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CASE REPORT article

Front. Oncol.

Sec. Pediatric Oncology

Case report: Urachal inflammatory myofibroblastic tumor with bladder invasion

Provisionally accepted
  • Capital Center For Children’s Health, Capital Medical University, Beijing, China

The final, formatted version of the article will be published soon.

Background: Urachal inflammatory myofibroblastic tumor (IMT) is a rare mesenchymal neoplasm characterized by non-specific clinical and imaging features, which renders it susceptible to clinical misdiagnosis. Complete surgical resection is the preferred treatment method. Case presentation: We herein report a case of urachal IMT in a 12-year-old male child who presented with dysuria for 4 days and abnormal urine color for 2 days. Preoperative ultrasonography and contrast-enhanced computed tomography (CT) both suggested an infected urachal cyst. Laparoscopic resection of the urachal mass was initially performed; however, intraoperative exploration identified bladder invasion by the mass, prompting an additional partial cystectomy. Postoperative histopathological examination confirmed the diagnosis of urachal IMT with bladder invasion. No adjuvant therapy was administered postoperatively, and the patient remained free of recurrence and metastasis during a 6-month follow-up period. Conclusion: In the differential diagnosis of pediatric urachal lesions, IMT should be considered, especially when adjacent tissue invasion is present. Enhanced understanding of urachal IMT can assist clinicians in the early recognition and precise management of this tumor.

Keywords: Anaplastic lymphoma kinase, Bladderinvasion, inflammatory myofibroblastic tumor, Surgery, Urachus

Received: 04 Jan 2026; Accepted: 09 Feb 2026.

Copyright: © 2026 Liu and Bai. This is an open-access article distributed under the terms of the Creative Commons Attribution License (CC BY). The use, distribution or reproduction in other forums is permitted, provided the original author(s) or licensor are credited and that the original publication in this journal is cited, in accordance with accepted academic practice. No use, distribution or reproduction is permitted which does not comply with these terms.

* Correspondence: Dongsheng Bai

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