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. 2008 May 5:2:144.
doi: 10.1186/1752-1947-2-144.

Massive hematuria due to a congenital renal arteriovenous malformation mimicking a renal pelvis tumor: a case report

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Massive hematuria due to a congenital renal arteriovenous malformation mimicking a renal pelvis tumor: a case report

P Sountoulides et al. J Med Case Rep. .

Abstract

Introduction: Congenital renal arteriovenous malformations (AVMs) are very rare benign lesions. They are more common in women and rarely manifest in elderly people. In some cases they present with massive hematuria. Contemporary treatment consists of transcatheter selective arterial embolization which leads to resolution of the hematuria whilst preserving renal parenchyma.

Case presentation: A 72-year-old man, who was heavy smoker, presented with massive hematuria and flank pain. CT scan revealed a filling defect caused by a soft tissue mass in the renal pelvis, which initially led to the suspicion of a transitional cell carcinoma (TCC) of the upper tract, in view of the patient's age and smoking habits. However a subsequent retrograde study could not depict any filling defect in the renal pelvis. Selective right renal arteriography confirmed the presence of a renal AVM by demonstrating abnormal arterial communication with a vein with early visualization of the venous system. At the same time successful selective transcatheter embolization of the lesion was performed.

Conclusion: This case highlights the importance of careful diagnostic work-up in the evaluation of upper tract hematuria. In the case presented, a congenital renal AVM proved to be the cause of massive upper tract hematuria and flank pain in spite of the initial evidence indicating the likely diagnosis of a renal pelvis tumor.

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Figures

Figure 1
Figure 1
Axial computed tomography scan after intravenous administration of iodinated contrast material, arterial phase. A filling defect of soft tissue density is demonstrated within the right renal pelvis, which is also dilated. Differential diagnosis includes blood clot and tumor.
Figure 2
Figure 2
Selective digital subtraction arteriography of the right kidney showing an area of tortuous vascular channels located in the lower renal pole. The image taken a few seconds after the injection of contrast material demonstrates also early filling of the renal vein.
Figure 3
Figure 3
Image after transcatheter superselective embolization of the lesion with the use of coils. No vascular supply of the lesion is demonstrated.

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