2
views
0
recommends
+1 Recommend
1 collections
    0
    shares
      • Record: found
      • Abstract: found
      • Article: found
      Is Open Access

      Late-stage primary renal angiosarcoma: an extremely rare cancer complicated by COVID-19 post-operatively

      case-report
      , ,
      Journal of Surgical Case Reports
      Oxford University Press

      Read this article at

      Bookmark
          There is no author summary for this article yet. Authors can add summaries to their articles on ScienceOpen to make them more accessible to a non-specialist audience.

          Abstract

          Primary renal angiosarcoma (AS) encompasses only 1% of soft tissue sarcomas, and it is seldom seen in literature. Because of its rarity, few risk factors for its development have been established. Due to lack of screening guidelines for kidney cancer, it is often found late when patients become symptomatic. We present the case of a male patient who presented with gross hematuria and flank pain and was discovered to have a large renal mass. Following successful resection, pathology showed it to be AS. The patient had a post-operative course complicated by two separate COVID-19 infections and expired 200 days after surgery. This case not only highlights an extremely rare renal cancer but also illustrates the challenges patients with complex medical issues faced in the era of COVID-19.

          Related collections

          Most cited references8

          • Record: found
          • Abstract: not found
          • Article: not found

          Guideline for management of the clinical T1 renal mass.

            Bookmark
            • Record: found
            • Abstract: found
            • Article: not found

            Angiosarcoma: clinical and imaging features from head to toe.

            Angiosarcoma is a rare, aggressive subtype of soft-tissue sarcoma with a propensity for local recurrence and metastasis associated with a generally poor prognosis, unless diagnosed early. Given the vascular endothelial cell origin of angiosarcoma, tumours may develop in essentially any organ; however, there is a predilection for the skin where half of all tumours arise, increasing in prevalence with age. The most common risk factors are chronic lymphoedema and history of radiation. We review the most important radiological findings along the spectrum of angiosarcoma from head to toe throughout the body, including uncommon and rare locations. Key imaging features of angiosarcoma across multiple organ systems will be described, as well as the impact on management and prognosis.
              Bookmark
              • Record: found
              • Abstract: found
              • Article: not found

              Primary renal angiosarcoma: a rare malignancy. A case report and review of the literature.

              Angiosarcoma is a rare malignant tumor occurring in less than 2% of soft tissue sarcomas. Angiosarcoma involving the kidney usually represents metastasis from skin or visceral primary lesions, while angiosarcoma primarily occurring in the kidney is a very rare neoplasm. In the English literature, from 1942 to the present, only 19 cases of primary kidney angiosarcoma have been reported. A case of primary renal angiosarcoma presenting as a large kidney mass and flank pain occurring after traumatism is reported. The present case represents further evidence of a rare malignancy.
                Bookmark

                Author and article information

                Contributors
                Journal
                J Surg Case Rep
                J Surg Case Rep
                jscr
                Journal of Surgical Case Reports
                Oxford University Press
                2042-8812
                December 2021
                24 December 2021
                24 December 2021
                : 2021
                : 12
                : rjab562
                Affiliations
                University of South Carolina School of Medicine , Columbia, SC, USA
                University of South Carolina School of Medicine , Columbia, SC, USA
                Department of Urology , Medical University of South Carolina, Florence, SC, USA
                Author notes
                Corresponding author. E-mail: Reilly.carr@ 123456uscmed.sc.edu
                Article
                rjab562
                10.1093/jscr/rjab562
                8711261
                e54b8d7d-8e94-4e44-b253-275af8106df8
                Published by Oxford University Press and JSCR Publishing Ltd. © The Author(s) 2021.

                This is an Open Access article distributed under the terms of the Creative Commons Attribution License ( https://creativecommons.org/licenses/by/4.0/), which permits unrestricted reuse, distribution, and reproduction in any medium, provided the original work is properly cited.

                History
                : 21 August 2021
                : 22 November 2021
                Page count
                Pages: 3
                Categories
                AcademicSubjects/MED00910
                jscrep/0170
                Case Report

                Comments

                Comment on this article