OBJECTIVE: To study the cytomorphologic features of the Ewing's sarcoma (ES
)family of tumors.
STUDY DESIGN: During a period of eight years (1990-1997), 123 soft tissue t
umors and 65 bone tumors were evaluated by fine needle aspiration cytology
(FNAC); 14 cases were diagnosed as in the ES family of tumors. The ages of
the patients ranged front 8 to 30 years. All the cases were histologically
confirmed.
RESULT: Of 14 cases of the ES family of tumors, 7 were neuroectodermal tumo
r (PPNET) and 2 Askin tumor. Cytologically, smears from all the cases showe
d round tumor cells with a high nuclear/cytoplasmic ratio. On detailed exam
ination, subtle differentiating features were observed. The cells in ES had
finer nuclear chromatin in comparison to those of PPNET and Askin tumor, a
nd punched-out clear cytoplasmic vacuoles were present. PPNET showed nuclea
r molding, unipolar cytoplasmic tags and Homer-Wright rosettes. Histologica
lly, all cases of ES and EOE and one case of Askin tumor showed periodic ac
id-Schiff-positive inclusions.
CONCLUSION: FNAC features coupled with clinical findings enable a rapid dia
gnosis of the ES family of tumors, from which treatment modalities can be d
etermined.