# Left Renal Artery Thrombosis in a Patient With von Willebrand Disease Type 3 and Factor V Leiden Heterozygosity

**Authors:** Natalie L Albright, Sana Kamboj, Jason M Lucas

PMC · DOI: 10.7759/cureus.94029 · Cureus · 2025-10-07

## TL;DR

A rare case of a man with severe bleeding disorder and a blood clotting condition developed a rare arterial clot in his kidney.

## Contribution

First reported case of VWD type 3 combined with FVL causing arterial thrombosis.

## Key findings

- A patient with VWD type 3 and FVL heterozygosity developed left renal artery thrombosis.
- This case highlights the possibility of arterial thrombosis in severe bleeding disorders.
- Treatment considerations for such combined disorders are not well documented.

## Abstract

There are a few cases of combined thrombotic and hemophilic disorders coexisting in patients that have been published in the literature, such as factor V Leiden (FVL) with von Willebrand disease (VWD) type 1, and a report of a patient with VWD type 3, protein C and antithrombin III deficiency, and venous thromboses, but no reports in the literature were found of a patient with VWD type 3 and FVL and arterial thromboses. VWD type 3 is the most severe form because it results in nonexistent levels of von Willebrand factor (VWF) and is believed to be protective against arterial thromboses. We present a unique case of a 41-year-old man with a known history of VWD type 3 who presented with left renal artery thrombosis and a large left renal infarct, who was subsequently diagnosed with FVL heterozygosity. Both FVL and VWD type 3 can coexist in a patient. These patients require special considerations in treatment that have not been well documented throughout the literature.

## Linked entities

- **Proteins:** SERPINC1 (serpin family C member 1)
- **Diseases:** von Willebrand disease type 3 (MONDO:0010191)

## Full-text entities

- **Genes:** F5 (coagulation factor V) [NCBI Gene 2153] {aka FVL, PCCF, RPRGL1, THPH2, fV}, PROC (protein C, inactivator of coagulation factors Va and VIIIa) [NCBI Gene 5624] {aka APC, PC, PROC1, THPH3, THPH4}, VWF (von Willebrand factor) [NCBI Gene 7450] {aka F8VWF, VWD}
- **Diseases:** left renal infarct (MESH:D007238), antithrombin III deficiency (MESH:D020152), thrombotic (MESH:D013927), hemophilic disorders (MESH:D009358), von Willebrand disease (VWD) type 1 (MESH:D056725), arterial thromboses (MESH:D002341), VWD type 3 (MESH:D056729), venous thromboses (MESH:D020246), Left Renal Artery Thrombosis (MESH:D012078)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Full text

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## Figures

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## References

11 references — full list in the complete paper: https://tomesphere.com/paper/PMC12591350/full.md

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Source: https://tomesphere.com/paper/PMC12591350