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Published byFarzad Ravari Modified over 7 years ago
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BONE TUMORs Dr.Farzad Ravari MPH, M.D Specialist Orthopedic Surgeon
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SIGN & SX *MOST COMMON AGE< 30 Y/O IN PRIMARY TUMOR *>50 Y/O IN METASTATIC TUMORS *PAIN ESP.AT NIGHT OR REST *MASS *PATHOLOGIC FX
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P/E LOCATION SHAPE CONSISTENCY MOBILITY TENDERNESS SKIN TEMPERATURE LYMPH NODE
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CLASSIFICATION BENIGN STG 1= LATENT: intra capsular,no sx,xr= thinscelerotic border >>>>> NO NEED TO TREAT STG 2= ACTIVE: INTERACAPSULAR+RAPID GROWING+PATH FX >>>>> TREAT= CURTAGE STG 3= EXTRACAPSULAR+ PATH FX,MRI=MASS TREAT= WIDE OR RADICAL RESECTION
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MALIGNANT TUMOR STG 1A= LOW GRADE+INTERA COMPARTMENTAL STG 1B= LOW GRADE +EXTERA COMP. STG 2 A=HIGH GRADE +INTERACOMPARTMENTAL STG 2 B = HIGH GRADE + EXTRA COMP. STG 3= + METASTASIS
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ENNEKING 4 QUESTIONS 1-ANATOMIC LOCATION 2- TUMOR ACTION TO BONE(DESTRUCTION PATTERN) BONE REACTION TO TUMOR(PERIOSTEAL REACTION) INTERATUMORAL DENSITY
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ANATOMIC LOCATION SPINE POST ELEMENT=ABC ANT ELEMENT CHILD=HT-X,HEMANGIOMA ADULT=CHORDOMA, HEMANGIOMA, PAGET, MM,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,,
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EPIPHYSIS - METAPHYSIS CHONDROBLASTOMA L.G. OSTEO. SARCOMA EOS. GRANULOMA DESMOID TUMOR AB C, UBC H.G OSTEO.SARCOMA OSTEOBLASTOMA FIBROUS DYSPLASIA GAINT CELL TUMOR
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DIAPHYSIS PARAOSTEAL FIB.DYSPLASIA HIST-X EWING SARCOMA OSTEOBLASTOMA ADAMANTINOMA LIPOMA METASTASIS MYOSITIS OSSIFICANT OSTEOSARCOMA CHONDROSARCOMA ECHONDROMA
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RIBS CHILD: FIBROUS DYSPLASIA EWING SARCOMA ADULT: EWING SARCOMA CHONDROSARCOMA FIBROUS DYSPLASIA MULTIPLE MYELOMA METASTASIS
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DESTRUCTIVE EFFECT GEOGRAPHIC PATTERN LESION >1 CM UBC FIB.DYSPLASIA CHONDRMYXOID FIBROMA NON OSS.FIBROMA GCT 50%
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MOTH EATEN PATTERN LESION 2-5 MM OSTEOMYELITIS GAUCHER METASTASIS CHONDROSARCOMA MYELOMA LYMPHOMA EOS.GRANULOMA
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PERMEATIVE LESION <1 MM OSTEOMYELITIS EWING SARCOMA OST.SARCOMA MYELOMA GAUCHER EOS.GRANULOMA
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PERIOSTEAL REACTION CODEMAN TRIANGLE ABC OSTEOMYELITIS GCT
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ONION SKIN EWING SARCMA OSTEOMYELITIS OSTEO SARCOMA
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SUNBURST OSTEOSARCOMA EWING SARCOMA PROSTAT METASTASIS MAJOR THALASEMIA SICKLE CELL ANEMIA
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DENSE THICK OSTEOID OSTEOMA TRAUMA INFECTION
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Reaction of Bone to Tumor REAM SCLEROSIS : BENIGN TUMOR BENDING: RICKETS, FIB.DYSPLASIA, PAGETS EXPANSION: 80% benign tumor, primary sarcoma,metastasis of kidney & thyroid Eccentric expansion: chon.mix.fibroma,abc, L.G SARCOMA FINGER IN BALLON SIGN :ABC
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INTERA TUMORAL DENSITY COLUMBOUS CLOUD OSTEOSARCOMA
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POP CORN ENCHONDROMA
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Spotty Density or Wind Blown CHONDROSARCOMA
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Ground Glass Appearance FIBROUS DYSPLASIA OSTEO SARCOMA
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Case presentation 65y/o male with kn p for 1mo P/E= Local tend in mjl Routin lab=WNL CXR=NAD Bone scan= Increase uptake in prox tibia
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MRI
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3 weeks later Biopsy done : Result no malignant cell detected Repeated biopsy =same
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6 MONTHS LATER Pain increase Knee instability Hip pain Limping Limb shortening Again biopsy= nothing
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7 months later Limping increase Shortening about 4cm Routin lab=WNL
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AFTER 8 MONTHS KNEE SLX HIP DESTRCTION WHEEL CHAIR BOUD
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??? ??? Z I G M A 4TH STAGE NEURO-PATHIC PHASE FTA ABS+++
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SYPHILIS 1 ST STG=10-90 days,>>>>>>>chancre 2 nd STG=4-10 wks after chancre>>skin rash, very contagious, mucosal sore 3 rd STG=nervous sx>>>> headache, stiff nk, paralysis 4 th STG=neuropathic &osteopathic >>>absorbsion of bones & destruction of joints
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