A CASE OF RECTAL ENDOMETORIOSIS

In: The journal of the Japanese Practical Surgeon Society · 1991 · vol. 52(11) , pp. 2690–2693 · doi:10.3919/ringe1963.52.2690 · W2327071775
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This case report describes a rare instance of polypoid-grown endometriosis from the pouch of Douglas perforating the rectal wall in a 35-year-old female, leading to surgical resection after hormonal therapy failed.

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This case report describes a 35-year-old woman presenting with dysmenorrhea and bloody stool, who was diagnosed with rectal endometriosis after imaging revealed a walnut-sized filling defect. Despite five months of hormonal therapy failing to alleviate symptoms, surgical resection confirmed that endometrial tissue from the pouch of Douglas had penetrated the rectal wall, accompanied by an ovarian chocolate cyst. The authors note that this specific pattern of polypoid growth perforating the rectum is exceptionally rare, with only two similar cases previously reported in Japan. This paper is centrally about endometriosis — specifically a rare presentation of deep infiltrating endometriosis involving direct penetration of the rectal wall from the pouch of Douglas.

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Abstract

We report a case of intestinal endometriosis in which polypoid-grown endometrial tissues from the pouch of Douglas penetrated the rectal wall.A 35-year-old single female visited the hospital with the chief complaints of low abdominal pain during menstrual period and bloody stool. Barium enema showed a filling defect of walnut size and with irregular surface at the rectum. Endoscopic findings showed a cauliflower-like segmented tumor which was liable to bleed at the anterior wall of rectum. The endometrial tissue was confirmed with biopsy. Hormonal therapy for 5 months resulted in no synptomatic remission. Therefore, the anterior resection of the rectum was excised. The operative findings showed a close adhesion between the uterus and rectum, and a chocolate cyst at the right ovarium. Histological examination showed that endometrial tissue grown from the pouch of Douglas penetrated the rectal wall and protruded into the intestine. In addition, the endometrial tissue was observed at the right ovarium.Intestinal endometriosis commonly grows in the intestinal wall. It is rare, like this case, that endometriosis presenting polypoid-grown from the pouch of Douglas perforates the rectal wall, and only 2 cases have been reported in Japan.
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A CASE OF RECTAL ENDOMETORIOSIS 1991 Volume 52 Issue 11 Pages 2690-2693 Details Abstract We report a case of intestinal endometriosis in which polypoid-grown endometrial tissues from the pouch of Douglas penetrated the rectal wall. A 35-year-old single female visited the hospital with the chief complaints of low abdominal pain during menstrual period and bloody stool. Barium enema showed a filling defect of walnut size and with irregular surface at the rectum. Endoscopic findings showed a cauliflower-like segmented tumor which was liable to bleed at the anterior wall of rectum. The endometrial tissue was confirmed with biopsy. Hormonal therapy for 5 months resulted in no synptomatic remission. Therefore, the anterior resection of the rectum was excised. The operative findings showed a close adhesion between the uterus and rectum, and a chocolate cyst at the right ovarium. Histological examination showed that endometrial tissue grown from the pouch of Douglas penetrated the rectal wall and protruded into the intestine. In addition, the endometrial tissue was observed at the right ovarium. Intestinal endometriosis commonly grows in the intestinal wall. It is rare, like this case, that endometriosis presenting polypoid-grown from the pouch of Douglas perforates the rectal wall, and only 2 cases have been reported in Japan. A 35-year-old single female visited the hospital with the chief complaints of low abdominal pain during menstrual period and bloody stool. Barium enema showed a filling defect of walnut size and with irregular surface at the rectum. Endoscopic findings showed a cauliflower-like segmented tumor which was liable to bleed at the anterior wall of rectum. The endometrial tissue was confirmed with biopsy. Hormonal therapy for 5 months resulted in no synptomatic remission. Therefore, the anterior resection of the rectum was excised. The operative findings showed a close adhesion between the uterus and rectum, and a chocolate cyst at the right ovarium. Histological examination showed that endometrial tissue grown from the pouch of Douglas penetrated the rectal wall and protruded into the intestine. In addition, the endometrial tissue was observed at the right ovarium. Intestinal endometriosis commonly grows in the intestinal wall. It is rare, like this case, that endometriosis presenting polypoid-grown from the pouch of Douglas perforates the rectal wall, and only 2 cases have been reported in Japan. © Japan Surgical Association Favorites & Alerts Recently viewed articles

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endometriosis

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last seen: 2026-06-10T17:14:06.276822+00:00
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