-transparent.png){kind=logo}
Congenital pyloric atresia, a rare malformation producing gastric outlet obstruction during the neonatal period, was found in three patients. Sixty per cent of these malformations are membranous in type. Excision of the membrane and Heineke-Mikulicz pyloroplasty, which has been advocated as the procedure of choice, inevitably results in postoperative duodenogastric bile reflux. We suggest that to minimize reflux and hence possible increased risk of future development of gastric ulcer, maximal preservation of pyloric function in the operative management of the malformations is important.
Related Publications
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
October 1978,
Journal de radiologie, d'electrologie, et de medecine nucleaire,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
January 2005,
Annals of Saudi medicine,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
September 1979,
The Japanese journal of surgery,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
January 1971,
Surgery,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
July 2014,
Journal of pediatric surgery,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
January 2000,
Pediatric surgery international,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
October 2014,
Archivos argentinos de pediatria,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
January 2021,
Surgical case reports,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
April 1976,
Journal of pediatric surgery,
H Kadowaki, and
S Takeuchi, and
M Nakahira, and
C Yamada, and
S Tamate, and
C Shiokawa
May 1965,
Il Lattante,
