Takada Ryuji, Takahashi Makoto, Hayashi Tatsuya, Higashihara Taku, Morita Yasuhiro, Inoue Dai, Okada Haruka, Araki Junko
Department of Surgery, Tokyo Metropolitan Tama Medical Center, Tokyo 183-8524, Japan.
Department of Gastroenterology and Hepatology, Tokyo Metropolitan Tama Medical Center, Tokyo 183-8524, Japan.
Biomed Rep. 2024 Aug 23;21(5):154. doi: 10.3892/br.2024.1842. eCollection 2024 Nov.
Li-Fraumeni syndrome (LFS) is a hereditary cancer predisposition syndrome associated with germline mutations in tumor suppressor gene . Perivascular epithelioid cell tumors (PEComas) are a group of tumors by the World Health Organization Classification as mesenchymal tumors composed of histologically and immunohistochemically distinctive PECs. The present study reports a rare case of PEComa associated with LFS. A 32-year-old female patient was referred to Tokyo Metropolitan Tama Medical Center (Tokyo, Japan) in March 2022 for a detailed examination of a liver mass. The patient had received a diagnosis of LFS based on a history of sarcoma and germline variants of 7 years previously. Magnetic resonance imaging revealed a ring-enhanced mass in the liver segment 8 (S8). This was observed in the arterial phase, followed by washout of contrast media in the venous phase. Owing to the possibility of malignancy (such as metastatic liver tumor or hepatocellular carcinoma), the patient was referred for diagnostic surgery. In August 2022, a laparoscopic partial hepatectomy of S8 was performed without complications and she was discharged on postoperative day 7. The pathological findings led to the diagnosis of PEComa. The patient is currently under follow-up at 1 year and 4 months postoperative. Laparoscopic hepatectomy was useful as a diagnostic treatment because it was relatively non-invasive. Mutations in are involved in the development of PEComa. Further cases and studies are required to clarify the relationship between LFS and PEComa.
李-弗劳梅尼综合征(LFS)是一种遗传性癌症易感性综合征,与肿瘤抑制基因的种系突变有关。血管周上皮样细胞瘤(PEComas)是世界卫生组织分类中的一组肿瘤,属于间充质肿瘤,由组织学和免疫组化上独特的周上皮样细胞(PECs)组成。本研究报告了一例罕见的与LFS相关的PEComa病例。一名32岁女性患者于2022年3月被转诊至东京都多摩医疗中心(日本东京),对肝脏肿块进行详细检查。该患者基于7年前的肉瘤病史和种系变异被诊断为LFS。磁共振成像显示肝段8(S8)有一个环形强化肿块。在动脉期观察到这种情况,随后在静脉期造影剂消退。由于存在恶性肿瘤的可能性(如肝转移瘤或肝细胞癌),该患者被转诊进行诊断性手术。2022年8月,对S8进行了腹腔镜肝部分切除术,无并发症发生,患者于术后第7天出院。病理结果诊断为PEComa。该患者目前在术后1年4个月接受随访。腹腔镜肝切除术作为一种诊断性治疗方法很有用,因为它相对无创。 中的突变与PEComa的发生有关。需要更多病例和研究来阐明LFS与PEComa之间的关系。