The cutaneous ciliated cyst (CCC) is a rarely reported lesion: only 21
cases have been reported since its first description by Clark in 1969
. The cyst occurs in genitally mature women in the lower part of the b
ody, mainly in the thigh and the buttock. It is lined with a ciliated
cuboidal epithelium that resembles tubal epithelium. Its connective ti
ssue contains no muscular fibers. CCC is considered as a heterotopia o
f the ducts of Muller. The authors report a new case of CCC situated i
n the buttock in a 17-year-old African girl. Histological examination
of the cyst revealed an association of ciliated cells and apocrine-loo
king cells. An immunohistochemical study of the cystic epithelial cell
s showed the presence of oestrogen and progesterone receptors which is
compatible with a Mullerian origin.