卵巢囊腺纤维瘤及对侧碰撞性病变1例报告。

Oncoscience Pub Date : 2025-03-31 eCollection Date: 2025-01-01 DOI:10.18632/oncoscience.616
Naina Kumar, Ashutosh Rath, Aparna Setty, Pooja T Rathod, Jarathi Aparna
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摘要

卵巢囊腺纤维瘤是一种罕见的良性肿瘤,仅占卵巢良性肿瘤的1.7%。卵巢碰撞瘤更为罕见,碰撞瘤与其他良性卵巢肿瘤共存的情况极为罕见。本文报告一例独特的单侧卵巢浆液性囊腺纤维瘤,伴对侧卵巢浆液性和黏液性囊肿的碰撞特征。病例报告:一名41岁女性,下腹疼痛和肿胀持续2-3个月。腹部临床检查显示一个可移动、无压痛、囊性肿块,类似妊娠26-28周子宫,无游离液体。局部和镜内检查显示外阴、子宫颈和阴道健康,宫颈涂片上皮内病变或恶性肿瘤阴性。双侧检查发现可移动的多胎子宫和一个大的(约15 × 12厘米),主要是囊性病变,起源于右附件,向子宫的前方和上方延伸。核磁共振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,患者接受了探查性剖腹手术并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浆液性囊腺纤维瘤,左侧卵巢多发浆液性及黏液性囊肿,符合碰撞特征。子宫内膜增生,无异型性。结论:本病例强调了一侧卵巢良性表面上皮-间质瘤和另一侧卵巢碰撞特征的罕见共存。它强调了全面评估、精确诊断和及时手术管理的重要性,以确保最佳的患者预后。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Cystadenofibroma and contralateral collision lesions: A unique ovarian case report.

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.

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