Pseudoaneurysm in the abdominal wall as a rare complication following surgery of a chronically superinfected urachal malformation — An exceptional case in congenital malformation surgery

Kugler A, Rompel O, Besendörfer M, Diez S (2025)


Publication Type: Journal article

Publication year: 2025

Journal

Book Volume: 127

Article Number: 110979

DOI: 10.1016/j.ijscr.2025.110979

Abstract

Introduction: A pseudoaneurysm, or aneurysma spurium, occurs due to a paravasal hematoma following a vascular injury. Pseudoaneurysms are extremely rare in children and adolescents. Because of the persistent blood flow through the supplying vessel, a potential rupture can cause life-threatening bleeding. Accurate diagnosis and treatment are therefore essential. Presentation of case: We present the case of an 11-month-old female infant with a congenital, exophytically growing, secreting tumor in the umbilical area. Surgical excision revealed a persistent urachus with a urachal cyst and a malformation on the bladder wall. Postoperatively, severe wound healing disorder developed, along with an intra-abdominal abscess. A pseudoaneurysm in the abdominal wall was incidentally detected with sonography, and CT confirmed perfusion from a branch of the right iliac artery. Initial catheter-based endovascular coiling was unsuccessful, and re-laparotomy for ligation, resection of the pseudoaneurysm, and debridement of the abscess was performed. The further course was complication-free. Discussion: Pseudoaneurysms, especially post-traumatic ones, can easily be misdiagnosed as a rare differential diagnosis in children and adolescents. Early diagnosis and interdisciplinary treatment are crucial for a successful outcome. Conclusion: In this particular case, it is assumed that the pseudoaneurysm developed as a result of chronic superinfection of the atypical urachal malformation.

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How to cite

APA:

Kugler, A., Rompel, O., Besendörfer, M., & Diez, S. (2025). Pseudoaneurysm in the abdominal wall as a rare complication following surgery of a chronically superinfected urachal malformation — An exceptional case in congenital malformation surgery. International Journal of Surgery Case Reports, 127. https://doi.org/10.1016/j.ijscr.2025.110979

MLA:

Kugler, Amelie, et al. "Pseudoaneurysm in the abdominal wall as a rare complication following surgery of a chronically superinfected urachal malformation — An exceptional case in congenital malformation surgery." International Journal of Surgery Case Reports 127 (2025).

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