Rebassa Llull M, Gutiérrez Sanz-Gadea C, Mus Malleu A, Muñoz Vélez D, Torralba Esteban J, Ozonas Moragues M
Servicio de Urología, Hospital Son Dureta, Palma de Mallorca, España.
Arch Esp Urol. 1999 Jan-Feb;52(1):78-80.
To describe an additional case of leiomyosarcoma of the kidney in a patient that presented with nonspecific abdominal pain and a palpable mass. The clinical features, diagnosis and therapeutic aspects, as well as the prognostic factors of this tumor type are reviewed.
Patient evaluation included US, CT and MRI. The patient underwent a left radical nephrectomy and received adjuvant external radiotherapy.
The patient is asymptomatic and has no local recurrence or metastasis 15 months postoperatively.
Leiomyosarcoma of the kidney is an uncommon malignant mesenchymal tumor. To our knowledge, less than 100 cases have been reported in the literature. Its clinical features and the US, CT and MRI findings are not unlike those of renal adenocarcinoma. The treatment of choice is by radical nephrectomy.
描述1例以非特异性腹痛和可触及肿块为表现的肾平滑肌肉瘤患者。回顾该肿瘤类型的临床特征、诊断、治疗方面以及预后因素。
对患者进行超声、CT和MRI评估。患者接受了左肾根治性切除术,并接受辅助外照射放疗。
患者无症状,术后15个月无局部复发或转移。
肾平滑肌肉瘤是一种罕见的恶性间叶肿瘤。据我们所知,文献报道不足100例。其临床特征以及超声、CT和MRI表现与肾腺癌无异。治疗的首选方法是根治性肾切除术。