Aims. After intercalary resection of a bone tumour from the
We investigated the clinical outcome of internal
fixation for pathological fracture of the femur after primary excision of
a soft-tissue sarcoma that had been treated with adjuvant radiotherapy. A review of our database identified 22 radiation-induced fractures
of the
We retrospectively reviewed 101 consecutive patients
with 114 femoral tumours treated by massive bone allograft at our
institution between 1986 and 2005. There were 49 females and 52
males with a mean age of 20 years (4 to 74). At a median follow-up
of 9.3 years (2 to 19.8), 36 reconstructions (31.5%) had failed.
The allograft itself failed in 27 reconstructions (24%). Mechanical complications such as delayed union, fracture and
failure of fixation were studied. The most adverse factor on the
outcome was the use of intramedullary nails, followed by post-operative
chemotherapy, resection length >
17 cm and age >
18 years at the
time of intervention. The simultaneous use of a vascularised fibular
graft to protect the allograft from mechanical complications improved
the outcome, but the use of intramedullary cementing was not as
successful. In order to improve the strength of the reconstruction and to
advance the biology of host–graft integration, we suggest avoiding
the use of intramedullary nails and titanium plates, but instead
using stainless steel plates, as these gave better results. The
use of a supplementary vascularised fibular graft should be strongly
considered in adult patients with resection >
17 cm and in those
who require post-operative chemotherapy.
Aims. Osteoarticular reconstruction of the distal
Aims. The epiphyseal approach to a chondroblastoma of the intercondylar notch of a child’s distal
Aims. Giant cell tumours (GCTs) of the proximal
Aims. Accurate estimations of the risk of fracture due to metastatic bone disease in the
Aims. The consensus is that bipolar hemiarthroplasty (BHA) in allograft-prosthesis composite (APC) reconstruction of the proximal
Deformity of the proximal
The purpose of this study was to assess whether
the use of a joint-sparing technique such as curettage and grafting was
successful in eradicating giant cell tumours of the proximal
Excision of the proximal
Monostotic fibrous dysplasia of the proximal
femur has a variable clinical course, despite its reported limited tendency
to progress. We investigated the natural history and predisposing factors
for progression of dysplasia in a group of 76 patients with a mean
follow-up of 8.5 years (2.0 to 15.2). Of these, 31 (41%) presented
with an asymptomatic incidental lesion while 45 (59%) presented
with pain or a pathological fracture. A group of 23 patients (30%)
underwent early operative treatment for pain (19: 25%) or pathological
fracture (4: 5%). Of the 53 patients who were initially treated non-operatively,
45 (85%) remained asymptomatic but eight (15%) needed surgery because
of pain or fracture. The progression-free survival of the observation
group was 81% (. sd. 6.4%) at five-years follow-up. An initial
presentation of pain (p <
0.001), a limp (p <
0.001), radiological
evidence of microfracture (p = 0.001) and younger age (<
17 years)
(p = 0.016) were significant predisposing factors for disease progression. The risk of experiencing pain or pathological fracture is considerable
in monostotic fibrous dysplasia of the proximal
We report positive and negative factors associated with the most commonly-used methods of reconstruction after pathological fracture of the proximal
Endoprosthetic reconstruction following resection of 31 tumours of the proximal
We describe 25 patients who were treated for a tumour of the proximal
We report our experience of treating 17 patients with benign lesions of the proximal
We investigated whether improvements in design have altered the outcome for patients undergoing endoprosthetic replacement of the distal
The aim of this study was to assess a specific
protocol for the treatment of patients with a parosteal osteosarcoma of
the distal
Failure of massive knee endoprostheses implanted for malignant tumours of the distal
We report our results in 24 children with malignant primary bone tumours of the distal