Singh H, Gupta H L, Sethi R S, Khetarpal S K
Postgrad Med J. 1969 May;45(523):327-35. doi: 10.1136/pgmj.45.523.327.
Cardiac achalasia is a disorder not unknown in the paediatric age-group and may occur even in the neonatal period. This disorder should, therefore, be considered in all cases presenting with persistent vomiting, as well as in those with chronic respiratory disease in whom more common causes have been excluded. It is almost universally accepted that the disorder results from a disturbed function of ganglion cells in the distal oesophagus, as the disease has been reproduced in laboratory animals by denervation of the distal oesophagus. The exact pathogenesis of this degenerative change is not well understood. However, in at least some of the cases congenital absence of the ganglion cells may be responsible for this functional disturbance. This is inferred from the fact that the disease may be found in association with Hirschsprung disease, in which there is a congenital absence of ganglion cells in the terminal colon. Moreover, the occurrence of the disease in the neonatal period itself favours a congenital lesion. Surgery was preferred to other forms of treatment in the paediatric age-group in view of the reported equivocal response to mechanical dilatation and pre-disposition of children to respiratory complications. The results of surgery were satisfactory.
贲门失弛缓症在儿童年龄组中并非罕见,甚至在新生儿期也可能发生。因此,对于所有出现持续性呕吐的病例,以及排除了更常见病因的慢性呼吸道疾病病例,都应考虑这种疾病。几乎普遍认为,这种疾病是由远端食管神经节细胞功能紊乱引起的,因为通过对远端食管进行去神经支配,这种疾病已在实验动物中重现。这种退行性变化的确切发病机制尚不完全清楚。然而,至少在某些病例中,神经节细胞的先天性缺失可能是这种功能障碍的原因。这是从以下事实推断出来的:这种疾病可能与先天性巨结肠病有关,在先天性巨结肠病中,末端结肠存在神经节细胞的先天性缺失。此外,该疾病在新生儿期本身的发生也支持先天性病变。鉴于报道的对机械扩张的反应不明确以及儿童易发生呼吸并发症,在儿童年龄组中,手术比其他治疗形式更受青睐。手术结果令人满意。