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Intestinal neuronal dysplasia-like histopathology in infancy.
Hirayama, Yutaka; Iinuma, Yasushi; Numano, Fujito; Masui, Daisuke; Iida, Hisataka; Komatsuzaki, Naoko; Nagayama, Yosihisa; Naito, Shinichi; Nitta, Koju.
Afiliación
  • Hirayama Y; Department of Pediatric Surgery, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Iinuma Y; Department of Pediatric Surgery, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Numano F; Department of Neonatology, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Masui D; Department of Pediatric Surgery, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Iida H; Department of Pediatric Surgery, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Komatsuzaki N; Department of Pediatric Surgery, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Nagayama Y; Department of Neonatology, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Naito S; Department of Pediatric Surgery, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
  • Nitta K; Department of Pediatric Surgery, Perinatal Medical Center, Niigata City General Hospital, Niigata, Japan.
Pediatr Int ; 57(3): 491-3, 2015 Jun.
Article en En | MEDLINE | ID: mdl-25711721
ABSTRACT
The present patient was delivered at a gestational age of 27 weeks. She had abdominal bloating with symptoms of respiratory distress. We suspected Hirschsprung disease (HD) or small intestinal stricture, but examinations were not definitive. Exploratory laparotomy was performed at 97 days of age. Intraoperative findings showed no evidence of small intestinal stricture or changes in intestinal caliber. A transanal drainage tube was inserted, and decompression therapy and intestinal lavage were started. Rectal mucosal biopsy was performed at 184 days of age, and HE and acetylcholinesterase staining showed intestinal neuronal dysplasia (IND)-like pathological findings. At 15 months, giant ganglia were no longer present on follow-up rectal mucosal biopsy, and the pathological diagnosis was normoganglionosis. It should be recognized that while the enteric nervous system is developing, IND-like pathological findings may be seen as a pathological condition during the maturation process.
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Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sistema Nervioso Entérico / Anomalías del Sistema Digestivo / Enfermedad de Hirschsprung / Mucosa Intestinal Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Infant Idioma: En Revista: Pediatr Int Asunto de la revista: PEDIATRIA Año: 2015 Tipo del documento: Article País de afiliación: Japón

Texto completo: 1 Bases de datos: MEDLINE Asunto principal: Sistema Nervioso Entérico / Anomalías del Sistema Digestivo / Enfermedad de Hirschsprung / Mucosa Intestinal Tipo de estudio: Diagnostic_studies Límite: Female / Humans / Infant Idioma: En Revista: Pediatr Int Asunto de la revista: PEDIATRIA Año: 2015 Tipo del documento: Article País de afiliación: Japón