Histological inflammatory changes after surgery at the epithelium of the distal esophagus in patients with Barrett's esophagus: a comparison of two surgical procedures

被引:8
作者
Braghetto, I
Csendes, A
Smok, G
Gradiz, M
Mariani, V
Compan, A
Guerra, JF
Burdiles, P
Korn, O
机构
[1] Clin Hosp Univ Chile, Dept Surg, Santiago, Chile
[2] Clin Hosp Univ Chile, Dept Pathol, Santiago, Chile
关键词
antireflux surgery; Barrett's mucosa; inflammation;
D O I
10.1111/j.1442-2050.2004.00414.x
中图分类号
R57 [消化系及腹部疾病];
学科分类号
摘要
There are many reports concerning the surgical treatment of patients with Barrett's esophagus, but very few focus on histological changes of inflammatory cells in squamous and columnar epithelium before and late after classic antireflux or acid suppression-duodenal diversion surgery. We evaluate the impact of these procedures in the presence of intestinal metaplasia, dysplasia and Helicobacter pylori in the columnar epithelium. Two groups of patients were studied, 37 subjected to classic antireflux and 96 to acid suppression-duodenal diversion operations. They were subjected to endoscopic and histological studies before and at 1, 3 and more than 5 years after surgery. Manometric evaluations and 24 h pH monitoring were performed before and at 1 year after surgery. The presence of inflammatory cells at both the squamous and columnar epithelium was significantly higher at the late follow up in patients subjected to classic antireflux surgery compared with patients subjected to acid suppression-duodenal diversion operations (P < 0.02 and P < 0.001, respectively). Intestinal metaplasia, present in 100% of patients before surgery, had decreased significantly at 3 years after surgery in patients subjected to acid suppression-duodenal diversion operations compared with classic antireflux procedures, 75% versus 53%, respectively (P < 0.001). The presence of Helicobacter pylori did not vary before or after surgery in either group. In conclusion, acid suppression-duodenal diversion operations are followed by a decreased presence of inflammatory cells in both squamous and columnar epithelium compared with classic antireflux surgery in patients with Barrett's esophagus. Intestinal metaplasia and dysplasia and inflammation findings were also less common after acid suppression-duodenal diversion operation.
引用
收藏
页码:235 / 242
页数:8
相关论文
共 67 条
  • [41] Barrett's esophagus: Does an antireflux procedure reduce the need for endoscopic surveillance?
    McDonald, ML
    Trastek, VF
    Allen, MS
    Deschamps, C
    Pairolero, PC
    [J]. JOURNAL OF THORACIC AND CARDIOVASCULAR SURGERY, 1996, 111 (06) : 1135 - 1139
  • [42] MCENTEE GP, 1991, GULLET, V1, P169
  • [43] Inflammation and specialized intestinal metaplasia of cardiac mucosa is a manifestation of gastroesophageal reflux disease
    Oberg, S
    Peters, JH
    DeMeester, TR
    Chandrasoma, P
    Hagen, JA
    Ireland, AP
    Ritter, MP
    Mason, RJ
    Crookes, P
    Bremner, CG
    [J]. ANNALS OF SURGERY, 1997, 226 (04) : 522 - 530
  • [44] Endoscopic surveillance of columnar-lined esophagus -: Frequency of intestinal metaplasia detection and impact of antireflux surgery
    Öberg, S
    Johansson, J
    Wenner, J
    Johnsson, F
    Zilling, T
    von Holstein, CS
    Nilsson, J
    Walther, B
    [J]. ANNALS OF SURGERY, 2001, 234 (05) : 619 - 626
  • [45] Ortiz A, 1996, BRIT J SURG, V83, P274
  • [46] INCREASING INCIDENCE OF ADENOCARCINOMA OF THE ESOPHAGUS AND ESOPHAGOGASTRIC JUNCTION
    PERA, M
    CAMERON, AJ
    TRASTEK, VF
    CARPENTER, HA
    ZINSMEISTER, AR
    [J]. GASTROENTEROLOGY, 1993, 104 (02) : 510 - 513
  • [47] Endoscopic regression of Barrett's oesophagus during omeprazole treatment; a randomised double blind study
    Peters, FTM
    Ganesh, S
    Kuipers, EJ
    Sluiter, WJ
    Klinkenberg-Knol, EC
    Lamers, CBHW
    Kleibeuker, JH
    [J]. GUT, 1999, 45 (04) : 489 - 494
  • [48] Peters FTM, 2000, SCAND J GASTROENTERO, V35, P1238
  • [49] Barrett's esophagus: Now what?
    Peters, JH
    [J]. ANNALS OF SURGERY, 2003, 237 (03) : 299 - 300
  • [50] Riddell RH, 1996, AM J SURG PATHOL, V20, pS31