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The pathological diagnosis of pulmonary atresia with abnormal ventriculoarterial connections in the fetus

Published online by Cambridge University Press:  19 August 2008

Lona Jane Mary Jeffrey*
Affiliation:
From the Departments of HistopathologySt George's Hospital
Siew Yen Ho
Affiliation:
The Department of PaediatricsNational Heart and Lung Institute, London
Deborah Peta Murray Moncrieff
Affiliation:
The Department of Obstetrics and GynaecologySt Helier Hospital, Carshalton
Leslie David Ross
Affiliation:
The Department of Obstetrics and GynaecologySt Helier Hospital, Carshalton
John Malcolm Pearce
Affiliation:
The Department of Obstetrics, St George's Hospital
*
Dr. Iona Jane Mary Jeffrey, Department of Histopathology, St George's Hospital, Tooting, London SW17 ORE, United Kingdom. Tel.081 672 9944; Fax. 081 767 8326.

Abstract

Pulmonary atresia with abnormal ventriculoarterial connections in the presence of an intact ventricular septum is rare even in postnatal life. Two cases are described in which this combination of lesions was diagnosed in previable fetuses at autopsy. Both pregnancies were terminated for gross structural abnormalities discovered on antenatal ultrasound scans. In the first case, the pulmonary atresia was associated with intact ventricular septum, a double outlet left ventricle and hypoplasia of the tricuspid valve, right ventricle and arterial duct, a combination of lesions that would appear to be unique. In the second case, there was complete transposition and a hypoplastic left ventricle. The severity of the cardiac lesions in both fetuses was such that it is unlikely that either would have survived to term. In the first case no other malformation was present, but in the second there was also a large encephalocoele secondary to early amnion rupture, and a single umbilical artery. The association of the cardiac lesion with early amnion rupture in this second fetus would appear to be a chance event.

Type
Original Articles
Copyright
Copyright © Cambridge University Press 1993

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References

title

1.Allan, LDCook, A. Pulmonary atresia with intact ventricular septum in the fetus. Cardiol Young 1992; 2: 367376.CrossRefGoogle Scholar
2.Brandt, PWTCalder, ALBarratt–Boyes, BGNeutze, JM. Double outlet left ventricle. Morphology, cineangiocardio graphic diagnosis and surgical treatment. Am J Cardiol 1976; 38: 897909.CrossRefGoogle Scholar
3.Bharati, SLev, MStewart, RMcAllister, HAKirklin, JW. Themorphological spectrum of double outlet left ventricle and its surgical significance. Circulation 1978; 58: 558565.CrossRefGoogle Scholar
4.Otero, Coto EQuero, Jimenez MAnderson, RHCastafleda, ARFreedom, RMAttic, FKreutzer, EKreutzer, GBecker, AE. Double outlet left ventricle. In Anderson, RHMaCartney, FJShinebourne, EA, Tynan, M. (eds). Paediatric Cardiology. Churchill Livingstone. Edinburgh, 1983, pp 451465.Google Scholar
5.Paul, MHMuster, AJSinha, SNCole, RBVan Praagh, R. Double–outlet left ventricle with an intact ventricular septum. Circulation 1970; 41: 129139.CrossRefGoogle ScholarPubMed
6.Lang, DHoffstetter, RKupferschmnid, C. Hypoplastic left heart with complete transposition of the great arteries. Br Heart J 1985; 53: 650653.CrossRefGoogle ScholarPubMed
7.Ho, SYAngelini, ARussell, G. Pulmonary atresia with hyp oplastic left ventricle. Int J Cardiol 1987; 15: 349352.CrossRefGoogle Scholar