Primary pleomorphic liposarcoma of liver: a case report and review of the literature.
Primary pleomorphic liposarcoma of liver: a case report and review of the literature.
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DOI：
10.1155/2013/398910
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发表时间：
2013
影响因子：
--
通讯作者：
Kumar PV
中科院分区：
文献类型：
--
作者：
Naik PR;Kumar P;Kumar PV
原发性肝脏脂肪肉瘤是一种罕见的疾病。由于原发性肝脏脂肪肉瘤的罕见，对其临床病程、治疗和预后的了解都是有限的。先前已有12例原发性肝脏脂肪肉瘤的报告。我们报告第13例，发生在一名成年男性患者。一位42岁男性患者来我们门诊部就诊，主诉腹部疼痛、腹部肿块和体重减轻。超声检查显示肝左叶有一个肿块。腹部CT表现为肝左叶不均匀强化，多个囊性坏死区压迫胃、脾，无转移征象。鉴别诊断包括腺瘤和原发恶性肿瘤。均行剖腹探查和手术切除。HPE为肝脏多形性脂肪肉瘤。
Primary liver liposarcoma is a rare disease. The knowledge of the clinical course, management, and prognosis of primary liver liposarcoma are all limited because of its rarity. Twelve cases of primary liposarcoma of the liver have been previously reported. We present the thirteenth case, which occurred in an adult male patient. A 42-year-old male patient came to our outpatient department with complaints of pain abdomen, mass per abdomen, and weight loss. Ultrasonography showed a mass arising from the the left lobe of liver. CT abdomen showed a heterogenous enhancing mass from left lobe of liver with multiple cystic and necrotic areas compressing the stomach and spleen with no evidence of metastasis. Differential diagnosis included adenoma and primary malignancy. Exploratory laparotomy and resection were done. HPE was found to be pleomorphic liposarcoma of liver.