# Case report: full recovery from dialysis-requiring renal failure after surgical repair of a completely occluded renal artery in a patient with a single kidney

**Authors:** Marta Kantauskaite, Klaus Grabitz, Lars Christian Rump, Sebastian Alexander Potthoff

PMC · DOI: 10.1186/s12882-025-04352-4 · BMC Nephrology · 2025-08-01

## TL;DR

A patient with a single kidney and a completely blocked renal artery made a full recovery after surgery, thanks to preserved kidney function via collateral blood flow.

## Contribution

Highlights the importance of collateral circulation in preserving renal tissue viability in cases of complete renal artery occlusion.

## Key findings

- The patient showed moderate renal tissue perfusion despite total occlusion of the aorto-renal bypass.
- Collateral vasculature likely preserved kidney tissue oxygenation, enabling recovery after surgical repair.
- Evaluation of collateral perfusion is crucial in renal infarction cases with occluded main arteries.

## Abstract

Renal infarction is an extremely rare condition occurring in the context of structural or functional cardiac abnormalities, renal artery injury or coagulative syndromes. Although the clinical presentation of renal infarction is often nonspecific, the presence of symptoms such as back pain, high blood pressure, nausea and fever should raise suspicion, particularly in the emergency setting. Timely diagnosis is crucial for preserving renal function, whether through minimally invasive procedures or bypass surgery.

We present a case of a young male who developed acute occlusion of an aortic-renal bypass supplying a solitary left kidney. The patient exhibited resistant arterial hypertension and acute oligo-anuric kidney injury requiring dialysis. Despite the total occlusion of the aorto-renal bypass on imaging, doppler ultrasound demonstrated moderate renal tissue perfusion, likely maintained via collateral vasculature. The existence of a previous prolonged ischemic condition may have led to the formation of collateral-dependent circulation. While insufficient for pressure-dependent diuresis, the collateral flow preserved renal tissue oxygenation.

Collateral perfusion should be evaluated in cases of renal infarction, particularly when the main renal artery is occluded. Adequate collateral circulation might preserve renal tissue viability beyond the typical ischemic window.

## Full-text entities

- **Genes:** REN (renin) [NCBI Gene 5972] {aka ADTKD4, HNFJ2, RTD}, SH2D1A (SH2 domain containing 1A) [NCBI Gene 4068] {aka DSHP, EBVS, IMD5, LYP, MTCP1, SAP}
- **Diseases:** proteinuria (MESH:D011507), necrosis (MESH:D009336), Acute renal infarction (MESH:D056989), peripheral artery disease (MESH:D058729), renal artery injury (MESH:D000071079), anemia (MESH:D000740), cardio-embolic events (MESH:D000083262), bypass occlusion (MESH:D001157), hypertension (MESH:D006973), ischemic heart disease (MESH:D017202), hypercoagulability (MESH:D019851), hematuria (MESH:D006417), stenosis (MESH:D003251), back or flank pain (MESH:D021501), atrial fibrillation (MESH:D001281), ischemic (MESH:D002545), calcification (MESH:D002114), interventricular septal hypertrophy (MESH:D006984), drop in renal perfusion (MESH:D000094222), aneurysm (MESH:D000783), renal (MESH:D006030), nephrolithiasis (MESH:D053040), pyelonephritis (MESH:D011704), pain (MESH:D010146), pulmonary or peripheral edema (MESH:D011654), renal colic (MESH:D056844), back pain (MESH:D001416), coagulation (MESH:D001778), aorta (MESH:D000784), endocarditis (MESH:D004696), Renal infarction (MESH:D007238), RAS (MESH:D012078), nausea, vomiting (MESH:D020250), chronic ischemia (MESH:D007511), oligo-anuric renal failure (MESH:D051437), inflammation (MESH:D007249), abnormalities of heart valves (MESH:D006349), leukocytosis (MESH:D007964), nausea (MESH:D009325), thromboembolism (MESH:D013923), vomiting (MESH:D014839), renal graft thrombosis (MESH:D013927), artery dissection (MESH:D000094665), Acute renal ischemia (MESH:D058186), metabolic acidosis (MESH:D000138), arterial hypertension (MESH:D000081029), oxygen (MESH:D000860), FMD (MESH:D005352), hydronephrosis (MESH:D006869), atherogenic (MESH:D050197), fever (MESH:D005334), anuric kidney injury (MESH:D007674), coagulative syndromes (MESH:D025861), cardiac abnormalities (MESH:D018376)
- **Chemicals:** rivaroxaban (MESH:D000069552), Urea (MESH:D014508), aldosterone (MESH:D000450), creatinine (MESH:D003404), ePTFE (-), potassium (MESH:D011188), bicarbonate (MESH:D001639)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12317578/full.md

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Source: https://tomesphere.com/paper/PMC12317578