Ito Shingo, Tachimori Yuji, Terado Yuichi, Sakon Ryota, Narita Kazuhiro, Goto Manabu
Department of Gastroenterological Surgery, Kawasaki Saiwai Hospital, 31-27 Omiyacho, Saiwai-ku, Kawasaki city, Kanagawa, 212-0014, Japan.
Department of Pathology, Kawasaki Saiwai Hospital, Kanagawa, Japan.
J Med Case Rep. 2021 May 5;15(1):237. doi: 10.1186/s13256-021-02821-6.
Primary malignant melanoma of the esophagus is a rare and aggressive disease that tends to have a poor response to chemotherapies. Previous studies have indicated that currently available treatment for primary malignant melanoma of the esophagus is insufficient. Here, we describe a case of recurrent primary malignant melanoma of the esophagus successfully treated with the immune checkpoint inhibitor nivolumab.
An 81-year-old Japanese female presented with a 3-month history of dysphagia. She was medicated for hypertension and sarcoidosis. The patient had no past history of cutaneous, ocular, or other-site melanomas. An esophagoscopy identified a 30-mm giant tumor in the lower esophagus, at a site 30 cm from the incisors. Enhanced computed tomography revealed wall thickening measuring 30 mm in size at the middle-third of the intrathoracic esophagus, with no significant lymph node infiltration or distant metastasis. Esophageal biopsy showed proliferation of large round tumor cells and melanophages. On the basis of these findings, the patient was diagnosed with esophageal malignant melanoma and underwent esophagectomy and lymph node dissection with gastric tube reconstruction. Although the pathological diagnosis was primary malignant melanoma of the esophagus, the patient presented with multiple lymph node and bone metastases 4 months after surgery. Subsequently, treatment with nivolumab 240 mg every 2 weeks was administered as the first-line treatment. Diffusion-weighted imaging with background body signal suppression following eight courses of nivolumab revealed that the multiple lymph node and bone metastases were markedly reduced. The patient received 30 courses of nivolumab and has maintained the partial response. No severe adverse events related to the immunotherapy were recorded.
The current study suggests that nivolumab may be a viable option for patients with metastatic primary malignant melanoma of the esophagus. Additional evidence from future clinical trials and research is necessary to fully validate these findings.
原发性食管恶性黑色素瘤是一种罕见且侵袭性强的疾病,对化疗往往反应不佳。既往研究表明,目前针对原发性食管恶性黑色素瘤的治疗方法并不充分。在此,我们报告一例复发性原发性食管恶性黑色素瘤患者,经免疫检查点抑制剂纳武单抗成功治疗。
一名81岁日本女性,有3个月吞咽困难病史。她患有高血压和结节病并正在接受治疗。该患者既往无皮肤、眼部或其他部位黑色素瘤病史。食管镜检查发现食管下段距门齿30 cm处有一个30 mm的巨大肿瘤。增强计算机断层扫描显示胸段食管中下段管壁增厚,大小为30 mm,无明显淋巴结浸润或远处转移。食管活检显示大圆形肿瘤细胞和黑色素巨噬细胞增殖。基于这些发现,患者被诊断为食管恶性黑色素瘤,并接受了食管切除术、淋巴结清扫术及胃管重建术。尽管病理诊断为原发性食管恶性黑色素瘤,但患者术后4个月出现多处淋巴结和骨转移。随后,每2周给予240 mg纳武单抗作为一线治疗。在接受8个疗程的纳武单抗治疗后,采用背景体素信号抑制的扩散加权成像显示,多处淋巴结和骨转移明显减少。该患者接受了30个疗程的纳武单抗治疗,并维持部分缓解状态。未记录到与免疫治疗相关的严重不良事件。
本研究提示,纳武单抗可能是转移性原发性食管恶性黑色素瘤患者的一个可行选择。未来还需要更多来自临床试验和研究的证据来充分验证这些发现。