Papaziogas Basilios, Lazaridis Charalambos, Souparis Anastasios, Koutelidakis Ioannis, Grigoriou Marios, Dragoumis Dimitris, Atmatzidis Konstantinos
2nd Surgical Clinic, Aristotle University Hospital G. Gennimatas, Thessaloniki, Greece.
Med Princ Pract. 2007;16(2):151-4. doi: 10.1159/000098370.
We report a case of primary hypertrophic pyloric stenosis combined with a paraduodenal hernia in a 35-year-old woman.
The patient presented with signs of obstructive ileus. CT of the abdomen revealed a marked dilatation of the stomach and the proximal jejunum as well as a circumferential thickening of the antral-pyloric region with characteristics indicating hypertrophic pyloric stenosis. Exploratory laparotomy revealed the presence of a paraduodenal hernia containing jejunal loops and marked thickening of the pyloric region. The jejunum was reduced to its normal place and the ostium of the paraduodenal hernia closed with a running suture. The hypertrophic pyloric stenosis was treated with pyloromyotomy. Since the patient had no predisposing factors for the development of secondary pyloric stenosis, we considered the pyloric stenosis as congenital in origin.
To our knowledge this is the first reported case of congenital pyloric stenosis combined with the presence of a paraduodenal hernia in an adult.
我们报告一例35岁女性原发性肥厚性幽门狭窄合并十二指肠旁疝的病例。
患者表现为肠梗阻体征。腹部CT显示胃和空肠近端明显扩张,以及胃窦-幽门区域环形增厚,具有肥厚性幽门狭窄的特征。剖腹探查发现存在一个包含空肠袢的十二指肠旁疝,幽门区域明显增厚。将空肠复位至正常位置,用连续缝合法关闭十二指肠旁疝的开口。肥厚性幽门狭窄采用幽门肌切开术治疗。由于患者没有继发性幽门狭窄发生的易感因素,我们认为该幽门狭窄为先天性起源。
据我们所知,这是首例报道的成人先天性幽门狭窄合并十二指肠旁疝的病例。