BONE TUMOURS
introductionIn general bone tumours can be classified into : A- primary . B- secondary . Primary bone tumours classification : Most classification of bone tum.are based on the recognition of the dominant tissue in the various lesion ; e.g. bone forming tum. Or cartilage forming tum. Etc.
Cell type benign malignant Bone osteoid osteoma osteosarcoma Cartilage chondroma chondrosarcoma Fibrous t. Fibroma fibrosarcoma b. Marrow eosinophilic Ewing sarcoma, granuloma myeloma Vascular haemangioma angiosarcoma Uncertain giant cell tumor malignant giant cell tumor Tumor-like lesions: bone cysts , fibrous dysplasia , brown tumor
Surgical staging
Sarcoma are divided into :Stage 1 :all low grade sarcoma .Stage 2 :all high grade sarcoma .Stage 3 : all metastatic tumors .Enneking”s classification :Type A : all the intracompartmental tumors .Type B : all the extracompartmental tumors .Radiological investigation
A- plain x- ray. 1- site of the lesion . 2- size of the lesion . 3- shape of the lesion . 4- density of the lesion . 5- homogenous or non homogenous lesion . 6- boundary of the tumor and the transitional zone . 7- presence or absence of periosteal reaction .Signs of aggressive lesions in x-ray
1- rapidly enlarged tumor . 2- wide transitional zone . 3- destruction of the cortex . 4- periosteal reaction .B- bone scan e.g Tc99. C- C.T scan. D- MRI
Principles of treatment
1- benign asymptomatic lesion need no treatment ; if the diagnosis is not 100% sure then biopsy is indicated . 2- benign symptomatic :painful or continue grow after arresting of growth : it require biopsy and marginal excision . 3- suspected malignant :it need detailed investigation for knowing the type and the staging to decide the way of treatment .Benign bone tumor
Osteochondroma(bone exostosis)This is one of the commonest benign bone tumor ; it is developmental tumor start as small over growth of cartilage at the edge of the physeal plate , and grow to boney protuberance covered by cap of cartilage. The commonest sites are the fast growing ends of the long bones , and it continue to grow until the bone stop growing at the end of the growth period . Any further increase in size after this period is mean malignant changes .
The patient is usually teenager or young adult presented with a lump near the end of the long bones , some time there is pain .Multiple lesions can be present as part of heritable disorder (multiple exostosis) called diaphyseal acalasis.X-ray : boney projection from the metaphysis of the long bone, large lesion may have cauliflower – like lesion .Treatment : excision .
Osteoid osteoma
Small tumor of bone cause symptoms out of all proportion to its size . Patient usually under 30 years old , male more than female , it can affect all bones except the skull and mainly the femur and tibia . The patient complain from persistent pain which typically revealed by salicylate .X-ray :plain x-ray show small radiolucent area (nidus) in the diaphysis surrounded by area of sclerosis and cortical thickening . Tc99 : show localized increased activity . Treatment : by complete excision of the nidus