2012, Number 6
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Rev Mex Urol 2012; 72 (6)
Renal leiomyosarcoma
Zamora-Varela FR, Ponce-de León BF
Language: Spanish
References: 11
Page: 297-300
PDF size: 224.21 Kb.
ABSTRACT
Renal leiomyosarcoma is a rare and aggressive pathology that makes up 2% of renal tumors in the adult, presenting in the fifth and sixth decades of life. Diagnosis is made
through abdominal computerized tomography (CAT) or magnetic resonance imaging (MRI). Radical nephrectomy is the treatment of choice and outcome is poor.
A 32-year-old man presented with pain in the left renal fossa, gross hematuria, weight loss, and a palpable abdominal mass. CAT scan revealed a left renal tumor for which radical nephrectomy was performed. The histopathologic
study reported poorly differentiated leiomyosarcoma with a high grade of malignancy. Treatment based on chemotherapy and radiotherapy was successful.
Leiomyosarcomas are tumors of aggressive progression. Radical nephrectomy, which is the treatment of choice, plus adjuvant chemotherapy and radiotherapy is a therapeutic option.
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