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THE JOURNAL OF CARDIOVASCULAR SURGERY

Rivista di Chirurgia Cardiaca, Vascolare e Toracica


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The Journal of Cardiovascular Surgery 2001 April;42(2):197-9

lingua: Inglese

Aortopulmonary window coexisting with tetralogy of Fallot

Alborino D., Guccione P., Di Donato R., Marino B.

From the Depart­ment of Car­di­ology and Car­diac Sur­gery Bam­bino ­Gesù ­Children’s Hos­pital, ­Rome, ­Italy


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Aor­to­pul­mo­nary ­window is a ­rare car­diac mal­for­ma­tion pre­senting ­either in the iso­lated ­form, or in asso­ci­a­tion ­with ­other car­diac anom­a­lies. The iso­lated ­form usu­ally ­presents an ­increased pul­mo­nary ­blood ­flow as the ­main clin­ical fea­ture, but if asso­ciated ­with ­other car­diac anom­a­lies the clin­ical find­ings ­change ­according to the addi­tional ­defect. ­Only 19 ­cases of aor­to­pul­mo­nary ­window asso­ciated ­with tet­ralogy of ­Fallot ­have ­been ­reported. ­Five of ­them ­have asso­ciated pul­mo­nary ­atresia. We ­report two neo­natal ­cases of aor­to­pul­mo­nary ­window and tet­ralogy of ­Fallot, one of ­them pre­senting an asso­ciated pul­mo­nary ­atresia.

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