Cardiac achalasia in childhood

• Published in: Postgraduate medical journal 1969-05, Vol.45 (523), p.327-335
• Main Authors: Singh, Harjit, Sethi, R. S., Gupta, H. L., Khetarpal, S. K.
• Format: Article
• Language: English
• Subjects: Child; Clinical Review; Dilatation; Esophageal Achalasia - diagnostic imaging; Esophageal Achalasia - surgery; Female; Humans; Infant; Male; Radiography
• ISSN: 0032-5473; 1469-0756
• 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.