Catalogo Articoli (Spogli Riviste)

OPAC HELP

Titolo:
Airway anomalies in patients with congenital diaphragmatic hernia
Autore:
Nose, K; Kamata, S; Sawai, T; Tazuke, Y; Usui, N; Kawahara, H; Okada, A;
Indirizzi:
Osaka Univ, Sch Med, Dept Pediat Surg, Suita, Osaka 5650871, Japan Osaka Univ Suita Osaka Japan 5650871 at Surg, Suita, Osaka 5650871, Japan
Titolo Testata:
JOURNAL OF PEDIATRIC SURGERY
fascicolo: 11, volume: 35, anno: 2000,
pagine: 1562 - 1565
SICI:
0022-3468(200011)35:11<1562:AAIPWC>2.0.ZU;2-M
Fonte:
ISI
Lingua:
ENG
Soggetto:
CYSTIC ADENOMATOID MALFORMATION; PULMONARY HYPOPLASIA; SEQUESTRATION; INFANTS;
Keywords:
congenital diaphragmatic hernia; anomalies of tracheobronchial tree; pulmonary hypoplasia; bronchoscopy;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
22
Recensione:
Indirizzi per estratti:
Indirizzo: Kamata, S Osaka Univ, Sch Med, Dept Pediat Surg, 2-2 Yamadaoka, Suita, Osaka 5650871, Japan Osaka Univ 2-2 Yamadaoka Suita Osaka Japan 5650871 650871, Japan
Citazione:
K. Nose et al., "Airway anomalies in patients with congenital diaphragmatic hernia", J PED SURG, 35(11), 2000, pp. 1562-1565

Abstract

Purpose: Congenital diaphragmatic hernias (CDH) sometimes are associated with airway anomalies such as congenital stenosis, abnormal branching of thebronchi, and pulmonary hypoplasia. The incidence of these associated airway anomalies has not been reported previously. Methods: Bronchoscopy was performed in all neonates with CDH from 1987 to 1999. In addition to anatomic anomalies, bronchial hypoplasia was defined as narrowing and shortening of the bronchi at bronchoscopy. Results: Anatomic anomalies were identified in 7 of 39 patients with CDH: 1 had congenital tracheal stenosis with pulmonary artery sling, 1 had a defect of the right upper robe bronchus, 2 had a tracheal bronchus, and 3 had a trifurcated trachea. Bronchial hypoplasia on the affected side was identified in 15 patients and was seen in all patients with anatomic anomalies ofthe tracheobronchial tree except the 2 with tracheal bronchus. After excluding 5 patients with severe associated anomalies, 6 of 14 patients with an abnormal tracheobronchial tree died, whereas 1 of 20 patients without airway abnormalities died. Conclusions: Anatomic anomalies of the tracheobronchial tree and bronchialhypoplasia on the affected side were identified in 17.9% and 38.4% of patients with CDH, respectively. CDH patients who exhibited these abnormalitiesshowed a poor outcome. Copyright (C) 2000 by W.B. Saunders Company.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 20/09/20 alle ore 00:35:44