Vijay Adarsh, Ram Lakshmi
Departments of *General Surgery †Anaesthesiology, Hamad Medical Corporation, Doha, Qatar.
Am J Clin Oncol. 2015 Apr;38(2):213-9. doi: 10.1097/COC.0b013e31829b5667.
Retroperitoneal liposarcomas are rare mesenchymal tumors of the retroperitoneum that typically present with advanced disease and often carry a poor prognosis. Because of their rarity and anatomic location, these malignant tumors can cause a diagnostic dilemma and present several therapeutic challenges. They are usually associated with a high rate of recurrence despite grossly complete resection, thus requiring long-term and often indefinite follow-up. Relevant data on this topic was procured and synthesized with the aid of a comprehensive Medline search in addition to oncologic, pathologic, urologic, radiologic, and surgical literature review on retroperitoneal sarcomas. This article provides an in-depth review into the natural history, pathology, clinical manifestations, and prognostic features of retroperitoneal liposarcomas. It also discusses the reliability of diagnostic procedures and novel curative approaches that are currently being evaluated for the disease.
腹膜后脂肪肉瘤是一种罕见的腹膜后间充质肿瘤,通常在疾病晚期出现,预后往往较差。由于其罕见性和解剖位置,这些恶性肿瘤会导致诊断困境,并带来一些治疗挑战。尽管肉眼下完全切除,但它们通常复发率很高,因此需要长期且往往是不确定的随访。除了对腹膜后肉瘤进行肿瘤学、病理学、泌尿学、放射学和外科文献综述外,还借助全面的医学文献数据库检索获取并综合了关于该主题的相关数据。本文对腹膜后脂肪肉瘤的自然史、病理学、临床表现和预后特征进行了深入综述。它还讨论了诊断程序的可靠性以及目前正在针对该疾病评估的新型治疗方法。