Endometriose intestinal obstrutiva na pós-menopausa: relato de caso e revisão da literatura

In: instacron:APM · 2008 · W7120446971
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AI-generated summary by claude@2026-07, 2026-07-09

This case report and literature review describe a postmenopausal woman whose intestinal endometriosis mimicked a malignant lesion, leading to surgical intervention and recurrence.

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This paper reports a rare postmenopausal case of intestinal obstructive endometriosis and reviews the literature, describing a 74-year-old woman with hematochezia, tenesmus, liquid feces, and pelvic pain, but no other GI or gynecologic complaints. She had been postmenopausal for 22 years and previously had a panhysterectomy for endometrial thickening and an adnexal cyst; prior surgery for an acute obstructive abdomen revealed a small-bowel tumor mass, and pathology initially suggested endometriosis but was later revisited after later rectal biopsy showed endometrial-type mucosal fragments. Imaging and endoscopic findings simulated a malignant rectal lesion, and rectosigmoidectomy confirmed intestinal endometriosis; the patient later developed stenosing recurrence requiring colostomy. This paper is centrally about endometriosis — it focuses on postmenopausal intestinal (colorectal) obstructive endometriosis that mimicked malignancy.

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Abstract

CONTEXT: Endometriosis is characterized by the presence of endometrial tissue outside the uterine cavity, which is commonly detected in gynecological practice but rarely reported as a coloproctological disorder. The objective of the present report was to discuss a rare case of postmenopausal intestinal endometriosis simulating a malignant lesion, following a review of the literature. CASE REPORT: A 74-year-old woman with complaints of hematochezia and tenesmus of two months’ duration accompanied by liquid feces and pelvic pain, but with no other gastrointestinal or gynecological complaints, was referred to our service. She had been menopausal for 22 years, with no hormone replacement treatment, and had undergone panhysterectomy three years before the referral to us, due to endometrial thickening and a right adnexal cyst. Five months before this referral, she had undergone laparotomy due to acute obstructive abdomen, which revealed a tumor mass involving the small bowel. Anatomopathological examination of the enterectomy suggested a hypothesis of intestinal endometriosis. A proctological examination was normal. Computed tomography of the pelvis revealed thickening of the rectosigmoid transition and colonoscopy revealed friable tumor formation in the rectum. A biopsy of the lesion revealed mucosal fragments of endometrial type, which led to a review of the previous anatomopathological examination. The patient underwent rectosigmoidectomy with protective transversotomy, with a good postoperative course, and anatomical examination confi rmed the intestinal endometriosis. The patient subsequently suffered a stenosing recurrence of the lesion and has undergone colostomy since then.
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Keywords

Intestines, Endometriosis, Surgery, Diagnosis, PostmenopauseAbstract CONTEXT: Endometriosis is characterized by the presence of endometrial tissue outside the uterine cavity, which is commonly detected in gynecological practice but rarely reported as a coloproctological disorder. The objective of the present report was to discuss a rare case of postmenopausal intestinal endometriosis simulating a malignant lesion, following a review of the literature. CASE REPORT: A 74-year-old woman with complaints of hematochezia and tenesmus of two months’ duration accompanied by liquid feces and pelvic pain, but with no other gastrointestinal or gynecological complaints, was referred to our service. She had been menopausal for 22 years, with no hormone replacement treatment, and had undergone panhysterectomy three years before the referral to us, due to endometrial thickening and a right adnexal cyst. Five months before this referral, she had undergone laparotomy due to acute obstructive abdomen, which revealed a tumor mass involving the small bowel. Anatomopathological examination of the enterectomy suggested a hypothesis of intestinal endometriosis. A proctological examination was normal. Computed tomography of the pelvis revealed thickening of the rectosigmoid transition and colonoscopy revealed friable tumor formation in the rectum. A biopsy of the lesion revealed mucosal fragments of endometrial type, which led to a review of the previous anatomopathological examination. The patient underwent rectosigmoidectomy with protective transversotomy, with a good postoperative course, and anatomical examination confi rmed the intestinal endometriosis. The patient subsequently suffered a stenosing recurrence of the lesion and has undergone colostomy since then. Downloads

References

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