Dr. Salomao et al., RHABDOMYOSARCOMA PRESENTING AS A PAROTID-GLAND MASS IN PEDIATRIC-PATIENTS - FINE-NEEDLE ASPIRATION BIOPSY FINDINGS, CANCER CYTOPATHOLOGY, 84(4), 1998, pp. 245-251
BACKGROUND, The head and neck region is one of the most common locatio
ns of rhabdomyosarcoma. Salivary gland involvement is usually secondar
y to advanced disease, and presentation as a primary salivary gland tu
mor is very rare. METHODS. Three cases of rhabdomyosarcoma presenting
as parotid masses, in 2 boys (ages 3 and 7 years) and a girl (age 5 ye
ars), were retrieved from the files of 2 institutions. RESULTS. The th
ree patients presented with parotid gland enlargement. Clinically, the
enlargements appeared to be inflammatory, and they were treated unsuc
cessfully with antibiotics. Fine-needle aspiration biopsy (FNAB) was p
erformed on all three patients. The cytologic features varied from one
case to another; one case had features of a small round cell tumor, a
nother was composed of a monomorphic population of spindle cells in a
metachromatic stroma, and the third case was composed mostly of spindl
e cells with moderate cellular pleomorphism. Immunohistochemical studi
es performed in two of the cases confirmed the diagnosis of rhabdomyos
arcoma, and ultrastructural studies were confirmatory in the other cas
e. The patients are alive; 2 of them have had no evidence of disease a
fter 6 and 9 years of follow-up, and the third, the most recent patien
t, has just finished adjuvant chemotherapy. CONCLUSIONS. With the incr
eased use of FNAB for the evaluation of salivary gland masses in child
ren, the authors believe that it is important to recognize the occurre
nce of rhabdomyosarcoma in this location. Immunohistochemical studies
have proved helpful in differentiating rhabdomyosarcoma from other par
otid gland tumors and can be readily done on cytologic preparations. C
ancer (Cancer Cytopathol) 1998;84:245-51. (C) 1998 American Cancer Soc
iety.