CHONDROSARCOMA
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Chondrosarcoma is a malignant tumor where the tumor cells produce cartilage matrix
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Age – in adults in 5th and 6th decade of life
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Site – Axial skeleton (more aggressive), medullary cavity of femur, humerus, ribs and rarely digits
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Imaging –
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They are located in metaphysis and extend into diaphysis producing radiolucent defect with scalloped inner cortex
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Thickening and inequality of the cortex are common radiographic finding
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Punctuate and stippled calcification are characteristic
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Gross –
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They are lobulated with grayish white or blue on cut section.
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Focal calcifications may be pressent
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Areas of mucoid degeneration or necrosis may occur.
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MIcroscopy
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Chondrosarcomas are graded into 3 groups
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Grade I – Low grade chondrosarcomas resembling enchondroma. Microscopic evidence of invasion into the adjacent bone and foci of entrapped entrapped bone within the tumor help in distinguishing it from enchondroma
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Grade II – Increased cellularity with increased nuclear size and distinct nucleoli. Focal myxoid change and binucleated cells can be seen
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Grade III – High grade chondrosarcoma characterized by marked cellular atypia, hypercellularity and high mitotic activity
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more than 10% of chondrosarcoma undergo dedifferentiation showing malignant spindle cells and bizarre giant cells
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Variants
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Mesenchymal chondrsarcoma
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Age– 2nd and 3rd decades of life
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Site – Any bone can be affected but has predilection for the maxilla, mandible and ribs
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1/3rd of lesions are present in soft tissue
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Imaging – osteolytic lesion with irregular calcification
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Morphology
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Gross – grayish white or yellow tumor mass
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Microscopy –
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Shows biphasic pattern
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majority is composed of small, uniform, round to spindle shaped cells with perivascular arrangement of cells that gives hemangiopericytoma like pattern
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In between the cells areas of cartllage or chondroid matrix is seen
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most common site of metastasis is lungs, but can metastasize to bones and soft tissue
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Clear cell chondrosarcoma
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least common variant of chondrosarcomas
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It is a low grade malignant tumor presenting in young adults, predominantly men
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Location – epiphysis of long bones commonly in the upper femur
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Imaging – well circumscribed mixed lucent and sclerotic defects often with a thin sclerotic border and scattered calcification
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Microscopy
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Tumor cells have abundant clear or pale eosinophilic, vacuolated cytoplasm rich in PAS positive glycogen which often lies between heavily calcified cartilage matrix and woven bone
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scattered giant cells are present
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IHC – strongly positive for S-100
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prognosis – they are indolent but locally aggressive.
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