Sen Chuah Jun, Yng Siaw Jia, Choon Soon Koon, Zamri Fatin Izni
Department of General Surgery, Pusat Perubatan Universiti Kebangsaan Malaysia, Kuala Lumpur, Malaysia.
Department of General Surgery, Hospital Sultanah Aminah, Ministry of Health Malaysia, Johor Bahru, Malaysia.
Ann Hepatobiliary Pancreat Surg. 2021 Aug 31;25(3):395-400. doi: 10.14701/ahbps.2021.25.3.395.
Primary hepatic liposarcoma is an extremely rare mesenchymal tumor that accounts for only 0.1% to 2% of primary malignant liver tumors. Due to its rarity, there is a lack of knowledge about its clinical course, management, and prognosis. Only 15 cases of primary liposarcoma of the liver have been reported since 1973. Among these 15 cases, only two involved primary liver liposarcoma with a pleomorphic subtype. Here we report the third and fourth cases of primary pleomorphic liver liposarcoma. A 57-year-old female presented with abdominal discomfort and progressive abdominal distension for two weeks. Computed tomography (CT) of her abdomen revealed a large well-defined solid nodule mass with an area of necrosis and hemorrhage occupying segment IV-B of the liver. Wide local excision was performed. She had an uneventful recovery and remained well at six months post-treatment. A 65-year-old male presented with an abdominal mass for two-month. CT demonstrated a mass in the left lobe of the liver with mixed soft tissues and fat attenuation. He underwent wide local excision. He was discharged on day three postoperatively. Histological analysis for both cases revealed liposarcoma of the liver with a pleomorphic subtype.
原发性肝脂肪肉瘤是一种极为罕见的间叶组织肿瘤,仅占原发性恶性肝肿瘤的0.1%至2%。由于其罕见性,人们对其临床病程、治疗方法及预后了解不足。自1973年以来,仅报道过15例原发性肝脂肪肉瘤病例。在这15例病例中,仅有两例为多形性亚型的原发性肝脂肪肉瘤。在此,我们报告第三例和第四例原发性多形性肝脂肪肉瘤病例。一名57岁女性因腹部不适及进行性腹胀两周前来就诊。其腹部计算机断层扫描(CT)显示肝脏IV - B段有一个边界清晰的巨大实性结节肿块,伴有坏死和出血区域。进行了广泛局部切除。她恢复顺利,治疗后六个月情况良好。一名65岁男性因腹部肿块两个月前来就诊。CT显示肝脏左叶有一个伴有软组织和脂肪衰减的肿块。他接受了广泛局部切除。术后第三天出院。两例病例的组织学分析均显示为多形性亚型的肝脂肪肉瘤。