Aiko S, Yoshizumi Y, Sugiura Y, Koike H, Marui T, Aida S, Sato K, Tanaka S
Department of Surgery II, National Defense Medical College, Saitama, Japan.
Dis Esophagus. 1998 Oct;11(4):263-7. doi: 10.1093/dote/11.4.263.
We report a case of esophageal leiomyosarcoma that possibly arose from the muscularis mucosae, thereby showing a particularly unusual appearance. A large polypoid intraluminal lesion in the distal esophagus was found on an endoscopic examination of a 68-year-old man with a 3-month history of dysphagia. Although the histological examination of biopsy specimens clearly revealed leiomyosarcoma, the absence of an exophytic component on computed tomography (CT) scan caused us to suspect that the tumor was carcinosarcoma. The tumor was resected by a subtotal esophagectomy. Microscopic evaluation revealed no involvement in the layer of the muscularis propria and no component of carcinoma. Clinical features of the pedunculated esophageal leiomyosarcoma shown in this case and three additional cases previously reported in the literature are reviewed.
我们报告一例可能起源于黏膜肌层的食管平滑肌肉瘤,其表现极为罕见。一名68岁男性,有3个月吞咽困难病史,内镜检查发现食管远端有一个大的息肉样腔内病变。尽管活检标本的组织学检查明确显示为平滑肌肉瘤,但计算机断层扫描(CT)未发现外生性成分,这使我们怀疑该肿瘤为癌肉瘤。该肿瘤通过食管次全切除术切除。显微镜评估显示肿瘤未累及固有肌层,也无癌成分。本文回顾了该病例以及先前文献报道的另外3例带蒂食管平滑肌肉瘤的临床特征。