Rovira J, Morales L, Parri F J, Juliá V, Claret I
Department of Pediatrics, Hospital Clinico Provincial, University of Barcelona, Spain.
J Pediatr Surg. 1989 Nov;24(11):1155-7. doi: 10.1016/s0022-3468(89)80103-4.
In this article two cases of idiopathic duodenal dilation are described. These cases meet the present criteria for segmental dilations of the intestine. The onset of the clinical features was acute in one case and chronic in the other. However, the radiological images were similar in both cases and provided the diagnosis. Surgical treatment consisted of duodenal resection and tapering and was curative in one case. The other patient died shortly after surgery. The duodenal specimens showed normal three-layer duodenal architecture in the pathology study. The intramural nervous plexi were unimpaired. Angiodysplasia was found in one case. Vascular abnormalities were also found in 10 other segmentary intestinal dilatations reported in the literature. The surgical implications of this new localization of segmentary intestinal dilatation are analyzed.
本文描述了两例特发性十二指肠扩张病例。这些病例符合目前肠道节段性扩张的标准。其中一例临床特征起病急性,另一例为慢性。然而,两例的放射影像相似,从而做出了诊断。手术治疗包括十二指肠切除和肠管缩窄,其中一例治愈。另一例患者术后不久死亡。病理研究显示十二指肠标本的十二指肠结构正常,分为三层。壁内神经丛未受损。其中一例发现血管发育异常。在文献报道的其他10例节段性肠扩张中也发现了血管异常。本文分析了这种节段性肠扩张新定位的手术意义。