The purpose of this paper is to document two unusual cases of Ewing's sarcoma of the hand. The clinical picture was one that did not include fever, leukocytosis, increased sedimentation rate, or cortical sclerosis. The roentgen appearance was
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distinctly different from that of classic Ewing's tumor in the larger long bones. Both patients were treated by adequate resection of the tumor and are tumor-free two and three years, respectively, after surgery.