LEIOMYOSARCOMA
OF THE RENAL VEIN
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GUSTAVO C. LEMOS,
OMAR R. EL HAYEK, MARCELO APEZZATO
Albert Einstein
Jewish Hospital, São Paulo, SP, Brazil
ABSTRACT
Leiomyosarcoma
of the renal vein is a rare tumor of complex diagnosis. We presented a
case of renal vein leiomyosarcoma detected in a routine study. The primary
treatment was complete surgical removal of the mass. In cases where surgical
removal is not possible the prognosis is poor, with high rates of local
recurrence and distant spread.
Key words:
kidney; renal veins; muscle neoplasms; leiomyosarcoma
Int Braz J Urol. 2003; 29: 43-4
INTRODUCTION
There
are approximately 30 cases of leiomyosarcoma of the renal vein reported
in literature. They affect primarily the inferior vena cava in more than
50% of the cases (1). Pre-operative diagnosis is difficult due to its
low incidence, and since it presents a slow growing rhythm and nonspecific
symptoms. We present a case of primary leiomyosarcoma of the left renal
vein.
CASE REPORT
Patient
with 47 years, male, white came to the urologist to routine exam. In physical
examination identified a mass in left flank, painless and non mobile,
by palpation. An abdominal ultrasound showed a tumor without not related
to renal parenchyma and excretory route but in close contact with the
renal vein (Figure-1).
During the surgery we found that the tumor
had its origins in the renal vein and the patient was submitted to radical
left nephrectomy (Figure-2). The histological study disclosed renal vein
leiomyosarcoma.
DISCUSSION
Leiomyosarcoma
is an uncommon soft tissue tumor, generally occurring in myometrium, respiratory
tract and retroperitoneal organs. It seldom originates in vascular structures,
and the inferior vena cava responds for more than 50% of the cases (2).
Leiomyosarcoma of the inferior vena cava was first described in 1871 (1),
and its diagnosis and treatment is still challenging. These tumors attain
women over 30 years in 85% of the cases (2). More frequently they are
left-sided (64%). Symptoms are nonspecific, such as mild lumbar and abdominal
pain, and wasting. Hematuria and palpable mass are rare (2).
Until the 80s, approximately 50% of
the cases were autopsy findings. Presently they are incidentally found
in routine studies (2). Clinical context and ultrasound and computed tomography
studies are nonspecific and do not allow an adequate differential diagnosis
with other retroperitoneal solid tumors (3).
Leiomyosarcoma spread occurs primarily by
local extension. Through hematogenous spread it affects liver (25%), lungs
(63%), bones (19%) and, less frequently, lymph nodes (3). At diagnosis,
approximately half of the cases present metastatic disease or are nonresectable
due to local invasion, presenting therefore a poor prognosis (3).
The best treatment for leiomyosarcoma is
surgery with total tumor removal. This is the option that offers the best
chances of local control and 5 years survival. Studies performed at Memorial
Sloan Kettering, New York, showed that the major prognostic factor is
total surgical resection. When it is complete, 5 years survival free of
disease is of approximately 60%, vs. just 30 to 35% when it is partial.
Once total removal is performed, major prognostic factor becomes histological
grade, with 5 years free of disease survival of 90 to 95% for low grade
tumors, and of 30 to 35% for high grade tumors.
Radiotherapy and adjuvant chemotherapy have
limited effects due to toxicity on contiguous structures. Adjuvant therapy
is generally used to high grade tumors, with partial resection (3).
REFERENCES
- Bhathena
D, Vasquez M: Primary renal vein leiomyosarcoma. Cancer 1972; 30: 541-4.
- Brandes
SB, Chelsky MJ, Petersen RO, Greenberg RE: Leiomyosarcoma of the renal
vein. J Surg Oncol. 1996; 63: 195-200.
- Bevilacqua
RG, Rogatko A, Hadju SI, Brennan MF: Prognostic factors in primary retroperitoneal
soft-tissue sarcomas. Arch Surg. 1991; 126: 328-34.
______________________
Received:
August 12, 2002
Accepted after revision: January 9, 2003
________________________
Correspondence address:
Dr. Gustavo Caserta Lemos
Rua Jayme de Almeida Paiva, 81
São Paulo, SP, 05657-170, Brazil
Fax: + 55 11 3747-3333
E-mail: gclemos@ajato.com.br
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