Endoscopic Balloon Dilation for Treatment of Congenital Antral Web / 대한소아소화기영양학회지
Pediatric Gastroenterology, Hepatology & Nutrition
; : 351-354, 2018.
Article
de En
| WPRIM
| ID: wpr-717799
Bibliothèque responsable:
WPRO
ABSTRACT
Congenital antral webs are a rare but relevant cause of gastric outlet obstruction in infants and children. The condition may lead to feeding refusal, vomiting, and poor growth. Due to the relative rarity of the disease, cases of congenital antral web are frequently misdiagnosed or diagnosed with significant delay as physicians favorably pursue diagnoses of pyloric stenosis and gastric ulcer disease, which are more prevalent. We report a case of an eight-month-old female who presented with persistent non-bilious emesis, feeding difficulties, and failure to thrive and was discovered to have an antral web. The web was successfully treated with endoscopic balloon dilation, which resolved her symptoms. Two years later, the patient remains asymptomatic and is thriving with weight at the 75th percentile for her age.
Mots clés
Texte intégral:
1
Indice:
WPRIM
Sujet Principal:
Pédiatrie
/
Sténose du pylore
/
Ulcère gastrique
/
Vomissement
/
Sténose du défilé gastrique
/
Diagnostic
/
Endoscopie
/
Retard de croissance staturo-pondérale
Type d'étude:
Diagnostic_studies
Limites du sujet:
Child
/
Female
/
Humans
/
Infant
langue:
En
Texte intégral:
Pediatric Gastroenterology, Hepatology & Nutrition
Année:
2018
Type:
Article