Authors
Hèla Ben Jmaà, Zied Ben Ayed, Faten Dhouib, Hafedh Daly, Rahma Kallel, Imed Frikha
Published in
Cardiovascular journal of Africa. Volume 37. Issue 4. Pages 454-457. Oct 16, 2026. Epub Oct 16, 2026.
Abstract
Vascular compression syndromes represent a group of rare conditions caused by extrinsic compression of veins or arteries by surrounding anatomical structures. These disorders are often underdiagnosed due to nonspecific symptoms, and the coexistence of multiple syndromes in a single patient is extremely rare. We report an 18-year-old woman with no past medical history who presented with intermittent abdominal and lumbar pain and progressive weight loss, without haematuria. Initial ultrasonography and contrast-enhanced computed tomography revealed the coexistence of Nutcracker, Dunbar (median arcuate ligament), and May-Thurner syndromes. The patient underwent open surgical management via median laparotomy, involving median arcuate ligament section to relieve coeliac trunk compression, transposition of the left renal vein, and decompression of the left common iliac vein by mobilisation of the right common iliac artery. The postoperative course was uneventful, with significant symptom relief and favourable long-term outcomes. This case highlights the diagnostic challenges and therapeutic complexity associated with combined vascular compression syndromes, emphasising the importance of a multidisciplinary surgical approach.
PMID:
42961838
Bibliographic data and abstract were imported from PubMed on 31 Oct 2026.
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