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The Journal of Bone & Joint Surgery British Volume
Vol. 87-B, Issue 2 | Pages 279 - 279
1 Feb 2005
Bennet G


The Journal of Bone & Joint Surgery British Volume
Vol. 76-B, Issue 5 | Pages 814 - 817
1 Sep 1994
Craigen M Bennet G MacKenzie Reid R

We reviewed the records and radiographs of seven children who presented with knee pain, local tenderness over the medial femoral condyle, and radiological irregularity of the distal medial metaphysis of the femur suggestive of malignancy. In the five patients who had biopsies, histological changes were consistent with musculotendinous avulsion, and the dissection of ten cadavers confirmed the site to be the insertion of part of the adductor magnus. The recognition of this lesion and knowledge of its benign nature may avoid unnecessary anxiety and needless biopsy.


The Journal of Bone & Joint Surgery British Volume
Vol. 74-B, Issue 6 | Pages 906 - 909
1 Nov 1992
Wang E Simpson S Bennet G

We reviewed 52 cases of osteomyelitis of the calcaneum. The clinical symptoms and signs were well defined, but different and less dramatic than those of long-bone osteomyelitis. Blood cultures were positive in 41% of cases and tissue cultures in 91%. Routine haematological tests were of little value, and radiological changes were often delayed, and were absent in 12%. With early diagnosis, treatment with antibiotics alone was usually effective, but complications and chronic disease were more likely if there was delay. Early diagnosis is the key to successful treatment. We describe a new physical sign and consider that diagnosis is almost always possible by clinical methods.


The Journal of Bone & Joint Surgery British Volume
Vol. 74-B, Issue 5 | Pages 643 - 644
1 Sep 1992
Bennet G


The Journal of Bone & Joint Surgery British Volume
Vol. 71-B, Issue 1 | Pages 30 - 32
1 Jan 1989
Roberts J Bennet G MacKenzie

We report five examples of physeal widening in four children with myelomeningocele. In all cases there was rapid clinical resolution with the use of the patients' normal orthoses and minor limitation of activity, and there was no evidence of early epiphyseal closure or growth disturbance. We suggest that recognition of the pathological process before fracture occurred may explain the rapid return to normal.


The Journal of Bone & Joint Surgery British Volume
Vol. 64-B, Issue 3 | Pages 289 - 294
1 Jun 1982
Bennet G Rang M Roye D Aprin H

Almost one child in twenty with trisomy 21 will develop spontaneous dislocation of the hip between learning to walk and the age of 10 years. After the age of two years spontaneous habitual dislocation may occur. If left untreated, acute dislocation, subluxation and fixed dislocation follow in sequence. The natural history of the condition is described and the clinical and radiological features of 45 dislocations in 28 patients are presented. Nineteen had received no treatment. The most effective treatment was found to be pelvic or femoral osteotomy, combined with capsular plication, carried out in the phase of habitual dislocation. Once subluxation or fixed dislocation was present, the results of operation were poor and it is not recommended. All patients, even if left untreated, remain mobile. Pain is not a prominent feature.