INTRODUCTION
Angiomyolipoma is a nodule composed of variable
amounts of mature adipose tissue, smooth muscle, and
thick-walled blood vessels derived from perivascular
epithelioid cells usually arising in the renal cortex. Its
prevalence in the general population has been reported
to be 0,3-3% overall in the female patients (1). In the
multifocal form, it is usually associated to tuberous  scle-
rosis (2). The  average lesion size is from 2 mm to 20 cm
maximum diameter.  In most cases the angiomyolipoma
is asymptomatic and is diagnosed incidentally with
Ultrasound, CT and MRI done for other reasons. Renal
angiomyolipoma at times can be aggressive and may
show extension into renal vein and inferior vena
cava (3). We describe a paradigmatic case of a giant kid-
ney angiomyolipoma, not associated with tuberous scle-
rosis, invading the pelvis and the renal vein.

CASE REPORT
The lesion have been incidentally discovered in a 78 years
old woman by ultrasound scan done for other reasons.
Total body CT scan and MRI have been done showing large
node (18 mm) in the mediastinus, a 8 cm large lesion of the
upper pole of the left kidney with prevalence of fat tissue
and solid areas invading the renal vein for 4 cm, some large
nodes (1 cm) in the retroperitoneum and gallbladder
stones (Figure 1, 2). Past medical history included breast
reduction; hyatal hernia surgery; hypothiroidism; pulmu-

107Archivio Italiano di Urologia e Andrologia 2013; 85, 2

CASE REPORT

Renal angiomyolipoma with renal vein invasion

Francesca Di Cristofano, Federico Petrucci, Guglielmo Zeccolini, 
Genesio Leo, Calogero Cicero, Dario Del Biondo, Antonio Celia

Department of Urology, San Bassiano Hospital, Bassano del Grappa (VI), Italy.

Renal angiomyolipoma is a uncommon benign tumor, considered an hamartoma. The
lesion, usually benign, can be single or multiple and well-circumscribed. In letterature
only few cases of infiltrating angiomyolipomas have been described. The aim of the
paper is to describe a paradigmatic case of a giant kidney angiomyolipoma, not associ-
ated with tuberous sclerosis, invading the pelvis and the renal vein. The lesion have been

discovered incidentally during abdominal ultrasound for other pathology. Owing to the extent of
the lesion and the appreciable risk of bleeding, we opted for surgical treatment.

KEY WORDS: Angiomyolipoma; Kidney; Renal vein invasion; Radical nephrectomy.

Submitted 20 November 2012; Accepted 31 December 2012 No conflict of interest declared

Summary

nary infection during the last months. Blood tests:
Hb 15 g/dl-1 leukocyte 8 x 103  µl-1, urea 44 mg/d-1, cre-
atinine  0.9 mg/dl-1. The extension of the lesion, the risk
of bleeding and the risk of renal carcinoma were carefully
evaluated in order to decide the surgical treatment. The
patient underwent laparoscopic left adrenal sparing radical
nephrectomy. Definitive histology: renal angiomyolipoma
invading the renal vein with negative ilar nodes and normal
left renal parenchima (Figure 3, 4). No post-operative com-
plications. The patient was discharged in the fifth postop-
erative day.  At the first control, one month after the oper-
ation, the patient was asymptomatic, the abdominal ultra-
sound scan was normal and the blood tests were normal.

Figure 1.

Axial CT section
showing
extension 
of the lesion
into the 
renal vein.

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Archivio Italiano di Urologia e Andrologia 2013; 85, 2

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108

plex cases (7). Lesion larger than 4 cm may bleed, may
cause flank pain and may be palpable (8).  
When the lesion is growing, when it is symptomatic or
when the differential diagnosis is doubtful, surgical treat-
ment is necessary: enucleoresection, embolization or
radical nephrectomy (9).

CONCLUSIONS
In most cases angiomyolipoma is asymptomatic and it is
an incidental finding during Ultrasound scan or CT scan
done for other reasons. It may involve regional nodes,
renal vein or inferior vena cava, that can suggest an
aggressive evolution (10); anyway, these lesions are not
considered metastasis. In case of benign lesion the treat-
ment has to be conservative. Radical surgery is request-
ed in those rare cases where the angiomyolipoma is real-
ly large or involves the renal vein.

REFERENCES
1. Wagner BJ, Wong-you-Cheong JJ, Davis CJ. Adult renal hamar-
tomas. Radographics. 1997; 17:155-69.

2. Benanni S, Dahami Z, Dakir M, et al. Bilateral renal angiomy-
olipoma associated with tuberous sclerosis: report of a case. Ann
Urol. 2000; 34:278-282.

3. Bakshi SS, Vishal K, Kalia V, Gill JS. Aggressive renal angiomy-
olipoma extending into the renal vein and inferior vena cava - an
uncommon entity. Br J Radiol. 2011; 84:e166-e168.

4. Inomoto C, Umemura S, Sasaki Y, et al. Renal cell carcinoma aris-
ing in a long pre-existing angiomyolipoma. Pathol Int. 2007; 57:162-6.

5. Inci O, Kaplan M, Yalcin O, et al. renal angiomyolipoma with
malignant transformation, simultaneous occurrence with malignity
and other complex clinical situations. Int Urol Nephrol. 2006;
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6. Salerno S, Lo Casto A, Sorrentino F, et al. Bleeding Renal
Angiomyolipomas. Ct findings. Radiol Med. 2004; 107:229-33.

7. Pozzi Mucelli R, Locatelli M. diagnostica per immagini dell’an-
giomiolipoma renale: quadri tipici e atipici. Radiol Med. 2002;
103:474-87.

8. Steiner MS, Goldman SM, Fishman EK, Marshall FF. The natu-
ral history of renal angiomyolipoma. J Urol. 1993; 150:1782-1786.

9. Yiu WC, Chu SM, Collins RJ, et al. Aggressive renal angiomy-
olipoma: radiological and pathological correlation. JHK Coll Radiol.
2002; 5:240-2.

10. Wilson SS, Clark PE, Stein JP. Angiomyoplipoma with vena
caval extension. Urology. 2002; 60:695-6.

DISCUSSION
Renal angiomyolipoma is usually a benign lesion, it can be
rarely associated to renal adenocarcinoma (4, 5) and to
tuberous sclerosis. The histology shows mature adipose
tissue, smooth muscle, and thick-walled blood vessels.
The sporadic angiomyolipoma is monolateral and more
frequent in the females. When associated to tuberous scle-
rosis, angiomyolipomas are multiple, bilateral and larger. 
The clinical interest in angiomyolipoma is in its rapid
growth, the difficulty in distinguishing it from malignant
lesions, the difficulty of establishing the diagnosis and
correct treatment. 
The diagnosis is usually made by ultrasound scan that find
a hyperecogenic omogeneus lesion in the renal cortex.
The large lesions may have disomogeneus areas that make
the diagnosis difficult; TC scan is usually mandatory in the
large lesions: the diagnosis is based on the identification of
fat inside the lesion (6). MRI is useful only in some com-

Correspondence
Francesca Di Cristofano, MD (Corresponding Author)
Vico San Lorenzo 6 - Terni, Italy
fdicristofano@gmail.com

Federico Petrucci, MD
Guglielmo Zeccolini, MD
Genesio Leo, MD
Calogero Cicero, MD
Dario Del Biondo, MD
Antonio Celia, MD
Department of Urology San Bassiano Hospital 
Bassano del Grappa (VI), Italy

Figure 2.

T2 weighted
MRI mass

shows
hyperintense

signal 
with extension
into renal vein.

Figure 3.

Renal
angiomyolipoma:

blood vessels 
with thickened

walls mature
adipose tissue 

and smooth
muscle cells

mixed. EEx20

Figure 4.

Renal
angiomyolipoma:

renal vein
invasion. EEx5

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