Truncus arteriosus

Truncus arteriosus (TA) is a rare congenital cardiovascular anomaly characterized by a single arterial trunk arising from the heart by means of a single semilunar valve (<I>i.e.</I> truncal valve). Pulmonary arteries originate from the common arterial trunk distal to the coronary arteries and proximal to the first brachiocephalic branch of the aortic arch. TA typically overrides a large outlet ventricular septal defect (VSD). The intracardiac anatomy usually displays situs solitus and atrioventricular (AV) concordance.

Ventricular septal defect

A hole between the two bottom chambers (ventricles) of the heart. The defect is centered around the most superior aspect of the ventricular septum.


Total: 31

                      


(per page)
PMID (PMCID)
28386986
FEMALE Adult
Thrombus formation in the interrupted segment of the aorta.
Karavelioglu Y, Kalck M, Yetim M, Dogan T, Golbas Z.
Echocardiography. 2017;34(6):945-946.
It is usually associated with other cardiac anomalies, including ventricular septal defect, ductus arteriosus, and truncus arteriosus.
26803197
MIXED_SAMPLE
Cardiac-gated computed tomography angiography in three alpacas with complex congenital heart disease.
Stieger-Vanegas SM, Scollan KF, Meadows L, Sisson D, Schlipf J, Riebold T, Lohr CV.
J Vet Cardiol. 2016;18(1):88-98.
All three crias were subsequently diagnosed with complex cardiac defects including pulmonary atresia with a ventricular septal defect (VSD), a truncus arteriosus with a large VSD, and a double outlet right ventricle with a large VSD and aortic hypoplasia.
27098067
(4839129)
MALE Infant
Neonatal diabetes and protein losing enteropathy: a case report.
McMillan T, Girgis R, Sellers EA.
BMC Med Genet. 2016;17:32.
We report the case of a Caucasian male infant diagnosed shortly after birth with neonatal diabetes, truncus arteriosus type III, ventricular septal defect, atrial septal defect, an absent gallbladder and a right inguinal hernia.
24357125
MIXED_SAMPLE Infant
Deletions in 14q24.1q24.3 are associated with congenital heart defects, brachydactyly, and mild intellectual disability.
Oehl-Jaschkowitz B, Vanakker OM, De Paepe A, Menten B, Martin T, Weber G, Christmann A, Krier R, Scheid S, McNerlan SE, McKee S, Tzschach A.
Am J Med Genet A. 2014;164A(3):620-6.
While some clinical problems such as intestinal malrotation, cryptorchidism, and ectopic kidney were only observed in single patients, all three patients had mild intellectual disability, congenital heart defects (truncus arteriosus, pulmonary atresia, atrial septal defect, and/or ventricular septal defect), brachydactyly, hypertelorism, broad nasal bridge, and thin upper lips.
25926908
FEMALE
The quadricuspid aortic valve.
Franco A, Gabriel S, Ruehm SG.
J Radiol Case Rep. 2014;8(11):25-9.
We present a case of quadricuspid aortic valve associated with truncus arteriosus, ventricular septal defect, and interrupted aortic arch.
23626446
(3634258)
OTHER
Unusual association of aortic valve stenosis with ventricular septal defect and pulmonary atresia: Differentiation from truncus arteriosus with truncal valve stenosis.
Kumar SM, Bijulal S, Sivasankaran S.
Ann Pediatr Cardiol. 2013;6(1):87-9.
Unusual association of aortic valve stenosis with ventricular septal defect and pulmonary atresia: Differentiation from truncus arteriosus with truncal valve stenosis.
23626446
(3634258)
OTHER
Unusual association of aortic valve stenosis with ventricular septal defect and pulmonary atresia: Differentiation from truncus arteriosus with truncal valve stenosis.
Kumar SM, Bijulal S, Sivasankaran S.
Ann Pediatr Cardiol. 2013;6(1):87-9.
Here we describe a neonate with pulmonary atresia, ventricular septal defect and associated aortic valve stenosis and discuss the points of differentiation from truncus arteriosus.
22380655
MIXED_SAMPLE Adult
Prenatal diagnosis of a 22q11 deletion in a second-trimester fetus with conotruncal anomaly, absent thymus and meningomyelocele: Kousseff syndrome.
Canda MT, Demir N, Bal FU, Doganay L, Sezer O.
J Obstet Gynaecol Res. 2012;38(4):737-40.
The scan revealed a male fetus with truncus arteriosus, membranous ventricular septal defect, absent thymus and sacral meningomyelocele.
23091754
(3472535)
OTHER
Three-dimensional ultrasound findings in cornelia de lange syndrome: a case report.
Akahori Y, Masuyama H, Masumoto Y, Hiramatsu Y.
Case Rep Obstet Gynecol. 2012;2012:568351.
Further sonography diagnosis on cardiac abnormalities diagnosed the existence of ventricular septal defect in the outflow tract, atrioventricularis communis, and truncus arteriosus communis where the pulmonary artery branched from the common arterial trunk.
23091754
(3472535)
OTHER
Three-dimensional ultrasound findings in cornelia de lange syndrome: a case report.
Akahori Y, Masuyama H, Masumoto Y, Hiramatsu Y.
Case Rep Obstet Gynecol. 2012;2012:568351.
Further sonography diagnosis on cardiac abnormalities diagnosed the existence of ventricular septal defect in the outflow tract, atrioventricularis communis, and truncus arteriosus communis where the pulmonary artery branched from the common arterial trunk.
20830788
MIXED_SAMPLE Infant, Newborn
Anomalous subaortic left brachiocephalic vein in surgical cases and literature review.
Nagashima M, Shikata F, Okamura T, Yamamoto E, Higaki T, Kawamura M, Ryugo M, Izutani H, Imagawa H, Uchita S, Okamura Y, Suzuki H, Nakamura Y, Tagusari O, Kawachi K.
Clin Anat. 2010;23(8):950-5.
In patients with CHD, 73.3% (11 of 15) of the patients had conotruncal cardiac anomalies such as tetralogy of Fallot, ventricular septal defect with pulmonary atresia, truncus arteriosus, and interruption of the aortic arch.
20082465
MIXED_SAMPLE
Pancreatic hypoplasia presenting with neonatal diabetes mellitus in association with congenital heart defect and developmental delay.
Balasubramanian M, Shield JP, Acerini CL, Walker J, Ellard S, Marchand M, Polak M, Vaxillaire M, Crolla JA, Bunyan DJ, Mackay DJ, Temple IK.
Am J Med Genet A. 2010;152A(2):340-6.
In addition, Patient 1 had a ventricular septal defect, patent ductus arteriosus and pulmonary artery stenosis; Patient 2 had a truncus arteriosus and Patient 3 had tetralogy of Fallot.
20103368
MALE Infant, Newborn
Successful staged Fontan completion for truncus arteriosus with hypoplastic left ventricle.
Hoashi T, Bove EL, Ohye RG.
Ann Thorac Surg. 2010;89(2):635-7.
We report a case of truncus arteriosus type II with a large outlet ventricular septal defect and a hypoplastic left ventricle.
19564508
OTHER
Persistent truncus arteriosus with dissecting aneurysm and subsequent cardiac tamponade in a lamb.
Haist V, von Altrock A, Beineke A.
J Vet Diagn Invest. 2009;21(4):543-6.
This rare cardiac malformation was characterized by the presence of a common arterial trunk arising from the right ventricle and overriding a ventricular septal defect.
18400613
MIXED_SAMPLE Infant, Newborn
Crossed pulmonary arteries: report of two cases with emphasis on three-dimensional helical computed tomographic imaging.
Chen BB, Hsieh HJ, Chiu IS, Chen SJ, Wu MH.
J Formos Med Assoc. 2008;107(3):265-9.
Cardiac CT showed crossed pulmonary arteries, truncus arteriosus, type A interruption of the aortic arch, a ventricular septal defect, an atrial septal defect, and a large patent ductus arteriosus.
17726319
FEMALE
Severe pregnancy-induced deterioration of truncal valve regurgitation in an adolescent patient with repaired truncus arteriosus.
Hoendermis ES, Drenthen W, Sollie KM, Berger RM.
Cardiology. 2008;109(3):177-9.
Truncus arteriosus, a rare and complex congenital heart disease, is hallmarked by a single great vessel (truncus) that arises over a large ventricular septal defect and provides both the pulmonary and systemic circulation.
16856450
FEMALE Infant
The first pediatric case of Staphylococcus aureus with heterogenous resistant to vancomycin endocarditis in Thailand.
Phongsamart W, Srifeungfung S, Tiensasitorn C, Vanprapar N, Chearskul S, Chokephaibulkit K.
J Med Assoc Thai. 2005;88 Suppl 8:S264-8.
A 4 months old girl with truncus arteriosus type IV and ventricular septal defect developed methicillin-resistant S. aureus (MRSA) bacteremia and endocarditis after total repair operation.
14692650
FEMALE
Facio-auriculo-vertebral sequence in association with DiGeorge sequence, Rokitansky sequence, and Dandy-Walker malformation: case report.
Pillay K, Matthews LS, Wainwright HC.
Pediatr Dev Pathol. 2003;6(4):355-60.
Internal examination showed hypoplastic thymus and lungs, a type I truncus arteriosus, and ventricular septal defect.
12533811
FEMALE Adult
Prenatal diagnosis of mosaic ring chromosome 22 associated with cardiovascular abnormalities and intrauterine growth restriction.
Chen CP, Chern SR, Chang TY, Lee CC, Chen LF, Tzen CY, Wang W, Lin CJ, Yang BP, Yang LS.
Prenat Diagn. 2003;23(1):40-3.
Abnormal fetal sonographic findings included small for gestational age, a ventricular septal defect, and truncus arteriosus.
11716333
FEMALE Adult
Pulmonary arterial aneurysm with CATCH 22 syndrome--a case report.
Kinoshita O, Mizoue T, Kusama A, Gomi E, Sato S, Hongo M, Kubo K.
Angiology. 2001;52(11):789-91.
CATCH 22 syndrome is a developmental malformation caused by hemizygous deletion of 22q11 chromosome, which usually presents with cardiac malformation including tetralogy of Fallot, truncus arteriosus, patent arterial duct, and ventricular septal defect.