Evidence map›Paper›PMID 40505446›Full record

ArticleInternational journal of surgery case reports2025

A rare case of spontaneous aortic thrombosis presenting with unilateral auto-Lisfranc joint amputation in a young adult: A case report.

Ayto Addisu Negash, Amanuel Dagabas Wakoya, Dagmawi Anteneh Teferi, Hanna Tsehay Abebe, Rakeb Mulugeta Feyissa, Amanuel Mesfin Oljira

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Article in International journal of surgery case reports, 2025. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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6 authors.

Ayto Addisu NegashDepartment of Emergency Medicine and Critical Care, St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia. Electronic address: aytoaddisu19@gmail.com.
Amanuel Dagabas WakoyaDepartment of Emergency Medicine and Critical Care, St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
Dagmawi Anteneh TeferiDepartment of Surgery, St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
Hanna Tsehay AbebeDepartment of Internal Medicine, St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
Rakeb Mulugeta FeyissaDepartment of Emergency Medicine and Critical Care, St. Paul's Hospital Millennium Medical College, Addis Ababa, Ethiopia.
Amanuel Mesfin OljiraDepartment of General Surgery, Ambo University Referral Hospital, Oromia, Ethiopia.

Funding

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6 · The paper itself

Abstract

introduction and importanceSpontaneous aortic thrombosis is a rare clinical entity in young adults. Its rapid progression from intermittent claudication to critical limb ischemia presents significant diagnostic and therapeutic challenges. Early recognition and timely intervention are crucial to prevent severe complications. We report a rare case of spontaneous aortic thrombosis that presented with unilateral auto-Lisfranc joint amputation in a young adult. CASE PRESENTATION: A 22-year-old male presented with progressive intermittent claudication lasting five months, and a week's history of dark skin discoloration in both feet, leading to a left auto-Lisfranc joint amputation. Imaging studies revealed severe abdominal aortic thrombosis with absent blood flow to the lower extremities. Following this, an aorto-bifemoral bypass procedure was performed, resulting in an improved condition during discharge. CLINICAL DISCUSSION: This case underscores the atypical presentation of primary aortic thrombosis in a young adult with no identifiable risk factors. The striking occurrence of unilateral auto-Lisfranc joint amputation as the initial symptom is exceptionally rare. Imaging revealed extensive aortic thrombus without indications of vasculitis or an embolic source, thereby necessitating surgical revascularization.

conclusionEarly diagnosis and prompt intervention are crucial in preventing severe morbidity and limb loss related to acute limb ischemia. This case exemplifies the necessity for healthcare professionals to maintain heightened awareness of vascular diseases, particularly in young adults, and to act decisively to ensure optimal patient outcomes. Continuous follow-up, education on identifying symptoms of thromboembolism, and strict adherence to anticoagulation therapy are essential components in improving long-term prognosis and preventing recurrence.

Indexed as

Aortic thrombosisCase reportCritical limb ischemiaLisfranc joint amputationVascular diseaseYoung adult

Identifiers

PMID40505446
PMCPMC12182369

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