A Detailed Examination of Retroperitoneal Undifferentiated Pleomorphic Sarcoma: A Case Report and Review of the Existing Literature

被引:1
|
作者
Balovic, Goran [1 ]
Stojanovic, Bojana S. [2 ,3 ]
Radovanovic, Dragce [1 ]
Lazic, Dejan [1 ]
Ilic, Milena [4 ]
Jovanovic, Ivan [3 ]
Svilar, Dejan [5 ]
Stankovic, Vesna [4 ]
Balovic, Jelena Sibalija [6 ]
Markovic, Bojana Simovic [3 ]
Stojanovic, Milica Dimitrijevic [3 ,4 ]
Jovanovic, Dalibor [4 ]
Stojanovic, Bojan [1 ,3 ]
机构
[1] Univ Kragujevac, Fac Med Sci, Dept Surg, Kragujevac 34000, Serbia
[2] Univ Kragujevac, Fac Med Sci, Dept Pathophysiol, Kragujavac 34000, Serbia
[3] Univ Kragujevac, Fac Med Sci, Ctr Mol Med & Stem Cell Res, Kragujevac 34000, Serbia
[4] Univ Kragujevac, Fac Med Sci, Dept Pathol, Kragujevac 34000, Serbia
[5] Univ Kragujevac, Fac Med Sci, Dept Radiol, Kragujevac 34000, Serbia
[6] Univ Clin Ctr Kragujevac, Dept Pediat, Kragujevac 34000, Serbia
关键词
retroperitoneal undifferentiated pleomorphic sarcoma; diagnostic challenges; therapeutic strategies; molecular pathogenesis; multidisciplinary treatment; targeted therapy; SOFT-TISSUE SARCOMA; MALIGNANT FIBROUS HISTIOCYTOMA; TERM-FOLLOW-UP; PROGNOSTIC-FACTORS; LONG-TERM; RADIATION-THERAPY; TAIL SIGN; CHEMOTHERAPY; ADJUVANT; RISK;
D O I
10.3390/jcm13133684
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
This detailed review focuses on retroperitoneal undifferentiated pleomorphic sarcoma (UPS), a particularly aggressive soft-tissue sarcoma that poses unique diagnostic and therapeutic challenges due to its rarity and complex presentation. By documenting a new case of retroperitoneal UPS and conducting a comprehensive review of all known cases, this article aims to expand the existing body of knowledge on the epidemiology, molecular pathogenesis, and treatment strategies associated with this rare disease. The complexity of diagnosing UPS is emphasized given that it rarely occurs in the retroperitoneal space and its histological and molecular complexity often complicates its recognition. This review highlights the need for specialized diagnostic approaches, including advanced imaging techniques and histopathological studies, to accurately diagnose and stage the disease. In terms of treatment, this paper advocates a multidisciplinary approach that combines surgery, radiotherapy and chemotherapy and tailors it to individual patients to optimize treatment outcomes. This review highlights case studies that illustrate the effectiveness of surgical intervention in the treatment of these tumors and emphasize the importance of achieving clear surgical margins to prevent recurrence. Furthermore, this review discusses the potential of new molecular targets and the need for innovative therapies that could bring new hope to patients affected by this challenging sarcoma.
引用
收藏
页数:17
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