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

Author:

Balovic Goran1,Stojanovic Bojana S.23,Radovanovic Dragce1,Lazic Dejan1,Ilic Milena4ORCID,Jovanovic Ivan3ORCID,Svilar Dejan5,Stankovic Vesna4ORCID,Sibalija Balovic Jelena6,Markovic Bojana Simovic3,Dimitrijevic Stojanovic Milica34,Jovanovic Dalibor4,Stojanovic Bojan13ORCID

Affiliation:

1. Department of Surgery, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia

2. Department of Pathophysiology, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia

3. Center for Molecular Medicine and Stem Cell Research, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia

4. Department of Pathology, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia

5. Department of Radiology, Faculty of Medical Sciences, University of Kragujevac, 34000 Kragujevac, Serbia

6. Department of Pediatrics, University Clinical Center Kragujevac, 34000 Kragujevac, Serbia

Abstract

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.

Funder

Serbian Ministry of Science, Technological Development, and Innovation

Faculty of Medical Sciences at the University of Kragujevac, Serbia

Publisher

MDPI AG

Reference95 articles.

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3. Updates in Pathology for Retroperitoneal Soft Tissue Sarcoma;Mack;Curr. Oncol.,2022

4. Dellaire, G., Berman, J.N., and Arceci, R.J. (2014). Chapter 22—Soft Tissue Sarcomas. Cancer Genomics, Academic Press.

5. The evolving classification of soft tissue tumours—An update based on the new 2013 WHO classification;Fletcher;Histopathology,2014

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