M. Dealmeida et al., FINE-NEEDLE ASPIRATION BIOPSY OF CHILDHOOD RHABDOMYOSARCOMA - REEVALUATION OF THE CYTOLOGIC CRITERIA FOR DIAGNOSIS, Diagnostic cytopathology, 11(3), 1994, pp. 231-236
The distinction between rhabdomyosarcoma (RMS) and the other small rou
nd blue cell rumors of childhood has therapeutic implications which st
ress the importance of a correct diagnosis. In attempts to reevaluate
the cytologic criteria of this entity, we reviewed a series of 17 fine
-needle aspiration biopsies and three touch imprints from soft tissue
masses. AN cases had been histologically confirmed except for two case
s that only had immunocytochemical and ultrastructural confirmation. T
he features occurring most commonly include a uniform population of tu
mor cells arranged as single cells and cohesive aggregates. The cells
were predominantly round/polygonal, with uniform nuclei and scant to m
oderate amounts of cytoplasm. The nuclear chromatin was most often fin
ely granular and hyperchromatic, while nucleoli were inconspicuous. Bi
nucleated and multinucleated cells were found in 17 of the 20 smears.
Intracytoplasmic vacuoles were present in 17 cases, ranging from occas
ional in one case, a few in IO cases, and very numerous in six cases.
We conclude that the presence of bi/multinucleated cells is an importa
nt clue for the diagnosis of RMS on fine-needle aspiration biopsy. (C)
1994 Wiley-Liss, Inc.