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Case report: persistent double dorsal aorta
Paulo Henrique Alves Togni1, Ernani Alves de Oliveira1, Eduardo Milani Mora1
1Centro Universitário Padre Albino - UNIFIPA, Catanduva, SP, Brasil.
Persistent double dorsal aorta, an extremely rare congenital anomaly, was observed in a 79-year-old man presenting with limb pain. This embryological variant involved a split abdominal aorta and anomalous artery origin.
Area of Science:
- Vascular anatomy
- Embryology
- Congenital anomalies
Background:
- Persistent double dorsal aorta is an exceptionally rare congenital anomaly.
- Only 13 cases have been documented in existing literature.
Observation:
- This study details an embryological variant of the abdominal aorta.
- The observation was made in a 79-year-old male patient presenting with critical limb ischemia.
- The anomaly was identified via angiotomography.
Findings:
- Complete separation of the abdominal aorta into ventral and dorsal portions at the L3 vertebral level.
- The two aortic portions exhibited different calibers.
- An anomalous origin of the inferior mesenteric artery was also noted.
Implications:
- Highlights the importance of recognizing rare vascular variations in clinical practice.
- Contributes to the limited case series of persistent double dorsal aorta.
- May inform diagnostic approaches for patients with unexplained limb ischemia.
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