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The Journal of Bone & Joint Surgery British Volume
Vol. 56-B, Issue 2 | Pages 279 - 290
1 May 1974
Byers PD

1. Osteotomy for osteoarthritis of the hip induces a fibrin layer over the exposed bone which forms the basis of a fibrocellular protective mantle that can differentiate towards cartilage. 2. The process is accompanied by bone remodelling, which reduces sclerosis, resolves osteolytic foci and, in company with bone formation in the fibrous mantle, restores the subchondral plate. 3. Many important aspects of the pathogenesis of osteoarthritis and of its partial repair by osteotomy remain to be elucidated


The Journal of Bone & Joint Surgery British Volume
Vol. 50-B, Issue 1 | Pages 116 - 127
1 Feb 1968
Clough JR Price CHG

1. The clinical, radiological, operative and histological features of twelve aneurysmal bone cysts are recorded. 2. Attention is drawn to atypical features, and the problem of diagnosis is discussed. 3. It is recommended that treatment should be complete excision, except where this would interfere with function. 4. Various theories on pathogenesis are considered and favour given to the view that these cysts result from a local change in haemodynamics occurring possibly in a pre-existing lesion


The Journal of Bone & Joint Surgery British Volume
Vol. 80-B, Issue 5 | Pages 907 - 908
1 Sep 1998
Hutchinson JW Tierney GM Parsons SL Davis TRC

In a series of 12 patients with inoperable gastric carcinoma who had treatment with a synthetic matrix metalloproteinase inhibitor (Marimastat) for more than one month, six developed a frozen shoulder or a condition resembling Dupuytren’s disease. This suggests that the matrix metalloproteinases, a family of naturally occurring proteinases, may be involved in the pathogenesis of these two conditions. Our observation opens avenues for further research which could lead to local or systemic therapeutic interventions for frozen shoulder and Dupuytren’s disease


The Journal of Bone & Joint Surgery British Volume
Vol. 71-B, Issue 2 | Pages 205 - 208
1 Mar 1989
Humphreys S Spencer J Tighe Cumming R

The occurrence of osteonecrosis following renal transplantation is well recognised but its pathogenesis remains unknown. We have quantified the number of empty osteocytic lacunae in the subchondral bone of femoral heads from a control group of patients, and compared these with femoral heads from a group of renal transplant recipients without evidence of overt osteonecrosis. There is a significant increase in empty osteocytic lacunae in renal transplant patients. We conclude that loss of osteocytes precedes other manifestations of osteonecrosis


The Journal of Bone & Joint Surgery British Volume
Vol. 44-B, Issue 4 | Pages 790 - 793
1 Nov 1962
Teare RD Bowen DA Drury RA

1. Three cases of acute peptic ulceration are reported after cerebral fat embolism complicating skeletal injuries. In two instances death occurred after perforation of an ulcer, and in the third intestinal haemorrhage led to death. 2. Although intracranial lesions and peptic ulceration have been reported on many occasions, so far as we know cerebral fat embolism as a cause has not been previously recognised. 3. The possible pathogenesis is discussed


The Journal of Bone & Joint Surgery British Volume
Vol. 81-B, Issue 3 | Pages 552 - 554
1 May 1999
Crawford R Puddle B Hunt N Athanasou NA

We reviewed histologically the incidence and pathogenesis of the deposition of calcium pyrophosphate dihydrate (CPPD) crystals in the pseudocapsule, femoral and acetabular membranes and periprosthetic tissue at revision of 789 cases of failed total hip replacement. In 13, periprosthetic tissues were found to have deposits of CPPD crystals in areas of cartilaginous metaplasia; four also showed evidence of localised deposition of amyloid. None of the patients had a history of chondrocalcinosis in the hip or other joints. Cartilaginous metaplasia and other changes in periprosthetic tissues may predispose to the deposition of CPPD and associated localised amyloid


The Journal of Bone & Joint Surgery British Volume
Vol. 67-B, Issue 5 | Pages 780 - 784
1 Nov 1985
Bell S Campbell P Cole W Menelaus M

We present three cases of a previously undescribed condition characterised by unilateral tibia vara associated with an area of focal fibrocartilaginous dysplasia in the medial aspect of the proximal tibia. The three children affected were aged 9, 15 and 27 months respectively. Two required tibial osteotomy, but in one the deformity resolved without treatment. The pathogenesis of the focal lesion remains conjectural; the most likely explanation is that the mesenchymal anlage of the tibial metaphysis has, for unknown reasons, developed abnormally at the insertion of the pes anserinus


The Journal of Bone & Joint Surgery British Volume
Vol. 64-B, Issue 3 | Pages 269 - 275
1 Jun 1982
Catterall A Pringle J Byers P Fulford G Kemp H Dolman C Bell H McKibbin B Ralis Z Jensen O Lauritzen J Ponseti I Ogden J

There are differences of opinion about the pathogenesis of Perthes' disease. All are agreed that it is due to ischaemia, but the cause of this and the size and number of infarctions are in dispute. Through the generosity of the contributors six whole femoral heads and core biopsies of five other cases have been studied radiographically and histologically. The findings ranged from an ischaemic arrest of ossification in the capital articular cartilage without infarction to multiple complete infarctions of the epiphysial bone. The ensuing reparative process contributes to the pathology, which is of a range to warrant grading or grouping


The Journal of Bone & Joint Surgery British Volume
Vol. 63-B, Issue 4 | Pages 610 - 613
1 Nov 1981
Mizrahi J Solomon L Kaufman B Duggan T

A method for direct measurement of the local pressures in the acetabular cartilage is described. Pressure transducers were introduced into the subchondral bone and positioned there in contrast with the cartilage: the transducers were calibrated in situ. Twelve cadaveric hips were prepared in this way and the pressures were measured with the joint loaded in flexion, extension, abduction, adduction, and in lateral and medial rotation. The highest pressures were recorded in the anterior and posterior segments of the acetabulum; the lowest pressures were constantly found at the zenith of the joint. The relationship of these findings to the pathogenesis of osteoarthritis is considered


The Journal of Bone & Joint Surgery British Volume
Vol. 62-B, Issue 3 | Pages 300 - 306
1 Aug 1980
Sutherland A Savage J Paterson D Foster B

The nuclide bone-scan will reliably diagnose Perthes' disease with a sensitivity of 0.98 and a specificity of 0.95. The comparable figures for radiographic sensitivity and specificity are respectively 0.92 and 0.78. In addition, it is possible on the scan to recognise the onset of revascularisation of the femoral capital epiphysis some months before there are radiographic signs of new bone formation. Scintigraphy also suggests that in some cases of transient synovitis there may bae a period of reversible ischaemia of the capital epiphysis, which may have relevance to the pathogenesis of Perthes' disease


The Journal of Bone & Joint Surgery British Volume
Vol. 61-B, Issue 2 | Pages 169 - 171
1 May 1979
Mariani P Caruso I

An electromyographic investigation of patients with subluxation of the patella has been carried out on the parts of the extensor apparatus which actively contribute to the alignment of the patella, both before and after the operation to correct this disorder. The electromyographic pictures have revealed a sharp fall in the activity of the vastus medialis, with full recovery to normal values after a corrective operation. Even if the aligning function of the patella is altered by a variety of factors, the present study confirms the importance of the vastus medialis in the pathogenesis of malalignment of the extensor mechanism


The Journal of Bone & Joint Surgery British Volume
Vol. 56-B, Issue 1 | Pages 121 - 129
1 Feb 1974
Magyar É Talerman A Fehér M Wouters HW

1. Clinical, radiological and pathological findings in seven cases of rheumatoid arthritis with giant bone cysts are presented. 2. In three cases the large cysts represented massive involvement of subchondral bone by rheumatoid granulation tissue; in two cases the cysts were due to rheumatoid nodules, and in two other cases the diagnosis was made only on the radiological findings. 3. The pathogenesis of this condition is discussed. It is suggested that cystic bone lesions in rheumatoid arthritis can arise either by replacement of subchondral bone by the rheumatoid process, or by the formation of rheumatoid nodules within the bone


The Journal of Bone & Joint Surgery British Volume
Vol. 45-B, Issue 4 | Pages 709 - 718
1 Nov 1963
Ling RSM

1. The families of fifty patients with Dupuytren's disease have been investigated for its presence. 2. Familial occurrence has been found to be considerably higher than has been reported hitherto. 3. The findings suggest that genetic factors are of extreme importance in the pathogenesis of the common form of Dupuytren's disease. 4. A single gene, behaving as a Mendelian dominant, is likely to be involved. 5. Dupuytren's disease may not be a homogeneous condition from the pathogenic standpoint


Bone & Joint Research
Vol. 9, Issue 9 | Pages 578 - 586
1 Sep 2020
Ma M Liang X Wang X Zhang L Cheng S Guo X Zhang F Wen Y

Aims

Kashin-Beck disease (KBD) is a kind of chronic osteochondropathy, thought to be caused by environmental risk factors such as T-2 toxin. However, the exact aetiology of KBD remains unclear. In this study, we explored the functional relevance and biological mechanism of cartilage oligosaccharide matrix protein (COMP) in the articular cartilage damage of KBD.

Methods

The articular cartilage specimens were collected from five KBD patients and five control subjects for cell culture. The messenger RNA (mRNA) and protein expression levels were detected by quantitative reverse transcription PCR (qRT-PCR) and western blot. The survival rate of C28/I2 chondrocyte cell line was detected by MTT assay after T-2 toxin intervention. The cell viability and mRNA expression levels of apoptosis related genes between COMP-overexpression groups and control groups were examined after cell transfection.


The Journal of Bone & Joint Surgery British Volume
Vol. 74-B, Issue 2 | Pages 219 - 223
1 Mar 1992
Mahale Y Silver

We report 13 patients with missed bilateral facet dislocation of the lower cervical spine who subsequently developed severe spinal-cord involvement. There were more women and the patients were older than in most groups with spinal injury. The commonest cause was a fall, and paralysis appeared from six to 48 hours after injury in most patients. Ten patients made some recovery after late reduction but three remained totally paralysed. We discuss the pathogenesis of the late cord lesion and the reasons for delay in diagnosis


The Journal of Bone & Joint Surgery British Volume
Vol. 72-B, Issue 3 | Pages 475 - 479
1 May 1990
Sanguinetti C Greco F De Palma L Specchia N Falciglia F

We obtained specimens of growth-plate cartilage from four patients with osteogenesis imperfecta. Light microscopy showed structural changes in the tissue and morphological changes in chondrocytes and matrix, particularly in the hypertrophic zone. There were changes in the process of calcification in the primary mineralisation zone of the cartilage. We also found histochemical changes in the matrix glycosaminoglycans (GAGs) in the zones where physiological mineralisation was disturbed and where the trabeculae were interrupted and poorly mineralised. In addition to the known molecular defects in collagen, changes in GAGs and non-collagenous proteins are important factors in the pathogenesis of the disease


The Journal of Bone & Joint Surgery British Volume
Vol. 53-B, Issue 1 | Pages 30 - 36
1 Feb 1971
Macdonald D

1. The literature of primary or idiopathic protrusio acetabuli is reviewed with particular reference to familial and racial influence on pathogenesis. 2. The radiological criteria of a "deep" acetabulum and of a "protruded" acetabulum are discussed. 3. Four generations of a family are presented in which all three members of the second generation showed marked protrusio acetabuli. In the remaining generations most members appeared to have abnormally deep acetabuli. 4. It is concluded that this family shows a strong familial tendency to deep or intruded acetabuli. The family tree, though incomplete, suggests a genetic influence ofa dominant type


The Journal of Bone & Joint Surgery British Volume
Vol. 31-B, Issue 3 | Pages 426 - 432
1 Aug 1949
Simmonds FA

1. The "frozen" shoulder syndrome is due to an inflammatory lesion in the musculotendinous cuff invoked by a local area of degeneration. 2. The available evidence suggests that the primary site of the degenerative lesion is in the supraspinatus tendon. 3. Other causes of shoulder pain which must be differentiated from "frozen" shoulder are peritendinitis of the long head of biceps, degeneration or tears of the supraspinatus, and calcified deposits in the supraspinatus. 4. An explanation of the pathogenesis of lesions of the musculo-tendinous cuff is submitted in which the different types of clinico-pathological syndrome are correlated. This hypothesis is in accord with the experimental, clinical and operative findings


The Journal of Bone & Joint Surgery British Volume
Vol. 74-B, Issue 6 | Pages 923 - 927
1 Nov 1992
Sanderson P Morris M Stanley J Fahmy N

We studied prospectively the relationship between serum lipids and Dupuytren's disease of the hand in 85 patients, 65 men and 20 women. The Dupuytren patients had significantly higher fasting serum cholesterol and triglyceride levels than did the controls (p < 0.001). The raised levels of serum lipids appeared to be associated with the pathogenesis of Dupuytren's disease, and this may help to explain the high incidence of Dupuytren's disease in alcoholic, diabetic and epileptic patients, since these conditions are also associated with raised serum lipid levels


The Journal of Bone & Joint Surgery British Volume
Vol. 44-B, Issue 2 | Pages 302 - 318
1 May 1962
Stewart MJ Gilmer WS Edmonson AS

1 . Twenty patients with fibrous dysplasia, confirmed histologically, are reported and discussed in regard to classification, etiology, pathogenesis and treatment. The various fibrous or fibrocystic lesions of bone are characterised briefly for purpose of contrast, and the position of fibrous dysplasia in this heterogeneous collection is suggested. 2. The classification of fibrous dysplasia based on the degree of skeletal involvement is used, and the diagnostic, therapeutic and prognostic implications of this classification emphasised. The authors endorse the opinion that fibrous dysplasia is a developmental defect. Clinical, histological and radiographic evidence is presented to point to the distinct evolution of the monostotic lesions, to which a positive and aggressive approach is recommended