Interstitial cells of Cajal are decreased in patients with gastroschisis associated intestinal dysmotility

被引:18
|
作者
Zani-Ruttenstock, Elke [1 ]
Zani, Augusto [1 ]
Paul, Anu [1 ]
Diaz-Cano, Salvador [1 ]
Ade-Ajayi, Niyi [1 ]
机构
[1] Kings Coll Hosp London, Dept Paediat Surg, London SE5 9RS, England
关键词
Gastroschisis; Intestinal dysmotility; Cajal cells; Peristalsis; Outcome; ABDOMINAL-WALL DEFECTS; SMOOTH-MUSCLE-CELLS; FETAL LAMB MODEL; RAT MODEL; HIRSCHSPRUNG DISEASE; REPERFUSION INJURY; MYENTERIC PLEXUS; MANAGEMENT; EUROPE; HEALTH;
D O I
10.1016/j.jpedsurg.2015.02.029
中图分类号
R72 [儿科学];
学科分类号
100202 ;
摘要
Background: Gastroschisis associated intestinal dysmotility (GAID) is poorly understood. Animal experiments suggest that interstitial cells of Cajal (ICC), play an important role. Methods: Infants with gastroschisis (GS) and GAID (time to full feed >42 days) were selected. Age matched GS and control (NEC, ileal atresia, malrotation, and volvulus) samples from primary (T1) and secondary (T2) time points underwent standard histopathology and immunohistochemistry for identification of ICC, followed by evaluation of ICC numbers, distribution, morphology, relation to ganglion cells, and myenteric plexus architecture. Groups were compared using parametric and nonparametric tests. Main Results: Twelve patients had samples available for histopathological evaluation. GAID patients had a significantly lower total number of ICCs than controls (3 vs. 8, P < 0.0029). ICC number at T1 was 2.5 vs. 6 (P = 0.0629) and significantly lower at T2. (3.5 vs. 11, P = 0.0124). GAID patients did not show a significant increase of ICC from T1 to T2. Controls showed a significant increase of ICC over time (6 vs. 11, P = 0.0408). Conclusion: Intestinal samples from infants with GAID who underwent stoma formation demonstrated fewer ICC than controls. There was no improvement or cell recovery during the study period. The ability to modulate ICC may have significant implications for the management of GAID. (C) 2015 Published by Elsevier Inc.
引用
收藏
页码:750 / 754
页数:5
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