Hepatic Angiomyolipoma: A Case Report and Review of the Literature

Jekaterina Strelčenko, J. Kuliavas, E. Stratilatovas, A. Dulskas
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Abstract

Background. Hepatic angiomyolipomas are uncommon non-cancerous mesenchymal tumors that belong to the perivascular epithelioid cell tumour group. Smooth muscle cells, fat cells and blood vessels can be observed in these types of neoplasm. Case presentation. We present the case of a 50-year-old patient. The patient was referred to the National Cancer Institute after an abdominal ultrasound, which incidentally revealed a mass in the liver. A whole body computed tomography scan showed a large liver mass, in the VII/VIII/V/VI segments. Trisegmenthomy of the right liver lobe was performed. Pathological examination revealed a rare, but benign tumour – angiomyolipoma. The postoperative course was uneventful and the patient was discharged on postoperative day 9. Two months following the surgery, the patient has no recurrence or late complications. Conclusion. Hepatic angiomyolipoma is a rare, usually benign tumour with malignant potential. It is can be diagnosed by radiological tests, biopsy or after surgery. The most common treatment is surgical resection.
肝血管肌脂肪瘤:病例报告和文献综述
背景。肝血管脂肪瘤是一种不常见的非癌间质肿瘤,属于血管周围上皮样细胞瘤。在这类肿瘤中可观察到平滑肌细胞、脂肪细胞和血管。病例介绍。我们介绍的是一名 50 岁患者的病例。患者在接受腹部超声波检查后,偶然发现肝脏内有肿块,随后被转诊至国家癌症研究所。全身计算机断层扫描显示,肝脏 VII/VIII/VVI 段有一个巨大肿块。患者接受了右肝叶三叶切除术。病理检查显示这是一种罕见的良性肿瘤--血管肌脂肪瘤。术后恢复顺利,患者于术后第 9 天出院。术后两个月,患者没有复发或晚期并发症。结论肝血管肌脂肪瘤是一种罕见的良性肿瘤,通常具有恶性潜能。可通过放射学检查、活组织检查或手术后确诊。最常见的治疗方法是手术切除。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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