Fetal rhabdomyoma is not generally considered part of nevoid basal cell carcinoma syndrome. However, a review of the literature revealed five patients with this syndrome who also had fetal rhabdomyomas in various locations. We report the first patient with nevoid basal cell carcinoma syndrome and a fetal rhabdomyoma of the tongue. We recommend that embryonal rhabdomyosarcoma be ruled out to avoid overly aggressive treatment of these patients.
GardnerDG, CorioRL. Fetal rhabdomyoma of the tongue, with a discussion of the two histologic variants of this tumor. Oral Surg Oral Med Oral Pathol1983;56:293–300.
3.
DiSant'AgnesePA, KnowlesDMII.Extracardiac rhabdomyoma: A clinicopathologic study and review of the literature. Cancer1980; 46:780–9.
4.
KapadiaSB, MeisJM, FrismanDM, Fetal rhabdomyoma of the head and neck: A clinicopathologic and immunophenotypic study of 24 cases. Hum Pathol1993;24:754–65.
5.
GorlinRJ, GoltzRW. Multiple nevoid basal-cell epithelioma, jaw cysts and bifid rib. A syndrome. N Engl J Med1960;262:908–12.
6.
ComptonJG, GoldsteinAM, TurnerM, Fine mapping of the locus for nevoid basal cell carcinoma syndrome on chromosome 9q. J Invest Dermatol1994;103:178–81.
7.
ShanleyS, RatcliffeJ, HockeyA, Nevoid basal cell carcinoma syndrome: Review of 118 affected individuals. Am J Med Genet1994;50:282–90.
EvansDG, LadusansRJ, RimmerS, Complications of the naevoid basal cell carcinoma syndrome: Results of a population based study. J Med Genet1993;30:460–4.
10.
HardissonD, Jiminez-HeffernanJA, NistalM, Neural variant of fetal rhabdomyoma and naevoid basal cell carcinoma syndrome. Histopathology1996;29:247–52.