Congenital hypertrophic pyloric stenosis (Q46319): Difference between revisions

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Malformação congênita não incomum do estômago de causa desconhecida, na qual há hipertrofia e hiperplasia do músculo circular do piloro. Sintomas de obstrução de via de saída gástrica geralmente aparecem entre a terceira e a sexta semanas de vida. A anomalia se manifesta por vômitos intermitentes (que aumentam de frequência e se transformam em vômitos em jato), regurgitação, perda de peso, desidratação, desequilíbrio eletrolítico, às vezes uma pequena massa pilórica palpável e contrações peristálticas visíveis no epigástrio; também pode haver icterícia. Alguns casos parecem ter origem familial (possivelmente de herança autossômica dominante).
description / endescription / en
 
A not uncommon congenital malformation of the stomach of unknown cause in which there is hypertrophy and hyperplasia of the circular muscle of the pylorus. Symptoms of gastric outlet obstruction usually appear between the third and sixth weeks of life. The anomaly is manifested by intermittent vomiting (which increases in frequency and becomes projectile), regurgitation, weight loss, dehydration, electrolyte imbalance, sometimes a small palpable pyloric mass, and visible peristaltic contractions across the epigastrium; there may also be jaundice. Some cases appear to be familial (possibly of autosomal dominant inheritance).
Property / Canonical URI
 
Property / Canonical URI: https://id.who.int/icd/entity/224753192 / rank
 
Normal rank
Property / CURIE
 
CID11:LB13.0
Property / CURIE: CID11:LB13.0 / rank
 
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Property / Canary Token
 
dki-india-LB13.0
Property / Canary Token: dki-india-LB13.0 / rank
 
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Property / Verification Status
 
Concluído
Property / Verification Status: Concluído / rank
 
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Property / Knowledge Architect
 
Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank
 
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Property / Collection date
 
13 August 2026
Timestamp+2026-08-13T00:00:00Z
Timezone+00:00
CalendarGregorian
Precision1 day
Before0
After0
Property / Collection date: 13 August 2026 / rank
 
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Property / Linked ICD 10
 
Property / Linked ICD 10: Q40.0 / rank
 
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Latest revision as of 14:49, 13 August 2026

A not uncommon congenital malformation of the stomach of unknown cause in which there is hypertrophy and hyperplasia of the circular muscle of the pylorus. Symptoms of gastric outlet obstruction usually appear between the third and sixth weeks of life. The anomaly is manifested by intermittent vomiting (which increases in frequency and becomes projectile), regurgitation, weight loss, dehydration, electrolyte imbalance, sometimes a small palpable pyloric mass, and visible peristaltic contractions across the epigastrium; there may also be jaundice. Some cases appear to be familial (possibly of autosomal dominant inheritance).
Language Label Description Also known as
default for all languages
LB13.0
    English
    Congenital hypertrophic pyloric stenosis
    A not uncommon congenital malformation of the stomach of unknown cause in which there is hypertrophy and hyperplasia of the circular muscle of the pylorus. Symptoms of gastric outlet obstruction usually appear between the third and sixth weeks of life. The anomaly is manifested by intermittent vomiting (which increases in frequency and becomes projectile), regurgitation, weight loss, dehydration, electrolyte imbalance, sometimes a small palpable pyloric mass, and visible peristaltic contractions across the epigastrium; there may also be jaundice. Some cases appear to be familial (possibly of autosomal dominant inheritance).

      Statements

      CID11:LB13.0
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      dki-india-LB13.0
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      Concluído
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      13 August 2026
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