Tumours Name some characteristics of benign bone tumours? Relatively common
Usually recognised by their position and radiographic
appearance
Require careful assessment to exclude malignancy
Majority occur in the adolescent / young adult
Tumours cease growth when skeletal maturity reached
What is an Osteoid Osteoma? M > F, presents between age 10 – 25 yrs Severe and persistent pain – typically relieved by aspirin Femur, tibia – most commonly. Spine - usually pedicle Lesion in cortex of bone with reactive sclerosis around a radiolucent central nidus Nidus – immature osteoid tissue + highly vascular cellular tissue Rarely larger than 1 cm in diameter If doubt CT / MRI scan – useful Bone scan – intense “hot spot” in affected area Treatment surgical excision, if complete, is curative What is a Chondroma? Most common of all bone tumours Two varieties – enchondroma and ecchondroma Enchondroma – confined within intact cortex
causes cortex to become
structurally thin Ecchondroma – protrudes beyond cortex of bone
Both most common in tubular bones of hands and feet
Less common in larger tubular / flat bones Malignant transformation Rare in solitary chondromas
25% of cases in multiple enchondromatosis (Ollier’s
disease) Treatment excision and currettage ± bone grafting What is an Osteochondroma? Comparatively common tumour Typically occurs on the external surface of metaphysis Distal femur, proximal tibia, proxiaml humerus ? Result of failure of bone remodelling during growth Typical pedunculated / sessile growth arising from metaphysis Usually identified incidentally after minor injury Always stop growing at skeletal maturity Any enlargement thereafter – treat with suspicion Treatment Excision if causing symptoms or pain / enlargement in adult What is a Solitary Bone Cyst? Predominantly in adolescent boys Most common sites proximal humerus / femur Often presents as pathological fracture Radiographic appearance Ovoid radiolucent area with thinning of the overlying cortex Tends to abut growth plate, never penetrates it Treatment If tumour found in association with fracture – may resolve spontaneously as union proceeds (usually at normal rate) If this does not occur – excision and curettage ± bone grafting Some evidence that intracystic injection with methylprednisolone as effective as surgery What is an Aneurysmal Bone Cyst? Characterised by blood-filled cavities separated by fibrous septa and areas of new bone formation Affects adolescents / young adults Metaphyseal regions of long bones / vertebral column Radiographic appearance Eccentric radiolucent lesion expanding beyond margins of the thinned cortex Growth may be extremely rapid – often mistaken as malignant Treatment Complete surgical excision usually curative ? Radiotherapy alone / in combination with surgery What are Juxta-Articular Bone Cysts? Also known as interosseous ganglions Mature adults – incidence ↑ with age Common in distal tibia, acetabulum and carpus Radiographic appearance Well defined, radiolucent cystic space with sclerotic margin Similar to the cysts of OA ? Cause - ? Fibrous metaplasia with superimposed ucoid degeneration Treatment Deroofing and currettage ± bone graft (if large) What are Fibrous Cortical Defects? Occurs in metaphysis during growth If incorporated within bone – non-ossifying fibroma Most are incidental x-ray anomalies or present as fractures Well circumscribed lesions – difficult to differentiate from simple cysts Treatment No specific treatment necessary unless it is a cause of recurrent fracture – curettage and bone grafting usually curative What is a Haemangioma? A few occur in skull / long bones Can present as pathological fracture of long bones Majority affect vertebral body – usually incidental finding Radiographic appearance Increased density and striations in vertebral body Absence of bone destruction / expansion Can be mistaken for malignancy MRI useful to establish diagnosis Treatment Symptomless – conservative mx Pathological fracture long bone – stabilization ± fixation Radiotherapy to inaccessible areas for Haemangioma in spine symptomatic lesions only What is a Eosinophilic Granuloma? Histiocytosis “X” One of a family of conditions which includes Hand-Schuller-Christian and Letterer-Swie disease Presents in adolescence Skull, mandible, vertebral bodies, ribs, metapysis long bones Pain is presenting feature Radiographic appearance Lucent area with cortical thinning Vertebral body lesions have a typical flattened, dense appearance Treatment Biopsy is essential – currettage usually erradicates it Multiple lesions – suggests more complex form of disease