Taketo Ryoma, Ogawa Katsuhiro, Shibata Tomotaka, Fujinaga Atsuro, Akagi Tomonori, Ninomiya Shigeo, Ueda Yoshitake, Shiroshita Hidefumi, Etoh Tsuyoshi, Inomata Masafumi
Department of Gastroenterological and Pediatric Surgery, Faculty of Medicine, Oita University, Idaigaoka 1-1, Hasama-Machi, Oita, 879-5593, Japan.
Department of Comprehensive Surgery for Community Medicine, Faculty of Medicine, Oita University, Oita, Japan.
Clin J Gastroenterol. 2025 Feb;18(1):37-42. doi: 10.1007/s12328-024-02056-0. Epub 2024 Oct 30.
Epiphrenic esophageal diverticulum is rare and often associated with abnormalities of esophageal motility. Here, we report a case of a patient diagnosed with high-resolution manometry as having epiphrenic esophageal diverticulum with esophagogastric junction outflow obstruction, which were successfully treated with laparoscopic transhiatal surgery. A 59-year-old woman presented to our hospital for treatment of a symptomatic epiphrenic esophageal diverticulum. An esophagogram revealed a left epiphrenic diverticulum measuring 50 mm. High-resolution manometry showed a high integrated relaxation pressure of 35.6 mmHg (> 26 mmHg) and preserved esophageal peristalsis. A chest computed tomography scan showed no external compression of the distal esophagus. Therefore, we diagnosed an epiphrenic esophageal diverticulum with esophagogastric junction outflow obstruction according to the Chicago Classification v3.0. Laparoscopic transhiatal diverticulectomy, planned and selective myotomy, and Dor fundoplication were performed. We performed myotomy just on the esophageal side and did not perform gastric myotomy. The postoperative course was uneventful, and the postoperative esophagogram showed smooth passage of contrast without leakage or stenosis. High-resolution manometry showed a normal integrated relaxation pressure (11.6 mmHg) at three months after surgery. Because an epiphrenic esophageal diverticulum is frequently associated with esophageal motility disorder, not only morphologic but also functional and appropriate treatment must be considered.
膈上型食管憩室较为罕见,常与食管动力异常相关。在此,我们报告一例患者,经高分辨率测压诊断为膈上型食管憩室合并食管胃交界部流出道梗阻,通过腹腔镜经裂孔手术成功治愈。一名59岁女性因有症状的膈上型食管憩室前来我院就诊。食管造影显示一个50毫米的左侧膈上型憩室。高分辨率测压显示综合松弛压较高,为35.6毫米汞柱(>26毫米汞柱),且食管蠕动保留。胸部计算机断层扫描显示食管远端无外部压迫。因此,根据芝加哥分类v3.0,我们诊断为膈上型食管憩室合并食管胃交界部流出道梗阻。实施了腹腔镜经裂孔憩室切除术、计划性选择性肌切开术和Dor胃底折叠术。我们仅在食管侧进行肌切开术,未进行胃肌切开术。术后过程顺利,术后食管造影显示造影剂通过顺畅,无渗漏或狭窄。术后三个月高分辨率测压显示综合松弛压正常(11.6毫米汞柱)。由于膈上型食管憩室常与食管动力障碍相关,不仅要考虑形态学治疗,还必须考虑功能性和适当的治疗。