Tatagari Vishwant, Devine Adam, Cronin Brian, Vaughn David
Department of Anesthesia, UPMC Lititz, 1500 Highlands Drive, Lititz, PA 17543, USA.
Department of Internal Medicine, UPMC Lititz, 1500 Highlands Drive, Lititz, PA 17543, USA.
Int J Surg Case Rep. 2022 May;94:107015. doi: 10.1016/j.ijscr.2022.107015. Epub 2022 Apr 3.
Herniation through the Foramen of Winslow, also known as the epiploic foramen, is an extremely rare phenomenon with less than 200 cases reported in medical literature. Internal hernias account for less than 1% of all hernias and roughly 8% of all internal hernias occur through the foramen of Winslow. We present a case of a foramen of Winslow hernia that was not detected until direct visualization with laparoscopy.
A 52 year-old healthy female with a surgical history of a Caesarean section presented to the ER with severe epigastric pain radiating to her back. Physical exam was positive for abdominal tenderness and guarding. Vital signs were within normal limits. Murphy's sign and Rovsing's sign were negative. Initial imaging studies, including a CT scan of the abdomen, and laboratory findings were unremarkable. A hepatobiliary iminodiacetic acid (HIDA) scan was performed and demonstrated non-visualization of the gallbladder suggestive of acute vs. chronic cholecystitis. Following these results the patient elected to undergo exploratory laparoscopy with potential cholecystectomy. Intra-operatively, the colon was noted to be herniated through the foramen of Winslow. The procedure was converted to an open laparotomy. The hernia was manually reduced, and a right hemicolectomy was performed to prevent recurrence of the hernia.
Reports list an enlarged foramen of Winslow, excessive viscera mobility (i.e., persistent ascending mesocolon or long small bowel mesentery), and an increase in intra-abdominal pressure as potential risk factors for this particular hernia. In our case, the patient was noted to have excessive mobility of the viscera with the presence of persistent ascending mesocolon and an abnormally long right mesentery. Physical exam is usually nonspecific and laboratory findings are typically unremarkable, posing a diagnostic challenge. Additionally, radiological findings indicating presence of an internal hernia were missed in the initial CT scan read by the radiologist. Internal hernias need to be managed surgically as there is a risk of strangulation with bowel ischemia.
This rare radiographic phenomenon is difficult to diagnose radiographically and warrants further workup due to the potential risk of bowel strangulation despite negative clinical and laboratory findings.
经网膜孔疝出,也称为网膜孔疝,是一种极为罕见的现象,医学文献报道的病例不足200例。内疝占所有疝的比例不到1%,而所有内疝中约8%是通过网膜孔发生的。我们报告一例网膜孔疝,直到通过腹腔镜直接观察才被发现。
一名52岁健康女性,有剖宫产手术史,因严重上腹部疼痛放射至背部就诊于急诊科。体格检查发现腹部压痛和肌紧张阳性。生命体征在正常范围内。墨菲氏征和罗夫辛氏征阴性。包括腹部CT扫描在内的初始影像学检查以及实验室检查结果均无异常。进行了肝胆亚氨基二乙酸(HIDA)扫描,结果显示胆囊不显影,提示急性或慢性胆囊炎。基于这些结果,患者选择接受可能行胆囊切除术的 exploratory laparoscopy。术中发现结肠经网膜孔疝出。手术改为开腹手术。手动还纳疝内容物,并进行了右半结肠切除术以防止疝复发。
报告列出网膜孔扩大、内脏活动度增加(即持续上升的结肠系膜或长的小肠系膜)以及腹内压升高是这种特殊疝的潜在危险因素。在我们的病例中,发现患者存在持续上升的结肠系膜和异常长的右系膜,导致内脏活动度增加。体格检查通常无特异性,实验室检查结果通常也无异常,这给诊断带来了挑战。此外,放射科医生在初始CT扫描解读中遗漏了提示内疝存在的影像学表现。由于存在肠绞窄和肠缺血的风险,内疝需要手术治疗。
这种罕见的影像学现象在影像学上难以诊断,尽管临床和实验室检查结果为阴性,但由于存在肠绞窄的潜在风险,仍需要进一步检查。