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囊腺纤维瘤及对侧碰撞性病变:一例独特的卵巢病例报告

Cystadenofibroma and contralateral collision lesions: A unique ovarian case report.

作者信息

Kumar Naina, Rath Ashutosh, Setty Aparna, Rathod Pooja T, Aparna Jarathi

机构信息

Department of Obstetrics and Gynecology, All India Institute of Medical Sciences, Bibinagar, Hyderabad, Telangana 508126, India.

Department of Pathology, All India Institute of Medical Sciences, Bibinagar, Hyderabad, Telangana 508126, India.

出版信息

Oncoscience. 2025 Mar 31;12:26-33. doi: 10.18632/oncoscience.616. eCollection 2025.

Abstract

INTRODUCTION

Ovarian cystadenofibromas are rare benign tumors, accounting for only 1.7% of benign ovarian neoplasms. Even rarer are ovarian collision tumors, with the coexistence of collision tumors and other benign ovarian neoplasms being exceptionally uncommon. This report presents a unique case of serous cystadenofibroma in one ovary, accompanied by collision features involving serous and mucinous cysts in the contralateral ovary.

CASE REPORT

A 41-year-old woman presented with lower abdominal pain and swelling persisting for 2-3 months. Clinical evaluation of the abdomen revealed a mobile, non-tender, cystic mass resembling a 26-28-week gravid uterus, with no free fluid. Local and per speculum examinations showed a healthy vulva, cervix, and vagina, with a Pap smear negative for intraepithelial lesions or malignancy. A bimanual examination identified a mobile, multiparous uterus and a large (~15 × 12 cm), predominantly cystic lesion originating from the right adnexa and extending anteriorly and superiorly to the uterus. MRI findings confirmed these observations. Given the endometrial biopsy indicating endometrial intraepithelial neoplasia, the patient underwent an exploratory laparotomy with total abdominal hysterectomy and bilateral salpingo-oophorectomy. Histopathological analysis revealed serous cystadenofibroma in the right ovary and multiple serous and mucinous cysts in the left ovary, consistent with collision features. Additionally, the uterine endometrium showed hyperplasia without atypia.

CONCLUSION

This case underscores the rare coexistence of a benign surface epithelial-stromal tumor in one ovary and collision features in the other. It emphasizes the importance of comprehensive evaluation, precise diagnosis, and timely surgical management to ensure optimal patient outcomes.

摘要

引言

卵巢囊腺纤维瘤是罕见的良性肿瘤,仅占良性卵巢肿瘤的1.7%。更为罕见的是卵巢碰撞瘤,碰撞瘤与其他良性卵巢肿瘤并存的情况极为罕见。本报告介绍了一例独特的病例,一侧卵巢为浆液性囊腺纤维瘤,对侧卵巢伴有浆液性和黏液性囊肿的碰撞特征。

病例报告

一名41岁女性出现下腹部疼痛和肿胀,持续2 - 3个月。腹部临床检查发现一个可活动、无压痛的囊性肿块,类似妊娠26 - 28周的子宫,无游离液体。局部和窥器检查显示外阴、宫颈和阴道正常,巴氏涂片检查未发现上皮内病变或恶性肿瘤。双合诊检查发现子宫可活动、经产妇子宫,以及一个大的(约15×12 cm)、主要为囊性的病变,起源于右侧附件,向前上方延伸至子宫。磁共振成像(MRI)结果证实了这些观察结果。鉴于子宫内膜活检显示子宫内膜上皮内瘤变,患者接受了剖腹探查术,并行全腹子宫切除术和双侧输卵管卵巢切除术。组织病理学分析显示右侧卵巢为浆液性囊腺纤维瘤,左侧卵巢有多个浆液性和黏液性囊肿,符合碰撞特征。此外,子宫内膜显示增生但无异型性。

结论

本病例强调了一侧卵巢存在良性表面上皮 - 间质肿瘤,另一侧存在碰撞特征这种罕见的并存情况。它强调了全面评估、精确诊断和及时手术管理对确保患者获得最佳治疗效果 的重要性。

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