Higa S, Matsumoto M, Tamai O, Yamada M, Kusano T, Muto Y, Kiyuna M, Toda T
First Department of Surgery, Ryukyu University School of Medicine, Okinawa, Japan.
J Gastroenterol. 1996 Feb;31(1):100-4. doi: 10.1007/BF01211194.
A plexiform variant of leiomyoma of the esophagus in a 51-year-old woman is reported. The patient was diagnosed with a tumor of the esophagus in an X-ray mass survey of the upper gastrointestinal tract. She was referred to the Ryukyu University Hospital for further examination. She appeared healthy with no complaints. Upper gastrointestinal series revealed an oval, well-defined filling defect in the lower esophagus just above the esophagogastric junction. Endoscopy revealed an undulating bulge covered with normal esophageal mucosa. Endoscopic ultrasonography showed a sharply demarcated hypoechoic mural tumor with internal linear pattern, with no evidence of penetration into the surrounding tissue. These findings were evaluated as consistent with a leiomyoma. Removing the tumor by enucleation was easily accomplished. Unexpectedly, on gross inspection, the tumor was a plexiform type, mimicking a plexiform neurofibroma. Light and electron microscopic examination and immunohistochemistry of the tumor tissue confirmed leiomyoma. Since the enucleation of the tumor, the patient has been free of recurrence and symptoms for 1.5 years at the time of this report.
报告了一名51岁女性食管平滑肌瘤的丛状变型。该患者在上消化道X线肿块检查中被诊断为食管肿瘤。她被转诊至琉球大学医院进行进一步检查。她看起来健康,无任何不适主诉。上消化道造影显示在食管胃交界处上方的下段食管有一个椭圆形、边界清晰的充盈缺损。内镜检查显示一个起伏的隆起,表面覆盖正常食管黏膜。内镜超声显示一个边界清晰的低回声壁层肿瘤,内部呈线性结构,无周围组织浸润迹象。这些表现被评估为与平滑肌瘤一致。通过摘除术轻松切除了肿瘤。出乎意料的是,大体检查时肿瘤为丛状型,类似丛状神经纤维瘤。对肿瘤组织进行光镜和电镜检查及免疫组化证实为平滑肌瘤。自肿瘤摘除以来,至本报告时患者已无复发且无症状达1.5年。