Laparoscopic Minimally Invasive Approach for Pelvic Solitary Fibrous Tumor.

IF 3.4 2区 医学 Q2 ONCOLOGY
Annals of Surgical Oncology Pub Date : 2025-07-01 Epub Date: 2025-04-15 DOI:10.1245/s10434-025-17148-5
Claudio Lodoli, Andrea Rosati, Nazario Foschi, Francesco Santullo, Carlo Abatini, Miriam Attalla El Halabieh, Valerio Gallotta, Anna Fagotti, Fabio Pacelli
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Abstract

A solitary fibrous tumor (SFT) is a rare mesenchymal fibroblastic tumor characterized by intermediate behavior, with a peak incidence in the fifth and sixth decades of life. SFTs have been reported at almost every anatomic site, with approximately 20% of cases involving the abdominal cavity.1 SFTs are often asymptomatic and may be discovered as an incidental finding on imaging. Sometimes when the tumor size is large, it may produce symptoms related to pressure effects of adjacent organs.2 The standard treatment for SFTs consists of surgical resection with free resection margins. Given the rarity of SFTs, there is no global consensus for their treatment with respect to radiotherapy and adjuvant chemotherapy.3 A minimally invasive laparoscopic approach has been described in the literature, especially in cases where surgery is not extremely demolitive.4,5This report presents the case of a 66-year-old female with a preoperative diagnosis of SFT confirmed by percutaneous needle biopsy. A computed tomography scan showed a voluminous solid expansive formation in the pelvic area measuring 96 × 89 × 92 mm, which was attached to the ipsilateral ureter and was in contact with the internal iliac artery for over 180° (Tinelli's score grade 3). 6 The patient underwent surgery consisting of laparoscopic removal of the pelvic mass, with resection and re-implantation of the ipsilateral ureter and ligation of the internal iliac vessels. Video 1 provides a step-by-step description of the surgical strategy adopted. Minimally invasive surgery is feasible in selected patients with large mesenchymal tumors and could be a viable option for optimizing the multidisciplinary approach to treating this rare tumor.

腹腔镜微创入路治疗盆腔孤立性纤维性肿瘤。
孤立性纤维性肿瘤(SFT)是一种罕见的间充质纤维母细胞肿瘤,其特征为中间行为,发病率高峰发生在五六十岁。SFTs几乎在每个解剖部位都有报道,其中约20%的病例涉及腹腔SFTs通常无症状,可能是在影像学上偶然发现的。当肿瘤较大时,有时可产生与邻近器官压力作用有关的症状SFTs的标准治疗包括手术切除和自由切除边缘。鉴于SFTs的罕见性,对于其放疗和辅助化疗的治疗尚无全球共识微创腹腔镜方法已经在文献中描述,特别是在手术不是非常破坏性的情况下。4,5本报告报告一位66岁女性,术前经皮穿刺活检确诊为SFT。计算机断层扫描显示骨盆区有一个体积庞大的实性膨胀物,尺寸为96 × 89 × 92 mm,与同侧输尿管相连,与髂内动脉接触超过180°(Tinelli评分3级)。6患者接受腹腔镜下切除盆腔肿块,切除并重新植入同侧输尿管,结扎髂内血管。视频1提供了所采用的手术策略的逐步描述。微创手术在特定的大间充质肿瘤患者中是可行的,并且可能是优化多学科方法治疗这种罕见肿瘤的可行选择。
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
CiteScore
5.90
自引率
10.80%
发文量
1698
审稿时长
2.8 months
期刊介绍: The Annals of Surgical Oncology is the official journal of The Society of Surgical Oncology and is published for the Society by Springer. The Annals publishes original and educational manuscripts about oncology for surgeons from all specialities in academic and community settings.
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