Kubo Kentaro, Oguma Junya, Utsunomiya Daichi, Kanematsu Kyohei, Fujii Yusuke, Kurita Daisuke, Ishiyama Koshiro, Abe Seiichiro, Sekine Shigeki, Daiko Hiroyuki
Esophageal Surgery Division, National Cancer Center Hospital, Tokyo, Japan.
Endoscopy Division, National Cancer Center Hospital, Tokyo, Japan.
Case Rep Gastroenterol. 2022 Nov 2;16(3):569-576. doi: 10.1159/000526749. eCollection 2022 Sep-Dec.
Esophageal carcinosarcoma (EC) is a rare malignant tumor, accounting for 0.5-2.8% of esophageal cancers. Most are advanced cancers that are detected as polypoid lesions and are treated with multidisciplinary therapy with a focus on surgery. However, endoscopic findings, pathological findings, and long-term outcomes of early-stage EC are often unclear because there are very few reported cases. This paper reports three cases of EC confined to the mucosal layer. The macroscopic type of all tumors was polypoid lesion with a slightly depressed lesion. All cases were clinically diagnosed as invasive cancer before treatment. Pathological diagnosis of tumor depth showed that one case had invaded the lamina propria mucosae, and two cases had invaded the muscularis mucosae (MM). One case of diagnosed MM had lymphoid invasion and lymph node metastasis to the upper mediastinum. After 1 year, although adjuvant treatment had been administered, there was lymph node recurrence in the left upper clavicle, and thus chemoradiation therapy was performed. Two other cases survived without recurrence. Early-stage EC is characterized by polypoid lesions with a slightly depressed lesion, and it is challenging to predict the histology on biopsy. Furthermore, it is difficult to determine the depth of invasion in the MM and submucosal layer in squamous cell carcinoma by endoscopy alone, and hence depth diagnosis by multiple modalities should be considered.
食管肉瘤样癌(EC)是一种罕见的恶性肿瘤,占食管癌的0.5 - 2.8%。大多数为进展期癌症,表现为息肉样病变,采用以手术为主的多学科治疗。然而,由于报道的早期EC病例极少,其内镜表现、病理表现及长期预后往往不明确。本文报告3例局限于黏膜层的EC。所有肿瘤的大体类型均为带有轻微凹陷病变的息肉样病变。所有病例在治疗前临床诊断为浸润性癌。肿瘤深度的病理诊断显示,1例侵犯黏膜固有层,2例侵犯黏膜肌层(MM)。1例诊断为MM的病例有淋巴浸润及上纵隔淋巴结转移。1年后,尽管给予了辅助治疗,但左锁骨上出现淋巴结复发,因此进行了放化疗。另外2例无复发存活。早期EC的特征为带有轻微凹陷病变的息肉样病变,活检时预测组织学表现具有挑战性。此外,仅通过内镜检查难以确定鳞状细胞癌在MM和黏膜下层的浸润深度,因此应考虑采用多种方式进行深度诊断。