Infant presenting with pyloric stenosis and autosomal recessive polycystic kidney disease at 36 weeks' postmenstrual age (PMA).
BMJ Case Rep
; 14(5)2021 May 19.
Article
en En
| MEDLINE
| ID: mdl-34011647
ABSTRACT
This case report describes a premature male infant born after a pregnancy complicated by oligohydramnios of unknown aetiology but otherwise unremarkable prenatal scans. He had sudden onset of projectile emesis and severe hypertension in the third week of life, and further investigations revealed both pyloric stenosis and polycystic kidneys, at just 36 weeks' postmenstrual age (PMA). His course thereafter was complicated by severe refractory hypertension requiring multiple antihypertensive agents in order to gain control, although his renal function remained normal. Few case reports have previously described this unusual association, but none have presented with both entities at such an early PMA.
Palabras clave
Texto completo:
1
Colección:
01-internacional
Banco de datos:
MEDLINE
Asunto principal:
Estenosis Pilórica
/
Oligohidramnios
/
Riñón Poliquístico Autosómico Recesivo
/
Enfermedades del Prematuro
Tipo de estudio:
Diagnostic_studies
Límite:
Female
/
Humans
/
Infant
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Male
/
Newborn
/
Pregnancy
Idioma:
En
Revista:
BMJ Case Rep
Año:
2021
Tipo del documento:
Article
País de afiliación:
Estados Unidos