Suzuki Toshiaki, Okamoto Tomoyoshi, Hanyu Ken, Suwa Katsuhito, Ashizuka Shuichi, Yanaga Katsuhiko
Department of Surgery, The Jikei Universiy, Daisan Hospital, Japan.
Department of Surgery, The Jikei Universiy, Daisan Hospital, Japan.
Int J Surg Case Rep. 2014;5(2):82-5. doi: 10.1016/j.ijscr.2013.12.018. Epub 2013 Dec 25.
Bochdalek's diaphragmatic hernia (BDH) rarely developed symptomatic in adulthood but mostly required an operation. In adult BDH cases, long-term residing of the massive intraabdominal organs in the thoracic cavity passively causes loss of domain for abdominal organs (LOD).
A 63-year-old man presented at our institution complaining of sudden left upper quadrant abdominal pain. Chest radiography showed a hyperdense lesion containing bowel gas in the left pleural space. Computed tomography revealed a dilated bowel above the diaphragm and intestinal obstruction suggestive of gangrenous changes. These findings were consistent with the diagnosis of incarcerated BDH and an emergency laparotomy was performed. Operative findings revealed the hypoplastic lung, lack of hernia sac, and location of the diaphragmatic defect, which indicated that his hernia was true congenital. Organs were reduced into the abdominal cavity, and large defect of the diaphragm was repaired with combination of direct vascular closure and intraperitoneal onlay mesh reinforcement using with expanded polytetrafluoroethylene (ePTFE) mesh. On the postoperative day 1, the patient fell into the shock and was diagnosed to have abdominal compartment syndrome (ACS). Conservative therapies were administered, but resulted in gastropleural fistula and pleural empyema, which required an emergency surgery. Mesh extraction and fistulectomy were performed.
A PubMed search for the case of ACS after repair of the adult BDH revealed only three cases, making this very rare condition.
In dealing with adult BDH, possible post-repair ACS should be considered.
博赫dalek氏膈肌疝(BDH)在成年期很少出现症状,但大多需要手术治疗。在成年BDH病例中,大量腹腔脏器长期位于胸腔会被动导致腹腔脏器失去空间(LOD)。
一名63岁男性因突发左上腹疼痛就诊于我院。胸部X线检查显示左胸腔内有一个含肠气的高密度病变。计算机断层扫描显示膈肌上方肠管扩张及肠梗阻,提示有坏疽性改变。这些发现与绞窄性BDH的诊断相符,遂行急诊剖腹手术。手术发现肺发育不全、无疝囊及膈肌缺损位置,表明其疝为真正的先天性。将脏器还纳腹腔,用直接血管闭合联合使用膨体聚四氟乙烯(ePTFE)补片的腹膜内覆盖补片加强术修复膈肌大缺损。术后第1天,患者陷入休克,被诊断为腹腔间隔室综合征(ACS)。给予保守治疗,但导致胃胸膜瘘和胸膜脓胸,这需要急诊手术。进行了补片取出和瘘管切除术。
对成年BDH修复术后发生ACS的病例进行PubMed检索仅发现3例,这是一种非常罕见的情况。
在处理成年BDH时,应考虑修复后可能发生的ACS。