intussusception, so that suitable diagnostic gastrointestinal studies can be performed and delay in diagnosis avoided.

Child

Testicular torsion in infants and children: diagnosis with Doppler sonography.

The accuracy of Doppler sonography in the evaluation of testicular torsion was tested in 65 boys (aged 0-18 years) with acute scrotal pain or swelling. All patients underwent pulsed Doppler sonography of both testes, followed by scintigraphy (n = 16) and/or surgery (n = 34) and a close clinical follow-up for 4-8 months (n = 31). Color Doppler sonography was performed in 29 patients. The testicular artery was deemed patent if Doppler shifts from branches within the parenchyma could be found. Surgery revealed 19 cases of testicular torsion, 17 of which were diagnosed with Doppler sonography. There were six technical failures, in which no signals could be found on either side. In four boys, no color signals were obtained in either testis but subsequent examination with a mechanical sector scanner and pulsed Doppler sonography yielded arterial signals. Doppler sonography was successful in 59 of 65 boys (91%) and yielded a sensitivity of 89% and specificity of 100%. Pulsed Doppler sonography with mechanical sector scanners was more sensitive than color Doppler sonography. Intermittent torsion was missed both with Doppler sonography and scintigraphy.

Adolescent

Duplex Doppler sonographic examinations of the testis in prepubertal boys.

This retrospective study of 143 pediatric patients with unilateral acute scrotal disease was done to assess the value of duplex Doppler sonographic examination prior to puberty (110 patients) in comparison to a pubertal group (33 patients) in a pediatric hospital, where the examinations are done by staff radiologists and radiology residents of varying degrees of expertise and experience with Doppler technique. All patients seen during an 18 month period were included. The unaffected side was examined in most patients and served as control. The normal Doppler shift in the center of the prepubertal testis was found to be 0.2 to 0.5 kHz, when using a 5 MHz duplex Doppler probe. With puberty, the Doppler shift increased to 0.5 to 1 kHz. Of 18 patients (10 prepubertal) with testicular torsion, five (three prepubertal) had false-positive Doppler shift. In four of these five cases, faulty placement of the Doppler sample volume cursor was probably the cause. Using a multi-way frequency analysis, puberty was found to have no significant influence on results of Doppler signal (chi square = 0.1346; P = 0.7137). Duplex Doppler sonographic examination is as useful to rule out testicular torsion in prepubertal boys as it is after puberty. Meticulous technique is essential. The opposite side should be examined first and serves as control for the affected one. Results showing no flow in the center of the diseased testis with positive flow in the unaffected one should lead to further clinical action (scintigraphy or surgery).

Adolescent

A new acro-cranio-facial dysostosis syndrome in sisters.

Two sisters born to consanguineous parents had a syndrome of short stature, acrocephaly, hypertelorism, proptosis, ptosis, down-slanting palpebral fissures, high nose bridge and anteverted nares, short philtrum, cleft palate, micrognathia, abnormal external ears, preauricular pits, sensorineural and conductive deafness, proximally placed first toes and digitalized thumbs, bulbous digits, metatarsus adductus, and pectus excavatum. Radiological abnormalities included craniosynostosis, increased mandibular angle and antegonial notching of mandible; hypoplastic first metacarpals and metatarsals; hypoplastic distal phalanges; partial duplication of the distal phalanx of the thumb; malformed malleus and incus; tall lumbar vertebrae, increased interpedicular distance, and posterior scalloping; flared iliac wings, narrow supraacetabular regions, acetabular "dysplasia," and coxa valga. Autosomal recessive inheritance is suggested.

Child, Preschool

[Bone maturity and physical performance].

We have examined the relation between physical performance (as measured with the CAHPER tests), bone age (Greulich and Pyl's wrist evaluation) and dental age (Garn's method). Our study included 164 boys and 149 girls aged from 7 to 11. In spite of interesting significant simple correlation between most of the CAHPER tests and bone age measurements for the pre-pubescent period, the latter remains of negligible value in predicting physical performance in the studied children when variables like chronological age, body height and body weight are already included in the prediction equation.

Age Determination by Skeleton

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Cataract