G. Morrisstiff et al., LONG-TERM RESULTS OF SURGERY FOR CHILDHOOD ACHALASIA, Annals of the Royal College of Surgeons of England, 79(6), 1997, pp. 432-434
Childhood achalasia is an uncommon condition characterised by the abse
nce of oesophageal peristalsis together with increased resting pressur
e and failure of relaxation of the lower oesophageal sphincter. The cu
rrently accepted management is a modified Heller's cardiomyotomy with
Nissen fundoplication; however, the long-term results are uncertain. A
retrospective review of the notes of 10 children undergoing surgical
treatment of achalasia at our institution over a 23-year period were r
eviewed. There were six boys and four girls. The median age at onset o
f symptoms was 123 months and at diagnosis was 133 months. Five childr
en were below average weight at the time of presentation. All underwen
t a modified Heller's operation and Nissen fundoplication. The follow-
up ranged from 12 to 277 months with a mean of nearly 10 years. The re
sults were excellent in terms of symptomatic improvement in eight of t
en with one good and one moderate outcome. All children below average
weight have shown improvement postoperatively. We would conclude that
the management of achalasia in childhood should consist of an extended
Heller's cardiomyotomy performed by the abdominal approach with the a
ddition of an antireflux procedure such as Nissen fundoplication.