CASE 13819 Published on 04.08.2016

Asymptomatic left renal vein aneurysm with thrombosis

Section

Uroradiology & genital male imaging

Case Type

Clinical Cases

Authors

Tonolini Massimo, M.D.; Bazzi Luca Luigi, M.D.; Adriana Vella, M.D.

"Luigi Sacco" University Hospital,
Radiology Department;
Via G.B. Grassi 74
20157 Milan, Italy;
Email:mtonolini@sirm.org
Patient

64 years, female

Categories
Area of Interest Kidney ; Imaging Technique CT
Clinical History
A woman with history of chronic headache, hypertension and dyslipidaemia on medical treatment, presented to emergency department complaining of malaise, nausea and vague abdominal pain. Physical examination revealed low-grade fever, mild pelvic tenderness without peritonism. Routine laboratory assays were within normal limits for age.
Imaging Findings
Urgent multidetector CT (Fig. 1) did not confirm the clinical suspicion of acute diverticulitis or pyelonephritis, and detected a 1.5 cm well-demarcated roundish lesion with 15 Hounsfield Units precontrast attenuation, abutting the left renal vein. Multiplanar review of contrast-enhanced acquisition allowed to characterise the finding as saccular outpouching consistent with primary aneurysm of the renal vein, with internal nonenhancing thrombus which partially extended in the main venous lumen. No other abnormal findings were noted, particularly in the urogenital tract. Considering the absence of symptoms, vascular surgeons opted for surveillance, and the patient received antibiotics under diagnosis of uncomplicated urinary infection.
Repeated CT six months later (Fig. 2) showed unchanged size and morphology of the saccular venous aneurysm, with thin arterial-phase hyperenhancement surrounding the thrombus partially extending in the left renal vein. Further follow-up CT (Fig. 3) 18 months after initial diagnosis confirmed persistently stable venous aneurysm.
Discussion
A primary venous aneurysm (VA) is defined as a focal dilatation of a vein, which communicates with the main vessel through a single channel, in the absence of varicose veins, arterio-venous communication or pseudoaneurysm. Very uncommon compared to arterial aneurysms, VAs may be either developmental (probably from congenital weakness of elastic fibres in the venous wall) or acquired (secondary to trauma, inflammation or degenerative changes). Histologically, VAs retain the normal structure of the normal vein wall, with thinned elastic and muscular layers. Most VAs occur in the jugular, popliteal and saphenous veins. Albeit very uncommon, visceral VAs will be increasingly encountered due to the widespread use of cross-sectional imaging: among them, the majority involve the portal-mesenteric system (usually associated with portal hypertension) and inferior vena cava [1, 2].
Few (less than 20) cases of renal vein aneurysms (R-VAs) have been reported, in patients with a mean age of 52 years. While initial reports suggested that left-sided involvement was more frequent due to the greater length of renal vein, recent reviews did not confirm this side prevalence. Symptoms such as abdominal pain or haematuria are reported in less than 50% of patients. Therefore, R-VAs are often detected incidentally during surgery, ultrasound, CT or MRI studies [1-7].
Often sizeable (median 4-5 cm), R-VAs sonographically appear as anechoic oval or saccular-shaped lesions with internal slow venous flow. Cross-sectional imaging depicts fusiform or saccular structures in continuity and with synchronous contrast opacification with the renal vein. As this case exemplifies, partial or complete thrombosis represents the main complication, and is heralded by intraluminal CT hyperattenuation with corresponding filling defect in the venous post-contrast phase and peripheral “rim” enhancement. Occlusive thrombosis is reported in 13.6-23% of cases. Occasional cases of aneurismal rupture have been reported [1-7].
At CT differential diagnosis includes the normal variant represented by distended left renal vein, the possible “nutcracker” compression between aorta and superior mesenteric artery, splenic-renal shunt in the setting of portal hypertension, renal vein varicosities from congenital or acquired (generally iatrogenic) arterio-venous fistulization, arterial aneurysms, renal or pancreatic cystic lesions, and lymphadenopathy [3, 5, 7-9].
Symptomatic or complicated R-VAs require intervention with aneurysmectomy or aneurysmorraphy. Conversely, incidentally detected R-VAs may have limited clinical importance, and the therapeutic approach varies from “watchful waiting” using serial imaging follow-up in asymptomatic patients, to anticoagulation or endovascular stenting. Surgery is ultimately required in approximately one-half of patients [1-4].
Differential Diagnosis List
Partially thrombosed primary aneurysm of the left renal vein.
Non-thrombosed renal vein aneurysm
Distended left renal vein (normal variant)
Nutcracker phenomenon
Splenic-renal shunt in portal hypertension
Arterio-venous fistula
Renal artery aneurysm
Lymphadenopathy
Final Diagnosis
Partially thrombosed primary aneurysm of the left renal vein.
Case information
URL: https://www.eurorad.org/case/13819
DOI: 10.1594/EURORAD/CASE.13819
ISSN: 1563-4086
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