We report a unique case of rectal endometriosis mimicking solitary rec
tal ulcer syndrome. Several rectal biopsies were performed before the
correct diagnosis of rectal endometriosis was made. The lesion had str
iking histologic features resembling colitis cystica profunda. The pre
sence of two types of glands, i.e., colonic glands with marked depleti
on of mucin and endometrial glands, were readily apparent on immunohis
tochemical stain using anticarcinoembryonic antigen showing positive c
ytoplasmic stain for colonic glands but negative for endometrial gland
s. However, the distinction between colonic and endometrial glands was
very difficult on hematoxylin-and-eosin-stained slides. Endometrial s
troma was identified only in the sixth biopsy specimen. Although rare,
rectal endometriosis should be considered in the differential diagnos
is of solitary rectal ulcer syndrome.