We present a case of subperiosteal giant-cell reparative granuloma followed over six years showing the complete evolution from the early phase of subperiosteal haematoma to the end stage of an ossified haematoma. Such lesions, although they are histologically similar to true giant-cell tumours, can be distinguished by the patients' age, their location on the diaphysis, and by their radiological and histological features

A benign chondroblastoma of bone is reported. It was unusual because it occurred in an old lady, in a toe, and it was not painful and radiologically resembled a chondroma. The coarsely lobulated tumour showed a varied microscopic appearance, but it consisted chiefly of closely packed sheets of small, round polygonal or fusiform cells. There was some calcification present. The literature is reviewed

Two cases of adamantinoma of the tibia are reported. The first patient has survived twenty years after above-knee amputation and shows no sign of recurrence. The second patient shows no evidence of recurrence two and a half years after amputation through the knee. The clinical picture of the tumour is described and the theories of histogenesis are outlined

1. A case of primary intraosseous liposarcoma is described which was producing tumour bone (osteo-liposarcoma: malignant mesenchymoma) in the right fibula of a boy of fifteen. 2. Death occurred from pulmonary metastases nine months after excision and cobalt teletherapy. 3. Only one similar case has been reported

Two cases of benign osteoblastic tumours of the spine, occurring in young patients, and presenting as expanding osteolytic lesions with some central calcification and ossification, are described. It is suggested that they represent a condition allied to, but usefully separated from, osteoid osteoma of bone. The name osteogenic fibroma of bone, proposed by Lichtenstein for this type of case, is accepted

In this retrospective study, we analysed the clinical features of neurilemoma when it is located in muscle. Twelve patients had an intramuscular neurilemoma as shown on magnetic resonance (MR) scans and confirmed at operation. In six it was located in the upper limb, in five in the lower limb, and in one in the back. The mean age of the patients was 41 years (12 to 58). Nine complained only of a palpable mass and the other three of a mass with slight tenderness. None had neurological symptoms or signs, such as radicular pain, a positive Tinel sign, or motor weakness. There were no postoperative complications or recurrence of the tumour after a mean follow-up of two years (1 to 10)

Seven patients with Ewing's sarcoma of the pelvis were treated by chemotherapy followed by wide resection of the primary tumour. Although good function after operation is possible, survival in this series reflects the poor prognosis associated with the disease; two patients died, two are alive with local recurrence and metastases and three patients are alive with no evidence of disease

1. A case of massive osteolysis of the bones and soft tissues of the left foot is reported. 2. Arteriography revealed slowed circulation in the foot, hut the tumour vessels did not fill with contrast medium. 3. Two years after below-knee amputation of the left leg and four years after the onset of symptoms, the patient appeared to be free from disease

1 . A case of parosteal osteoma with histologically low-grade sarcomatous areas is described. 2. Arteriography revealed abnormal arteries, the histological appearances of which are described. 3. Vascular shunts indicative of low-grade malignancy were also seen. 4. Reasons are given for accepting the view that this lesion is a tumour, originally benign, but liable to the development of low-grade malignancy

1. A case is described in which a malignant tumour developed in the soft tissues at the site of a bone-plating operation performed thirty years before. 2. The plate and screws were found to be composed of dissimilar metals and a difference of potential existed between them. 3. A careful consideration of the history and clinical course indicates that the tumour arose because of the presence of the metals

We report a patient with a subperiosteal ganglion cyst of the tibia which was imaged by radiography, arthrography, CT and MRI. The images were correlated with the arthroscopic surgical and histological findings. Spiculated formation of periosteal new bone on plain radiographs led to the initial suspicion of a malignant tumour. Demonstration of the cystic nature of the tumour using cross-sectional imaging was important for the precise diagnosis. Communication between the ganglion cyst and the knee was shown by a delayed arthrographic technique, and the presence of this communication was confirmed at arthroscopy and surgically

Two cases of skeletal amyloidosis are described. In one the disease existed for many years, progressively destroying several vertebral bodies. There was no evidence of chronic infection, myelomatosis or cancer. In the other case myelomatosis was the primary disease but the first manifestation was a cystic tumour of the humerus. Not until several years later did typical bone lesions and Bence-Jones protein reveal the true nature of the disease

1. Six patients suffering from spontaneous posterior interosseous paralysis are described. 2. Two were due to benign tumour and four due to traumatic neuritis, three of which were associated with minor hyperextension injuries to the elbow joint and one with long standing cubitus varus. 3. Surgical exploration was performed in each patient with recovery of nerve function

1. Twenty-five cases of benign giant-cell tumour of bone, treated at Westminster Hospital, London, are reported. 2. The diagnosis can often be made on clinical and radiographic grounds alone but biopsy is sometimes necessary and seldom, if ever, contra-indicated. 3. Some cases may best be treated by excision, but in general irradiation is the treatment of choice. 4. Details of treatment by irradiation are given

Chondrosarcomas arising from soft tissues are rare. Two different varieties are described, myxoid and mesenchymal. We have collected nine cases of the tumour, five myxoid and four mesenchymal, from a review of 513 cases of chondrosarcoma seen between 1904 and 1988. We report the principal clinical, radiographical and histological differences between the two varieties and discuss their surgical treatment and prognosis

An operation is described in which a microvascular technique was used to transfer a living fibula, with its vascular pedicle intact, to replace the lower end of the radius after massive resection for giant-cell tumour. Angiography carried out six weeks later showed that the grafted bone was viable. Six months after operation the transplanted fibula showed no osteoporosis or bone resorption and bony union at the junction of host and graft

1. A series of thirty-two cases of chondromyxoid fibroma is reported. 2. The clinical, radiographic and pathological features are described. 3. The rarity of the tumour and of malignant change is stressed. 4. Excision or block resection is preferred to curettage as a method of treatment, because of the liability to recurrence after curettage. 5. It is suggested that the designation "fibromyxoid chondroma" is more appropriate than the usual designation "chondromyxoid fibroma"

1. A clinical, radiological and pathological study of sixty-nine cases of epiphysial chondroblastoma has been made. 2. The nature of the tumour is discussed and its clinical and radiographic features are described. A special type is described, for which the name "cystic chondroblastoma" is suggested. 3. The results of treatment are described and the generally benign behaviourof the lesion is noted. 4. The occurrence of malignant change is noted and discussed

1. Two cases are reported in which there was diffuse fibro-fatty overgrowth or tumour formation involving the adipose tissue of the median nerve. In each the diagnosis was confirmed by operation and histological examination. 2. The first case is an example of the developmental abnormality usually referred to as "macrodystrophia lipomatosa." The second case should be termed fibrolipoma. 3. The literature is reviewed; no case of fibrolipoma has been recorded

1. Nine cases of haemangiopericytoma are described and the treatment is discussed. 2. Six of the patients had a recurrence of the tumour after local excision. 3. Four patients developed metastases and died. All had been treated by surgery and cobalt 60 beam radiation. 4. Five of the patients show no further disease. Of these, two received cobalt 60 beam radiation after surgical treatment