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NDT Advance Access originally published online on August 24, 2004
Nephrology Dialysis Transplantation 2005 20(2):460-461; doi:10.1093/ndt/gfh482
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Nephrol Dial Transplant Vol. 20 No. 2 © ERA–EDTA 2005; all rights reserved


Images in Nephrology
(Section Editor: G. H. Neild)

Nutcracker syndrome and left unilateral haematuria

Chiz-Tzung Chang1, Cheng-Chieh Hung1, Koon-Kwan Ng2 and Tzung-Hai Yen1,3

1 Department of Nephrology, Chang Gung Memorial Hospital, Taipei, 2 Department of Radiology, Chang Gung Memorial Hospital, Keelung, Taiwan and 3 Histopathology Unit, Cancer Research UK, London Research Institute, London, UK

Correspondence and offprint requests to: Tzung-Hai Yen, MD, Department of Nephrology, Chang Gung Memorial Hospital, 199, Tung Hwa North Road, Taipei 105, Taiwan. Email: m19570{at}adm.cgmh.org.tw

Keywords: nutcracker syndrome; haematuria; magnetic resonance angiography

The nutcracker phenomenon refers to compression of the left renal vein between the aorta and superior mesenteric artery. This phenomenon with its associated symptoms and signs is defined as nutcracker syndrome [1]. It occurs in relatively young and previously healthy people. The compression leads to left renal vein hypertension, which may result in rupture of the thin walled vein into the renal calyceal fornix with the clinical presentation of intermittent gross or microscopic haematuria. There can also be collateral venous circulation formation such as a prominent left ovarian vein or testicular vein with its associated symptoms, such as vulvar varices in females or varicoele in males [2].

A 37-year-old female was referred to our hospital with a 3 year history of symptoms of intermittent gross haematuria and painful left flank. Her past medical and family histories were normal. All blood tests including complete blood cell count, biochemistry, blood clotting profile, serum immunoglobulin electrophoresis and antinuclear antibody were within normal limits. Urinary analysis revealed numerous red blood cells without dysmorphic changes. Renal ultrasound was also normal. Magnetic resonance imaging revealed a dilated left renal vein after passing between the aorta and superior mesenteric artery (Figure 1a). Magnetic resonance angiography (MRA) showed that the diameter of the left renal vein was larger in the left part adjacent to the aorta compared with the right adjacent part. A prominent left ovarian vein, implicating formation of a collateral circulation, was also noted (Figure 1b). Digital subtraction MRA found the impingement of the left renal vein between the aorta and superior mesenteric artery (Figure 1c). Nutcracker syndrome was diagnosed by the combination of clinical and MRA findings. The patient received no surgical treatment and has remained stable over the subsequent 3 years.



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Fig. 1. (a) MRI revealed a dilated left renal vein (black arrows) after passing between the aorta (A) and superior mesenteric artery (white arrowhead). (b) MRA showed that the diameter of the left renal vein (black arrow) was larger in the left part adjacent to the aorta (A) compared with the right adjacent part. A prominent left ovarian vein (white arrow), implicating formation of a collateral circulation, was also noted. IVC = inferior vena cava. (c) Digital subtraction MRA found the impingement of the left renal vein (LRV) between the aorta (A) and superior mesenteric artery (white arrowhead).

 
The diagnosis of nutcracker syndrome is primarily by imaging, and can sometimes be difficult. Nevertheless, treatment of this syndrome is still controversial [1]. The main indication for surgery is severe persistent or recurrent haematuria that has caused anaemia and ureteral passage of blood clots causing abdominal or flank pain.

Conflict of interest statement. None declared.

References

  1. Kim SH, Cho SW, Kim HD, Chung JW, Park JH, Han MC. Nutcracker syndrome: diagnosis with Doppler US. Radiology 1996; 198: 93–97[Abstract/Free Full Text]
  2. Wendel RG, Crawford ED, Hehman KN. The ‘nutcracker’ phenomenon: an unusual cause for renal varicosities with hematuria. J Urol 1980; 123: 761–763[Web of Science][Medline]

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