Background. Synovial sarcoma, a rare tumor in the head and neck, has b
een historically diagnosed by its characteristic biphasic histologic p
attern. Monophasic variants exist which can be difficult to diagnose.
Methods. Two cases of synovial sarcoma of the head and neck are presen
ted. In both cases, cytogenetic analysis was performed using standard
protocols. Results. Both tumors demonstrated a chromosomal translocati
on, t(X;18)(p11.2;q11.2), which either made or confirmed the diagnosis
. Conclusions. Synovial sarcoma contains a characteristic chromosomal
translocation which is a useful diagnostic teal, especially when histo
logic studies are equivocal. (C) 1997 John Wiley & Sons, Inc.