Paraovarian tumor of borderline malignancy: A case report.

Q4 Dentistry
Dimitrios Bairaktaris, Stefania Tsoplaktsoglou, Efthymia Souka, Konstantinos Kalmantis, Christos Iavazzo
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引用次数: 0

Abstract

Paraovarian tumors of borderline malignancy (PTBM) are exceedingly rare, with only slightly over 60 cases reported worldwide. This report presents the case of a 22-year-old nulliparous patient who incidentally discovered a left paraovarian mass during a routine abdominal ultrasound. Subsequent MRI revealed a 2.5×2.1 cm cystic lesion located in close proximity to, but outside of, the left ovary, with no other pathological findings. A laparoscopic cystectomy was performed with meticulous care to prevent tumor spillage, and the patient experienced an uneventful recovery. Histopathological examination unveiled irregularly shaped tissue measuring 2.2×1.2×1 cm, characterized by fibrous tissue/wall with spindle cell stroma and an epithelium displaying features consistent with a serous borderline tumor. Our multidisciplinary team recommended diligent follow-up. This case contributes to the existing literature on PTBM and highlights the imperative for additional cases to enhance our comprehension of the optimal management of these exceedingly rare tumors.

卵巢旁边缘恶性肿瘤:病例报告
卵巢旁恶性肿瘤(PTBM)极为罕见,全世界仅有略多于 60 例的报道。本报告所介绍的病例是一名 22 岁的无子宫患者,在一次常规腹部超声检查中偶然发现左侧卵巢旁肿块。随后的核磁共振检查发现一个 2.5×2.1 厘米的囊性病变,位于左卵巢附近,但不在左卵巢内,无其他病理发现。为防止肿瘤溢出,患者在小心翼翼的情况下接受了腹腔镜囊肿切除术,术后恢复顺利。组织病理学检查显示,肿瘤组织形状不规则,大小为 2.2×1.2×1 厘米,其特征是纤维组织/壁与纺锤形细胞基质和上皮显示出与浆液性边界肿瘤一致的特征。我们的多学科团队建议积极随访。该病例为现有的 PTBM 文献做出了贡献,同时也强调了我们需要更多的病例来提高我们对这些极为罕见的肿瘤的最佳治疗方法的理解。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Folia medica
Folia medica Medicine-Medicine (all)
CiteScore
1.00
自引率
0.00%
发文量
121
审稿时长
5 weeks
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