Cheng An-Che, Lin Yi-Jia, Chiu Sung-Hua, Shih Yu-Lueng
Department of Internal Medicine, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
Department of Pathology, Tri-Service General Hospital, National Defense Medical Center, Taipei 114, Taiwan.
World J Clin Cases. 2021 Apr 16;9(11):2641-2648. doi: 10.12998/wjcc.v9.i11.2641.
Melanoma is uncommonly found in lymph nodes, subcutaneous tissue, or visceral organs without a primary lesion, where it is identified as metastatic melanoma with unknown primary (MUP). Hepatic MUP is extremely rare and has a poor prognosis. There is limited information on its pathogenesis, clinical and imaging features, and pathological findings. There are no guidelines for the use of immune checkpoint inhibitors (ICIs) in hepatic MUP, and the treatment outcome has rarely been reported.
A 42-year-old woman presented to our hospital with hepatic tumors found incidentally during a routine check-up. Contrast-enhanced abdominal com-puterized tomography showed multiple mass lesions in the liver. Pathological results revealed melanoma, which was confirmed by immunohistochemical staining for HMB-45(+), Melan-A(+), S-100(+), and SOX10(+). There was no evidence of primary cutaneous, ocular, gastrointestinal, or anal lesion on a comprehensive examination. The patient was diagnosed with hepatic MUP. She received combined antibodies against cytotoxic T-lymphocyte-associated antigen 4 (CTLA-4, ipilimumab) and programmed death protein-1 (PD-1, nivolumab). She died of hepatic failure 9 mo after hepatic MUP was diagnosed. This the first case of hepatic MUP treated with combined ipilimumab and nivolumab, who showed better outcome than previous cases.
Combined ICIs of PD-1 and CTLA-4 may be considered as the first-line therapy for patients with hepatic MUP.
黑色素瘤罕见于无原发灶的淋巴结、皮下组织或内脏器官,在此情况下被诊断为原发灶不明的转移性黑色素瘤(MUP)。肝MUP极为罕见,预后较差。关于其发病机制、临床及影像学特征和病理表现的信息有限。目前尚无肝MUP使用免疫检查点抑制剂(ICI)的指南,且治疗结果鲜有报道。
一名42岁女性因在常规体检中偶然发现肝脏肿瘤前来我院就诊。腹部增强计算机断层扫描显示肝脏有多个肿块病变。病理结果显示为黑色素瘤,通过HMB - 45(+)、Melan - A(+)、S - 100(+)和SOX10(+)的免疫组化染色得以证实。全面检查未发现原发性皮肤、眼部、胃肠道或肛门病变的证据。该患者被诊断为肝MUP。她接受了抗细胞毒性T淋巴细胞相关抗原4(CTLA - 4,伊匹单抗)和程序性死亡蛋白1(PD - 1,纳武单抗)的联合抗体治疗。在肝MUP诊断9个月后,她死于肝衰竭。这是首例用伊匹单抗和纳武单抗联合治疗的肝MUP病例,其治疗效果优于先前病例。
PD - 1和CTLA - 4联合ICI可考虑作为肝MUP患者的一线治疗方案。