JBJS | Ewing Sarcoma in an Octogenarian : A Case Report

The Journal of Bone & Joint Surgery, Volume 84, Issue 3

Case Reports | March 01, 2002

Ewing Sarcoma in an Octogenarian : A Case Report

Richard G. Levine, MD; Christopher M. Bono, MD; Meera Hameed, MD; Marcia Blacksin, MD; Anna C. Pavlick, MD; Charles Cathcart, MD; Joseph Benevenia, MD

The Journal of Bone & Joint Surgery. 2002; 84:445-448

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Extract

Ewing sarcoma is a round-cell bone tumor that most often affects older children and adolescents¹. Although less common, Ewing sarcoma in adults has been documented in clinical reports; the tumor primarily occurs in patients less than forty years of age, and the oldest patient in whom it was previously reported was sixty-one years of age¹. The prognosis in adults and their response to current treatment modalities have been topics of discussion in recent studies. Diagnosis is crucial, since lymphoma has a similar cytologic appearance and is more common in the elderly, but it differs in terms of both treatment and prognosis. We present a case of Ewing sarcoma in an octogenarian, in whom the findings on cytologic, histochemical, and cytogenetic examination facilitated accurate diagnosis and directed treatment.

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ewing's sarcoma ; octogenarians

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