A rare case of solitary fibrous pelvic tumor

L. Petrov, D. A. Golovkov, R. I. Moshurov, S. S. Malev, A. Fedenko
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Abstract

Non-organ retroperitoneal tumors are a heterogeneous group of malignant neoplasms that develop from different types of connective tissue, which in turn determines the variety of histological forms. More than 3,000 new cases of soft tissue sarcomas are registered an‑ nually in Russia, which is 1 % of all malignant neoplasms. In 2021, 3150 new cases of malignant neoplasms of connective and other soft tissues were detected for the first time. Retroperitoneal sarcomas account for 10–15 % of all types of soft tissue sarcomas. Diagnosis and treatment of non‑organ retroperitoneal tumors is an extremely difficult task. Non‑organ retroperitoneal tumors of mesenchymal origin are characterized by extremely rapid and aggressive growth. The prognosis of the disease is determined by the variant of the histological structure, the primary localization of the tumor, as well as timely and adequate treatment. Considering that non‑organ retroperitoneal tumors can metastasize to other organs in more than 30 % of cases, they are often detected at an advanced stage. Existing methods of radiation diagnostics and other research methods conducted within the framework of the examination standard, which can generally characterize the primary tumor of the retroperitoneal space, but in more than 60 % of cases give false positive information about the degree of tumor germination into neighboring organs and structures, especially into the main vessels. For this pathology, the main method of treatment is surgical. The long‑term results of surgical treatment and the expediency of palliative removal are currently insufficiently studied. Therefore, it is necessary to improve the methods of diagnosis and surgical treatment of non‑organ malignant tumors of the retroperitoneal space. Correct preoperative assessment of the prevalence and histological structure of the tumor allows you to choose an adequate amount of surgical intervention. This article presents a clinical observation of successful surgical treatment of a patient with solitary fibrous pelvic tumor.
孤立性骨盆纤维性肿瘤1例
非器官腹膜后肿瘤是一组异质性的恶性肿瘤,从不同类型的结缔组织发展而来,这反过来决定了组织学形式的多样性。俄罗斯每年新登记的软组织肉瘤病例超过3000例,占所有恶性肿瘤的1%。2021年,首次发现结缔组织和其他软组织恶性肿瘤3150例。腹膜后肉瘤占所有类型软组织肉瘤的10 - 15%。非器官腹膜后肿瘤的诊断和治疗是一项极其困难的任务。来源于间充质的非器官腹膜后肿瘤具有生长极快和侵袭性的特点。疾病的预后取决于组织结构的变异、肿瘤的原发部位以及及时、充分的治疗。考虑到非器官腹膜后肿瘤在30%以上的病例中可转移到其他器官,因此它们通常在晚期才被发现。现有的放射诊断方法等研究方法在检查标准的框架内进行,一般可以表征腹膜后间隙的原发肿瘤,但在60%以上的病例中,对肿瘤向邻近器官和结构,特别是向主血管的发芽程度给出假阳性信息。对于这种病理,主要的治疗方法是手术。手术治疗的长期结果和姑息性切除的便利性目前还没有充分的研究。因此,有必要改进腹膜后间隙非器官恶性肿瘤的诊断和手术治疗方法。正确的术前评估肿瘤的患病率和组织学结构可以让你选择适当数量的手术干预。本文报告一例孤立性骨盆纤维性肿瘤成功手术治疗的临床观察。
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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