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

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Tác giả: Manuel Besendörfer, Sonja Diez, Amelie Kugler, Oliver Rompel

Ngôn ngữ: eng

Ký hiệu phân loại: 306.4846 Specific aspects of culture

Thông tin xuất bản: Netherlands : International journal of surgery case reports , 2025

Mô tả vật lý:

Bộ sưu tập: NCBI

ID: 497271

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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