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The final diagnosis is parachordoma.
Parachordoma:
-- rare soft-tissue tumor resembling extraskeletal myxoid chondrosarcoma and chordoma
-- age from 7 to 62 years (mean, 35 years)
-- Sites: subfascial masses of the thigh, arm, chest wall, and buttocks
-- Histopath: large, rounded eosinophilic cells embedded in a matrix that varied from myxoid to densely hyaline and multivacuolated (physaliferouslike)
cells
-- Special stains: matrix stained with Alcian blue (ph2.0)
-- IHC:
* strongly expressed CK 8/18, but not the others
* also positive for: expressed EMA, S-100, and vimentin
-- D/Dx:
* chordoma --> Positive for CK 8/18 (15 of 15) and CK 1/10
* extraskeletal myxoid chondrosarcoma --> consistently lacked CK