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A large retroperitoneal tumor with psoas infiltration: A rare case report

机译:伴有腰大肌浸润的大腹膜后肿瘤:罕见病例报告

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Context:Retroperitoneal sarcomas are rare neoplasms. Computed Tomography or Magnetic Resonance Imaging is performed in patients with these tumors to detect local extent and distant metastases of the tumor and for preoperative surgical planning. However the evaluation and treatment of retroperitoneal sarcomas are challenging because of its rarity and frequent presentation with advanced disease in an anatomically complex location.Case Report:We report a case of large retroperitoneal tumor in a female on the right flank. Ultrasound and Computed tomography scan of the abdomen revealed infiltration into the psoas muscle on the same side along with displacement of adjacent structures. Ultrasound guided fine needle aspiration cytology was suggested of liposarcoma. Surgical resection of the tumor was done. In follow up six months, patient was asymptomatic.Conclusions:In case of retroperitoneal tumors CT scan remains the diagnostic modality of choice and the inefficiency of adjuvant therapy; high recurrence rate and the very low chance of curing the patient after recurrence make the prognosis of these patients poor. However surgical resection remains the optimum treatment in all cases of retroperitoneal tumors.
机译:背景:腹膜肉瘤是罕见的肿瘤。对患有这些肿瘤的患者进行计算机断层扫描或磁共振成像,以检测肿瘤的局部范围和远处转移以及术前手术计划。然而,由于腹膜后肉瘤的稀有性和在复杂的解剖部位经常出现晚期疾病,因此评估和治疗腹膜肉瘤具有挑战性。病例报告:我们报告了一例右腹侧女性腹膜后大肿瘤的病例。腹部超声和计算机断层扫描显示,同侧的腰大肌浸润以及相邻结构的移位。超声引导细针穿刺细胞学检查提示脂肪肉瘤。进行了肿瘤的手术切除。结论:在腹膜后肿瘤的情况下,CT扫描仍是诊断的首选方式,且辅助治疗效率低下。复发率高,复发后治愈的机会很小,使这些患者的预后较差。然而,手术切除仍是所有腹膜后肿瘤的最佳治疗方法。

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