Shibayama Ryo, Fujisawa Kentoku, Ogawa Yusuke, Shimoyama Hayato, Ohkura Yu, Honda Aya, Haruta Shusuke, Udagawa Harushi, Ueno Masaki, Takazawa Yutaka
Department of Gastroenterological Surgery, Toranomon Hospital, 2-2-2 Toranomon, Minato-Ku, Tokyo, 105-8470, Japan.
Department of Thoracic Surgery, Toranomon Hospital, 2-2-2 Toranomon, Minato-Ku, Tokyo, 105-8470, Japan.
Clin J Gastroenterol. 2025 Feb;18(1):29-36. doi: 10.1007/s12328-024-02050-6. Epub 2024 Oct 31.
Primary malignant melanoma of the esophagus is a rare disease with a poor prognosis. Surgical resection is common, but there is no consensus on perioperative treatment. Studies have reported the efficacy of programmed cell death-1 inhibitors (e.g., nivolumab, pembrolizumab) and anti-cytotoxic T-lymphocyte-associated antigen 4 agents (e.g., ipilimumab) in treating malignant melanoma. Here, we present the first case of primary malignant melanoma of the esophagus with lymph node metastases treated with nivolumab and ipilimumab followed by resection, achieving a pathologic complete response. A 75-year-old man presented with dysphagia. Esophagogastroduodenoscopy revealed a black, elevated lesion in the mid-thoracic esophagus. Biopsy confirmed primary malignant melanoma of the esophagus, showing tumor cells with melanin deposition, positive for HBM45 and S-100 staining. Computed tomography showed enlarged lymph nodes in the subclavian and mediastinum regions, suggesting metastases. After two courses of preoperative chemotherapy with ipilimumab and nivolumab, which significantly shrank the tumor, the patient underwent robot-assisted subtotal esophagectomy and 3-field lymph node dissection. Histopathological examination revealed no tumors or lymph node metastases, confirming a pathologic complete response. Given the rarity and poor prognosis of primary malignant melanoma of the esophagus, this case provides valuable insights for treatment strategies.
原发性食管恶性黑色素瘤是一种罕见疾病,预后较差。手术切除较为常见,但围手术期治疗尚无共识。研究报道了程序性细胞死亡蛋白1抑制剂(如纳武单抗、帕博利珠单抗)和抗细胞毒性T淋巴细胞相关抗原4药物(如伊匹木单抗)在治疗恶性黑色素瘤方面的疗效。在此,我们报告首例原发性食管恶性黑色素瘤伴淋巴结转移患者,先用纳武单抗和伊匹木单抗治疗,随后进行手术切除,实现了病理完全缓解。一名75岁男性因吞咽困难就诊。食管胃十二指肠镜检查发现胸段食管中部有一黑色隆起病变。活检确诊为原发性食管恶性黑色素瘤,肿瘤细胞有黑色素沉积,HBM45和S-100染色呈阳性。计算机断层扫描显示锁骨下和纵隔区域淋巴结肿大,提示有转移。在用伊匹木单抗和纳武单抗进行两个疗程的术前化疗使肿瘤明显缩小后,患者接受了机器人辅助食管次全切除术和三野淋巴结清扫术。组织病理学检查未发现肿瘤或淋巴结转移,证实为病理完全缓解。鉴于原发性食管恶性黑色素瘤的罕见性和预后较差,该病例为治疗策略提供了有价值的见解。