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Multiple Renal Infarctions in Spontaneous Double Renal Artery Dissection: A Case Report
Gaetano Ferrara1, Michelangelo Nasuto2, Francesco Napolitano1
1Nephrology and Dialysis Unit, IRCCS Casa Sollievo Della Sofferenza Hospital, 71013 San Giovanni Rotondo, Italy.
Bilateral spontaneous renal artery dissection (SRAD) is an extremely rare condition. This case highlights diagnostic challenges and management of SRAD, emphasizing advanced imaging for accurate diagnosis.
Area of Science:
- Nephrology
- Vascular Surgery
- Radiology
Background:
- Spontaneous renal artery dissection (SRAD) is a rare cause of abdominal pain, with bilateral cases being exceptionally uncommon.
- Diagnosis is frequently delayed due to non-specific symptoms mimicking other conditions and the rarity of SRAD.
- Advanced imaging like CTA and MRA have improved diagnostic rates, including incidental findings.
Observation:
- Laboratory tests and radiological imaging revealed bilateral renal artery dissection.
- Multiple renal infarctions and ischemic areas were observed in both kidneys.
- The left renal artery showed intimal thickening and arteritis.
Findings:
- Multiplanar reconstruction confirmed bilateral renal artery dissection and widespread arterial infarctions.
- The patient was managed with dual antiplatelet therapy and ACE inhibitors following hypertension retargeting.
- No lipid-lowering therapy was required for this patient.
Implications:
- SRAD presents with varied symptoms and can be misdiagnosed, necessitating high clinical suspicion.
- Enhanced CT scans and vascular multiplanar reconstruction are crucial for accurate SRAD diagnosis.
- Despite over 300 reported cases, treatment consensus for SRAD remains elusive, with options including conservative management, open surgery, or endovascular intervention.
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