Salemis Nikolaos S, Tsiambas Evangelos, Karameris Andreas, Tsohataridis Efstathios
2nd Department of Surgery, Army Veterans General Hospital, 10-12 Monis Petraki Str, 15121 Athens, Greece.
J Gastrointest Cancer. 2009;40(3-4):138-41. doi: 10.1007/s12029-009-9098-3.
Retroperitoneal liposarcoma is a rare tumor that may grow to a considerable size before causing clinical symptoms. Mixed-type retroperitoneal liposarcoma is a very rare clinical entity.
We herein describe a rare case of a 54-year-old female who was diagnosed with a giant retroperitoneal liposarcoma arising from the right perinephric space.
Radical nephrectomy and right salpingo-oophorectomy were necessary to achieve complete tumor excision. Histological examination revealed a mixed-type liposarcoma consisting of well-differentiated and pleomorphic elements and deep invasion into the renal parenchyma, which is quite infrequent. The patient was well and disease-free 12 months after surgery.
Mixed-type retroperitoneal liposarcoma is a rare tumor. Aggressive surgical resection of the tumor together with adjacent structures, if necessary, is the mainstay of treatment.
腹膜后脂肪肉瘤是一种罕见肿瘤,在引起临床症状之前可能生长到相当大的尺寸。混合型腹膜后脂肪肉瘤是一种非常罕见的临床实体。
我们在此描述一例罕见病例,一名54岁女性被诊断为起源于右肾周间隙的巨大腹膜后脂肪肉瘤。
为实现肿瘤完全切除,必须进行根治性肾切除术和右侧输卵管卵巢切除术。组织学检查显示为混合型脂肪肉瘤,由高分化和多形性成分组成,并深入侵犯肾实质,这种情况相当罕见。患者术后12个月情况良好且无疾病。
混合型腹膜后脂肪肉瘤是一种罕见肿瘤。如有必要,积极手术切除肿瘤及相邻结构是主要治疗方法。