Rao Min, Meng Qing-Qing, Gao Pu-Jun
Department of Hepatology and Gastroenterology, The Second Part of First Hospital of Jilin University, Changchun 130021, Jilin Province, China.
Department of Hepatology, The First Hospital of Jilin University, Changchun 130021, Jilin Province, China.
World J Clin Cases. 2020 Nov 26;8(22):5809-5815. doi: 10.12998/wjcc.v8.i22.5809.
Benign esophageal tumors are rare accounting for < 1% of esophageal tumors; two-thirds of which are leiomyomas. Esophageal leiomyoma is a benign tumor derived from mesenchymal tissue that is completely muscularly differentiated. Most esophageal leiomyomas are < 5 cm. Esophageal leiomyomas > 5 cm are rare. We describe a case of a large esophageal leiomyoma involving the cardia and diaphragm.
A 35-year-old woman presented to the doctor because of a choking sensation after eating. Physical examination showed no positive signs. Gastroscopy indicated an uplifted change in the cardia. Enhanced computed tomography revealed space-occupying lesions in the lower part of the esophagus and cardia, which were likely to be malignant. Positron emission tomography-computed tomography showed increased metabolism of soft tissue masses in the lower esophagus and near the cardia. Malignant lesions were considered, and mesenchymal tumors were not excluded. Endoscopic ultrasonography was performed to examine a hypoechoic mass in the lower esophagus, which was unclear from the esophageal wall. Clinical evaluation suggested diagnosis of esophageal and cardiac stromal tumors. Finally, histological specimens obtained by endoscopic ultrasonography- fine needle aspiration suggested leiomyoma. The patient underwent laparoscopic local resection of the tumor. The postoperative pathological diagnosis was leiomyoma.
Endoscopic ultrasonography-fine needle aspiration is necessary for the diagnosis of gastrointestinal leiomyomas. It provides a strong basis for diagnosis of gastrointestinal tumors of unknown nature and origin.
良性食管肿瘤较为罕见,占食管肿瘤的比例不到1%;其中三分之二为平滑肌瘤。食管平滑肌瘤是一种源自间叶组织的良性肿瘤,具有完全的肌肉分化。大多数食管平滑肌瘤直径小于5厘米。直径大于5厘米的食管平滑肌瘤较为罕见。我们报告一例累及贲门和膈肌的巨大食管平滑肌瘤病例。
一名35岁女性因进食后有哽噎感就诊。体格检查未发现阳性体征。胃镜检查显示贲门处有隆起改变。增强计算机断层扫描显示食管下段和贲门有占位性病变,可能为恶性。正电子发射断层扫描-计算机断层扫描显示食管下段和贲门附近软组织肿块代谢增加。考虑为恶性病变,不排除间叶组织肿瘤。进行了内镜超声检查,发现食管下段有一低回声肿块,与食管壁分界不清。临床评估提示诊断为食管和心脏间质瘤。最后,通过内镜超声引导下细针穿刺获取的组织学标本提示为平滑肌瘤。患者接受了腹腔镜下肿瘤局部切除术。术后病理诊断为平滑肌瘤。
内镜超声引导下细针穿刺对于胃肠道平滑肌瘤的诊断是必要的。它为诊断性质和起源不明的胃肠道肿瘤提供了有力依据。