Primary urachal leiomyosarcoma: a case report and literature review of clinical, pathological, and medical imaging features

Front Oncol. 2023 Aug 17:13:1228178. doi: 10.3389/fonc.2023.1228178. eCollection 2023.

Abstract

Background: Urachal tumors are exceedingly rare, and adenocarcinoma is the most common malignant urachal neoplasm. Here, an especially rare patient of primary urachal leiomyosarcoma from our hospital was reported, and only five patients have been reported thus far since 1981.

Case description: A 24-year-old man was admitted due to urinary tract symptoms. Both urogenital ultrasonography and contrast-enhanced computed tomography showed a mass at the dome of the urinary bladder. Laparoscopic surgical resection was performed, and histopathologic examination of the mass confirmed the diagnosis of urachal leiomyosarcoma. No recurrence was noted after one and a half years.

Conclusions: Because the leiomyosarcoma located in the extraperitoneal space of Retzius and may manifest with nonspecific abdominal or urinary symptoms, early and definitive preoperative diagnosis is challenging. Partial cystectomy with complete excision of the urachus is recommended. Because only a few patients have been recorded, clinical outcomes and recurrence risks are difficult to assess.

Keywords: case report; computed tomography; leiomyosarcoma; urachal tumor; urachus.

Publication types

  • Case Reports

Grants and funding

This study was supported by grants from the Sichuan Provincial Commission of Health (No. 19PJ284), the Science and Technology Association of Suining City (No. 6), and the Suining Central Hospital (Nos. 2021y09 and 2022ypj01).