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Biomedical subjects

P Rigault

Publications and source records attributed to P Rigault.

At least 181 records · Page 10Linked to original sources

[Hemivertebra. -- classification, natural history and prognosis (author's transl)].

The authors have studied a series of seventy patients with hemivertebra. Classification should be based on two criteria--firstly, that the hemivertebra can be fused or separate and secondly, vertebrae above and below the hemivertebra may or may not show transitional abnormality. The natural history may take one of three courses: 1--Deformity may be severe from the beginning in cases of separate hemivertebra associated with transitional abnormalites. 2--The deformity may be stable until the age of nine or ten years, after which a severe scoliosis or kypho-scoliosis may develop. 3--The deformity may be stable throughout the whole of the growing period. The prognosis should be based on the existence of transitional abnormalities, the characteristics of the hemisvertebra (separate or fused), the sex of the patient, assoicated congenital defects, the rotation of the hemivertebra, and the level of the deformity. Treatment should be surgical in cases with early progression during the first few years of life by excision of the hemisvertebra associated with correction using Harrington rods. At the thoracic level, this surgical procedure is dangerous and spine fusion is more appropriate. The second period for surgical treatment is at puberty, either by spine fusion or correction and fusion. At this age, excision of the hemivertebra may still be indicated in the lumbar spine.

Adolescent↗

[Progressive femoral lengthening in children. Apropos of 36 cases].

The authors have analysed the result of femoral lengthening in 36 cases, 24 of them congenital. The technique, which is fully described, was that of progressive lengthening using external distraction either by the Judet or Wagner method. The average lengthening obtained was 18,3 p. 100 of the initial length of the femur--that is 5.2 centimetres on average. The bony and articular complications are described. The authors believe that, thanks to modifications of their technique, one femur should normally be able to be lengthened by 20 to 25 p. 100 in 30 days and should be solid in six months.

Adolescent↗

[Diastematomelia (author's transl)].

21 cases have been observed and followed up for 10 years. All were children. Three types of anomaly were noted: Spinal curvature (mostly scoliosis), skin abnormalities in the mid line (hypertrichosis, angioma, skin dimples) and problems in the lower limbs (varus deformities of the feet, leg length discrepancy, muscular atrophy, neurological disorders). These signs, even if not all are present, must lead to a study of the vertebral bodies and to gas myelography whcih demonstrates a double spinal cord over a variable length from 2 to 14 segments. 15 children were treated surgically by mobilisation of the spinal cord and arthrodesis of the spine. 4 of them were made worse. In contrast, none of the 6 children treated conservately was made worse. The authors conclude that surgery should be reserved for recent spontaneous neurological deterioration and severe deformities of the spine.

Adolescent↗