Department of General, Visceral, and Transplantation Surgery, Ruprecht Karls University Hospital, Im Neuenheimer Feld 110, 69120, Heidelberg, Germany.
Liver Cancer Centre Heidelberg (LCCH), Heidelberg, Germany.
World J Surg Oncol. 2020 May 12;18(1):93. doi: 10.1186/s12957-020-01855-2.
Clinicopathological features and surgical outcomes of patients with fibrolamellar hepatocellular carcinoma (FL-HCC) are underreported. The aim of this study is to describe clinical characteristics and surgical outcomes for patients with this rare tumor to raise awareness among clinicians and surgeons.
Retrospective review of records of a tertiary referral center and specialized liver unit was performed. Out of 3623 patients who underwent liver resection, 366 patients received surgical treatment for HCC; of them, eight (2.2%) had FL-HCC and were resected between October 2001 and December 2018.
Eight patients (3 males and 5 females) with FL-HCC (median age 26 years) underwent primary surgical treatment. All patients presented with unspecific symptoms or were diagnosed as incidental finding. No patient had cirrhosis or other underlying liver diseases. Coincidentally, three patients (37.5%) had a thromboembolic event prior to admission. The majority of patients had BCLC stage C and UICC stage IIIB/IVA; four patients (50%) presented with lymph node metastases. The median follow-up period was 33.5 months. The 1-year survival was 71.4%, and 3-year survival was 57.1%. Median survival was at 36.4 months. Five patients (62.5%) developed recurrent disease after a median disease-free survival of 9 months. Two patients (25.0%) received re-resection.
FL-HCC is a rare differential diagnosis of liver masses in young patients. Since the prognosis is limited, patients with incidental liver tumors or lesions with suspicious features in an otherwise healthy liver should be presented at a specialized hepatobiliary unit. Thromboembolism might be an early paraneoplastic symptom and needs to be elucidated further in the context of FL-HCC.
纤维板层肝细胞癌(FL-HCC)的临床病理特征和手术结果报道较少。本研究旨在描述此类罕见肿瘤患者的临床特征和手术结果,以提高临床医生和外科医生的认识。
对一家三级转诊中心和专门的肝脏科进行了病历回顾性研究。在接受肝切除术的 3623 名患者中,有 366 名患者接受了 HCC 的手术治疗;其中 8 名(2.2%)患有 FL-HCC,并于 2001 年 10 月至 2018 年 12 月接受了手术切除。
8 名(3 名男性和 5 名女性)FL-HCC 患者(中位年龄 26 岁)接受了原发性手术治疗。所有患者均表现为非特异性症状或被诊断为偶然发现。没有患者患有肝硬化或其他基础肝病。巧合的是,3 名患者(37.5%)在入院前有血栓栓塞事件。大多数患者的 BCLC 分期为 C 期和 UICC 分期为 IIIB/IVA 期;4 名患者(50%)有淋巴结转移。中位随访期为 33.5 个月。1 年生存率为 71.4%,3 年生存率为 57.1%。中位生存时间为 36.4 个月。5 名患者(62.5%)在无疾病生存时间中位数为 9 个月后出现复发性疾病。2 名患者(25.0%)接受了再次切除。
FL-HCC 是年轻患者肝脏肿块的罕见鉴别诊断。由于预后有限,对于偶然发现的肝肿瘤或在健康肝脏中具有可疑特征的病变,应在专门的肝胆科就诊。血栓栓塞可能是早期副肿瘤症状,需要在 FL-HCC 的背景下进一步阐明。