Why the study?
Isolated iliac artery aneurysms are rare and usually asymptomatic until rupture, and their deep pelvic location makes clinical detection difficult.
Population
75-year-old man with a ruptured 60 × 50 mm saccular common iliac artery aneurysm
Design
Case report
Answers are grounded in this paper and cite their sources.
Should not yet change practice, though it supports vigilance for atypical urogenital symptoms; leaves open optimal screening and intervention thresholds for isolated iliac aneurysms.
Isolated iliac artery aneurysms are rare and usually asymptomatic until rupture, which carries a high mortality. Their deep pelvic location makes clinical detection difficult, and diagnosis is often incidental. We report the case of a 75-year-old man with insulin-treated type 2 diabetes and benign prostatic hyperplasia, in whom a pelvic CT scan incidentally revealed a giant iliac aneurysm. Initial examination found no pulsatile mass. During hospitalization, he developed abdominal pain, hematuria and hemorrhagic shock. Emergency CT angiography showed a partially thrombosed 60 × 50 mm saccular aneurysm of the common iliac artery with signs of rupture. He underwent emergency aortoiliac bypass with aneurysm exclusion and internal iliac artery ligation, but died in intensive care from refractory shock and multiorgan failure. This case highlights the high mortality of emergency repair compared with elective repair. Early detection and elective treatment of aneurysms larger than 3.5 to 4 cm, preserving internal iliac flow when feasible, are essential to improve outcomes.
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AKOUDAD et al. (2026) studied this question.
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