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47 Cards in this Set
- Front
- Back
Bubbly or lytic lesions |
FEGNOMASHIC - Fibrous Dysplasia, Enchondroma, Eosinophilic Granuloma, Giant Cell Tumor, Non-ossifying fibroma, osteoblastoma, Metastitc disease, Myeloma, Aneurysmal Bone Cyst, Solitary (unicamaral bone cyst), HPT, Infection, Chondroblastoma
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fibrous dysplasia
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no periosteal reaction, mention adamantinoma if in tibia or jaw; pelvis, proximal femur, ribs, skull, long lesion in long bone, expansile medullary lytic lesion, ground glass, well-defined sclerotic margin, bowing deformities, base of skull sclerotic, hot on bone scan, cherubism in mandible and maxilla, craniofacial in facial and frontal bones, pseudoarthrosis of tibia, Mccune Albright is polyostotic FD with café-au-lait spots with precocious puberty
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enchondroma
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must have calcifications except in phalanges, no periostitis; tubular bones, chondroid calcifications, endosteal scalloping, pain is malignant, Ollier’s enchondromatosis, Mafucci’s enchondromatosis with multiple ST hemangiomas
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EG
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age<30; lytic lesion can look aggressive, skull lesion beveled-edge appearance, sequestrum, floating tooth, vertebra plana, lung dz, pituitary, RES
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GCT
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epiphyses must be closed, must be epiphyseal and abut the articular surface in long bones, eccentric, well-defined but nonsclerotic border except in flat bones; long tubular bone > spine or sacrum, 50% at knee
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NOF
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age<30, no periostitis, cortically based; metaphysis
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osteoblastoma
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mention with ABC even if age>30, especially in posterior elements of spine
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mets
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age>40; renal and thyroid
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myeloma
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age>40; plasmacytoma in ilium and sacrum, cold on bone scan; vertebral bodies destroyed before pedicles, axial skeleton, long bones, punched-out lytic lesions, generalized osteopenia, skeletal survey more sensitive
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ABC
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age<30, expansile, eccentric, pain, fluid-fluid levels on MR; posterior elements of spine, metaphysis of long bones, pelvis
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SBC (Unicamaral Bone Cyst)
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age<30, central, no periostitis; proximal humerus, proximal femur, calcaneus, fallen fragment sign
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Hyperparathyroidism
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brown tumor, must have other evidence of HPT
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infection
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always mention
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chondroblastoma
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age<30, epiphyseal
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chondromyxoid fibroma |
mention with NOF, no calcified matrix
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Mention in every case of bubbly or lytic lesions |
Age<30 – infection, EG; age>40 – infection, mets, myeloma |
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Multiple Lytic Lesions |
FEEMHI: fibrous dysplasia, enchondromas, EG, mets, myeloma, HPT, infection
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Benign Appearing Rib Lesions |
fibrous dysplasia, ABC, mets, myeloma, enchondroma, EG
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Lytic epiphyseal lesion (also apophyseal, carpal and tarsal bones, patella)
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chondroblastoma, infection, EG, GCT, geode; age>40 – add mets and myeloma and remove chondroblastoma
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Lytic lesion in posterior elements of spine
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OAT: osteoblastoma, ABC, TB
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Exclude these lytic lesions if age>30
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CANES: chondroblastoma, ABC, NOF, EG, SBC
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Lesions that have no pain or periostitis
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FENS: fibrous dysplasia, enchondroma, NOF, SBC
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Bony sequestrum
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FILE: fibrosarcoma, infection, lymphoma, EG, osteoid osteoma (mimic)
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Geodes |
CARD: CPPD, AVN, RA, DJD, trauma
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Sclerotic lesion age 20-40
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chondroblastoma, ABC, NOF, EG, SBC, fibrous dysplasia, infection, HPT (healing brown tumor), osteoid osteoma, giant bone island; age>40 – mets
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Endosteal scalloping
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ibrous dysplasia, enchondroma, cartilaginous tumor
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Wide zone of transition (permeative)
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mets + myeloma, reticulum cell sarcoma, Ewing’s sarcoma, infection, EG
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Malignant bone tumors: age<30
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Ewing Sarcoma, Osteosarcoma, Mets
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Ewing’s sarcoma
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diaphysis long bones > flat bones, aggressive, ST mass typical, medullary location
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osteosarcoma
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poorly defined intramedullary metaphyseal mass lesion extends through cortex, osteoid or chondroid matrix, aggressive periosteal reaction with Codman triangle or sunburst pattern
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osteosarcoma telangiectatic form
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purely lytic and simulates ABC, parosteal form is low-grade and seen in posterior distal femur with more mature ossification centrally
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mets in children
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neuroblastoma, leukemia/lymphoma, Wilm’s
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Malignant bone tumors: age>40
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mets + myeloma,chondrosarcoma
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chondrosarcoma |
pain, long bones, pelvis, ribs, clivus, most metaphyseal
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Malignant bone tumors: age 30-40
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GCT, Fibrosarcoma, Malignant Fibrous Histiocytoma, Reticulum Cell Sarcoma
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GCT
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if lung mets or recurrance
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parosteal osteosarcoma
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densest calcification is central
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fibrosarcoma
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almost always lytic
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malignant fibrous histiocytoma
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mention with fibrosarcoma, aggressive, large soft tissue mass
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reticulum cell sarcoma
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primary lymphoma of bone, looks like Ewing’s sarcoma, often asx
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Permeative lesion in child
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Ewing’s sarcoma, infection, EG
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Permeative lesion in older pt
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infection, mets, myeloma, malignant fibrous histiocytoma, reticulum cell sarcoma
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Soft tissue tumors
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MFH, liposarcoma (may or may not have fat), synovial sarcoma (usu extraarticular), synovial osteochondromatosis (multiple Ca++ loose bodies, jt effusion, erosions, destruction; knee, hip, elbow; mimics PVNS if not Ca++), pigmented villonodular synovitis (hemosiderin deposits lining synovium, erosions, jt destruction, no joint space narrowing), hemangiomas (phleboliths, cortical holes, striated vertebral body)
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Malignant transformation of bony lesions
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fibrous dysplasia – fibrosarcoma, OSA, MFH; Paget’s – OSA; osteomyelitis with draining sinus – SCC; radiation – OSA, chondrosarcoma, MFH; bone infarct – fibrosarcoma, MFH; Ollier’s – chondrosarcoma; Maffucci’s – chondrosarcoma; osteochondroma – chondrosarcoma
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Cortical holes (pseudopermeative lesion)
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osteoporosis (metacarpal cortex less then ¼ to 1/3 of metacarpal), radiation, hemangiomas
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Focal cortical thickening
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stress fracture, infection, osteoid osteoma
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Mets to bone |
PBKTL; P – mostly blastic, B – mixed, K – purely lytic, TL – mostly lytic |