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Titolo:
Intralobar bronchopulmonary sequestration in the newborn - a congenital malformation
Autore:
Laurin, S; Hagerstrand, I;
Indirizzi:
Univ Lund, Dept Radiol, S-22185 Lund, Sweden Univ Lund Lund Sweden S-22185 iv Lund, Dept Radiol, S-22185 Lund, Sweden Univ Lund, Dept Pathol, S-22185 Lund, Sweden Univ Lund Lund Sweden S-22185 iv Lund, Dept Pathol, S-22185 Lund, Sweden
Titolo Testata:
PEDIATRIC RADIOLOGY
fascicolo: 3, volume: 29, anno: 1999,
pagine: 174 - 178
SICI:
0301-0449(199903)29:3<174:IBSITN>2.0.ZU;2-D
Fonte:
ISI
Lingua:
ENG
Soggetto:
PULMONARY SEQUESTRATION; INFANTS;
Tipo documento:
Article
Natura:
Periodico
Settore Disciplinare:
Clinical Medicine
Citazioni:
24
Recensione:
Indirizzi per estratti:
Indirizzo: Laurin, S Univ Lund, Dept Radiol, S-22185 Lund, Sweden Univ Lund Lund Sweden S-22185 ept Radiol, S-22185 Lund, Sweden
Citazione:
S. Laurin e I. Hagerstrand, "Intralobar bronchopulmonary sequestration in the newborn - a congenital malformation", PEDIAT RAD, 29(3), 1999, pp. 174-178

Abstract

Background. Intralobar sequestration (ILS) has been suggested to be an acquired lesion. However, we have observed several young infants who had ILS. Objectives. Since this fact seems to indicate a congenital origin, we reviewed our experience. Material and Methods. A retrospective review of bronchopulmonary sequestration from the Departments of Radiology and Pathology in Lund between 1964 and 1997. Results. We identified seven infants or young children with a diagnosis ofintralobar sequestration. In each patient, the ILS was present before recurrent infection developed. Five had chest X-rays as neonates, one at 3 months and one at 11 months of age. All but one showed an abnormality on their first chest X-ray, consistent with sequestration. Six of the ILS were verified at angiography; all seven were surgically removed. Two of the children with ILS also had congenital cystic adenomatoid malformation (CCAM). Three children had both ILS and scimitar syndrome. Conclusions. The fact that ILS was present in seven newborn and young infants indicates that this lesion is, at least in some patients, a congenital malformation.

ASDD Area Sistemi Dipartimentali e Documentali, Università di Bologna, Catalogo delle riviste ed altri periodici
Documento generato il 23/09/20 alle ore 12:51:29