Ichiyama Naruhiko, Yamane Hiromichi, Saitou Takako, Miura Masafumi, Mimura Ayaka, Kosaka Yoko, Kawahara Tatsuyuki, Nagasaki Yasunari, Ochi Nobuaki, Nakanishi Hidekazu, Fujiwara Hideyo, Takigawa Nagio
Department of General Internal Medicine 4, Kawasaki Medical School, Okayama, Japan.
Department of Pathology, Kawasaki Medical School, Okayama, Japan.
Thorac Cancer. 2025 Jun;16(11):e70098. doi: 10.1111/1759-7714.70098.
Malignant pleural mesothelioma (MPM) primarily progresses through direct invasion into the lung and pleura and is a refractory tumor in which asbestos exposure is a major underlying factor in most cases. Hematogenous metastasis of MPM is not uncommon in advanced stages, and reports suggest that metastatic sites may impact prognosis. Gastrointestinal metastases, ranging from the stomach to the colon, have been sporadically observed, but metastases to the small intestine and duodenum are exceedingly rare. Here, we report a case in which duodenal metastasis of MPM was endoscopically identified during the patient's lifetime while undergoing salvage chemotherapy following treatment with an immune checkpoint inhibitor and cytotoxic chemotherapy. Given the rarity and clinical significance of such cases, we present this report with a review of the relevant literature.
恶性胸膜间皮瘤(MPM)主要通过直接侵犯肺和胸膜进展,是一种难治性肿瘤,在大多数情况下,接触石棉是主要的潜在因素。MPM的血行转移在晚期并不少见,报告表明转移部位可能影响预后。从胃到结肠的胃肠道转移偶有观察到,但转移至小肠和十二指肠极为罕见。在此,我们报告一例MPM十二指肠转移病例,该病例在患者接受免疫检查点抑制剂和细胞毒性化疗后进行挽救化疗期间,通过内镜在其生前得以确诊。鉴于此类病例的罕见性及临床意义,我们撰写本报告并对相关文献进行综述。