Development of infantile hypertrophic pyloric stenosis in patients treated for oesophageal atresia. A case report

N Qvist, L Rasmussen, L P Hansen, S A Pedersen

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

Resumé

Two cases of infantile hypertrophic pyloric stenosis (IHPS) developed in 74 patients treated for oesophageal atresia. Treatment of oesophageal atresia is frequently followed by vomiting and failure to thrive due to gastrooesophageal reflux or anastomotic stricture. The diagnose of IHPS must be considered in such patients under the age of 8 weeks as symptoms of IHPS are similar to those of gastrooesophageal reflux. The diagnose of IHPS is strongly supported by the presence of a non-carbonic alkalosis. Contrast studies including oesophagus, stomach and duodenum are to be made early in the course, as clinical signs of IHPS are often masked
OriginalsprogEngelsk
TidsskriftActa Chirurgica Scandinavica
Vol/bind152
Sider (fra-til)237-8
Antal sider2
ISSN0001-5482
StatusUdgivet - mar. 1986

Fingeraftryk

Esophageal Atresia
Gastroesophageal Reflux
Failure to Thrive
Alkalosis
Duodenum
Esophagus
Pathologic Constriction
Infantile Hypertrophic 1 Pyloric Stenosis

Emneord

  • Esophageal Atresia
  • Humans
  • Hypertrophy
  • Infant, Newborn
  • Male
  • Postoperative Complications
  • Pyloric Stenosis

Citer dette

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abstract = "Two cases of infantile hypertrophic pyloric stenosis (IHPS) developed in 74 patients treated for oesophageal atresia. Treatment of oesophageal atresia is frequently followed by vomiting and failure to thrive due to gastrooesophageal reflux or anastomotic stricture. The diagnose of IHPS must be considered in such patients under the age of 8 weeks as symptoms of IHPS are similar to those of gastrooesophageal reflux. The diagnose of IHPS is strongly supported by the presence of a non-carbonic alkalosis. Contrast studies including oesophagus, stomach and duodenum are to be made early in the course, as clinical signs of IHPS are often masked.",
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Development of infantile hypertrophic pyloric stenosis in patients treated for oesophageal atresia. A case report. / Qvist, N; Rasmussen, L; Hansen, L P; Pedersen, S A.

I: Acta Chirurgica Scandinavica, Bind 152, 03.1986, s. 237-8.

Publikation: Bidrag til tidsskriftTidsskriftartikelForskningpeer review

TY - JOUR

T1 - Development of infantile hypertrophic pyloric stenosis in patients treated for oesophageal atresia. A case report

AU - Qvist, N

AU - Rasmussen, L

AU - Hansen, L P

AU - Pedersen, S A

PY - 1986/3

Y1 - 1986/3

N2 - Two cases of infantile hypertrophic pyloric stenosis (IHPS) developed in 74 patients treated for oesophageal atresia. Treatment of oesophageal atresia is frequently followed by vomiting and failure to thrive due to gastrooesophageal reflux or anastomotic stricture. The diagnose of IHPS must be considered in such patients under the age of 8 weeks as symptoms of IHPS are similar to those of gastrooesophageal reflux. The diagnose of IHPS is strongly supported by the presence of a non-carbonic alkalosis. Contrast studies including oesophagus, stomach and duodenum are to be made early in the course, as clinical signs of IHPS are often masked.

AB - Two cases of infantile hypertrophic pyloric stenosis (IHPS) developed in 74 patients treated for oesophageal atresia. Treatment of oesophageal atresia is frequently followed by vomiting and failure to thrive due to gastrooesophageal reflux or anastomotic stricture. The diagnose of IHPS must be considered in such patients under the age of 8 weeks as symptoms of IHPS are similar to those of gastrooesophageal reflux. The diagnose of IHPS is strongly supported by the presence of a non-carbonic alkalosis. Contrast studies including oesophagus, stomach and duodenum are to be made early in the course, as clinical signs of IHPS are often masked.

KW - Esophageal Atresia

KW - Humans

KW - Hypertrophy

KW - Infant, Newborn

KW - Male

KW - Postoperative Complications

KW - Pyloric Stenosis

M3 - Journal article

C2 - 3716746

VL - 152

SP - 237

EP - 238

JO - B J U International (Print)

JF - B J U International (Print)

SN - 1464-4096

ER -