类似晚期卵巢癌的息肉样子宫内膜异位症1例,快速生长、侵袭和传播。

IF 0.7 Q3 MEDICINE, GENERAL & INTERNAL
Hiroyuki Yazawa, Riho Yazawa, Kaoru Fukuda, Miki Ohara
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引用次数: 0

摘要

息肉样子宫内膜异位症是一种罕见的子宫内膜异位症,其特征是息肉样肿块,在组织学上通常类似于子宫内膜息肉。我们报告一例快速进展的息肉样子宫内膜异位症,术前认为是晚期卵巢癌。一位46岁女性,para 0,在给予促性腺激素释放激素(GnRH)激动剂4个月后,因子宫肌瘤和左侧卵巢子宫内膜囊肿行腹腔镜子宫肌瘤切除术和左侧附件切除术。术后11个月,右侧卵巢迅速增大。CT和MRI(均增强)显示右侧附件、盲肠、乙状结肠和大网膜肿块,PET-CT显示摄取增高,提示卵巢癌和腹膜播散。患者后来出现肠梗阻,结肠镜检查发现乙状结肠多发息肉样病变。剖腹探查时对大网膜肿瘤及右附件进行活检,经永久病理诊断为息肉样子宫内膜异位症,无恶性肿瘤。经GnRH拮抗剂治疗4个月后,右侧附件肿瘤明显缩小。第二次开腹手术行右附件肿瘤切除和回肠切除术。病理检查显示息肉样子宫内膜异位症从卵巢延伸至盲肠黏膜。患者术后1年多无症状。乙状结肠肿瘤缩小但仍存在。息肉样子宫内膜异位症主要影响卵巢、结肠、腹膜和网膜,患者年龄在四五十岁。它是一种良性疾病,但术前往往难以与恶性肿瘤区分,因为它迅速形成许多实性病变。虽然息肉样子宫内膜异位症是罕见的,没有特殊的影像学表现,包括它在鉴别诊断可能有助于术前识别。
本文章由计算机程序翻译,如有差异,请以英文原文为准。

A case of polypoid endometriosis mimicking advanced ovarian carcinoma with rapid growth, invasion, and dissemination.

A case of polypoid endometriosis mimicking advanced ovarian carcinoma with rapid growth, invasion, and dissemination.

A case of polypoid endometriosis mimicking advanced ovarian carcinoma with rapid growth, invasion, and dissemination.

A case of polypoid endometriosis mimicking advanced ovarian carcinoma with rapid growth, invasion, and dissemination.

Polypoid endometriosis is a rare form of endometriosis characterized by polypoid masses that histologically often resemble endometrial polyps. We report a case of rapidly progressing polypoid endometriosis that was preoperatively assumed to be advanced ovarian cancer. A 46-year-old woman, para 0, underwent laparoscopic myomectomy and left adnexectomy for uterine fibroids and a left ovarian endometrial cyst after administration of gonadotropin releasing hormone (GnRH) agonist for 4 months. Eleven months postoperatively, rapid right ovarian enlargement occurred. CT and MRI (both contrast-enhanced) showed masses in the right adnexa, cecum, sigmoid colon, and omentum, and PET-CT demonstrated increased uptake, suggesting ovarian cancer and peritoneal dissemination. The patient later developed intestinal obstruction, and colonoscopy revealed multiple polypoid lesions in the sigmoid colon. The omental tumor and right adnexa were biopsied during exploratory laparotomy, and diagnosed as polypoid endometriosis with no malignancy by permanent pathology. The right adnexal tumor shrunk markedly after 4 months of GnRH antagonist treatment. Second laparotomy was then performed for right adnexal tumor resection and ileocecectomy. Pathological examination revealed polypoid endometriosis extending from the ovary to the cecal mucosa. The patient has been asymptomatic for over 1 year postoperatively. The sigmoid colon tumor shrunk but is still present.Polypoid endometriosis predominantly affects the ovaries, colon, peritoneum, and omentum of patients in their 40s and 50s. It is a benign disease but is often difficult to distinguish from malignancy preoperatively because it rapidly forms numerous solid lesions. Although polypoid endometriosis is rare, with no specific imaging findings, including it in a differential diagnosis may facilitate preoperative identification.

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来源期刊
Fukushima Journal of Medical Science
Fukushima Journal of Medical Science MEDICINE, GENERAL & INTERNAL-
CiteScore
1.70
自引率
12.50%
发文量
24
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