Persistent truncus arteriosus

Most of the time, this defect occurs spontaneously. Genetic disorders and teratogens (viruses, metabolic imbalance, and industrial or pharmacological agents) have been associated as possible causes. Up to 50% (varies in studies) of cases are associated with chromosome 22q11 deletions (DiGeorge Syndrome). The neural crest, specifically a population known as the cardiac neural crest, directly contributes to the aorticopulmonary septum.{{cite journal | vauthors = Kirby ML, Gale TF, Stewart DE | title = Neural crest cells contribute to normal aorticopulmonary septation | journal = Science | volume = 220 | issue = 4601 | pages = 1059–61 | date = June 1983 | pmid = 6844926 | doi = 10.1126/science.6844926 | bibcode = 1983Sci...220.1059K }}{{cite journal | vauthors = Jiang X, Rowitch DH, Soriano P, McMahon AP, Sucov HM | title = Fate of the mammalian cardiac neural crest | journal = Development | volume = 127 | issue = 8 | pages = 1607–16 | date = April 2000 | doi = 10.1242/dev.127.8.1607 | pmid = 10725237 }}

Microablation of the cardiac neural crest in developing chick embryos and genetic anomalies affecting this population of cells in rodents results in persistent truncus arteriosus.{{cite journal | vauthors = Hutson MR, Kirby ML | title = Neural crest and cardiovascular development: a 20-year perspective | journal = Birth Defects Research. Part C, Embryo Today | volume = 69 | issue = 1 | pages = 2–13 | date = February 2003 | pmid = 12768653 | doi = 10.1002/bdrc.10002 | doi-access = free }}{{cite journal | vauthors = Waller BR, McQuinn T, Phelps AL, Markwald RR, Lo CW, Thompson RP, Wessels A | title = Conotruncal anomalies in the trisomy 16 mouse: an immunohistochemical analysis with emphasis on the involvement of the neural crest | journal = The Anatomical Record | volume = 260 | issue = 3 | pages = 279–93 | date = November 2000 | pmid = 11066038 | doi = 10.1002/1097-0185(20001101)260:3<279::AID-AR65>3.0.CO;2-2 | s2cid = 45359927 | doi-access = free }}{{cite journal | vauthors = Franz T | title = Persistent truncus arteriosus in the Splotch mutant mouse | journal = Anatomy and Embryology | volume = 180 | issue = 5 | pages = 457–64 | year = 1989 | pmid = 2619088 | doi = 10.1007/BF00305120 | s2cid = 24116967 }}

Numerous perturbations affecting the cardiac neural crest have been associated with persistent truncus arteriosus, some of which include growth factors (fibroblast growth factor 8 and bone morphogenetic protein), transcription factors (T-box, Pax, Nkx2-5, GATA-6, and Forkhead), and gap junction proteins (Connexin). The cardiac neural crest also contributes the smooth muscle of the great arteries.{{citation needed|date=September 2020}}

Image:TruncusArteriosus.svg

Anatomical changes associated with this disorder includes:{{citation needed|date=September 2020}}

• single artery arising from the two ventricles which gives rise to both the aortic and pulmonary vessels
• abnormal truncal valve
• right sided aortic arch in about 30% of cases (not shown)
• large ventricular septal defect
• pulmonary hypertension
• complete mixing occurring at level of the great vessel
• right-to-left shunting of blood

The diagnosis is based on:{{cn|date=February 2021}}

• Cyanosis presents at birth
• Heart failure may occur within weeks
• Systolic ejection murmur is heard at the left sternal border
• Widened pulse pressure
• Bounding arterial pulses
• Loud second heart sound
• Biventricular hypertrophy
• Cardiomegaly
• Increased pulmonary vascularity
• Hypocalcemia (if associated with DiGeorge syndrome)

A well-known classification is the fourfold system developed by Collett and Edwards in 1949.Collett RW, Edwards JE: Persistent truncus arteriosus: a classification according to anatomic types. Surg Clin North Am 1949; 29: 1245-70. Collett/Edwards Types I, II, and III are distinguished by the branching pattern of the pulmonary arteries:{{cite web |url=https://www.merckmanuals.com/professional/pediatrics/congenital-cardiovascular-anomalies/persistent-truncus-arteriosus |title=Persistent Truncus Arteriosus: Congenital Cardiovascular Anomalies: Merck Manual Professional |access-date=2021-02-11 }}{{cite web |url=http://www.emedicine.com/ped/topic2316.htm |title=eMedicine - Truncus Arteriosus : Article by Doff McElhinney, MD |access-date=2007-11-04 }}

• Type I: The branch pulmonary arteries arise from a single "main pulmonary artery" arising from the lateral surface of the common trunk
• Type II: The branch pulmonary arteries arises separately, but near each other posteriorly off the common trunk
• Type III: The branch pulmonary arteries arise separately and far apart off the common trunk
• Type IV: The branch pulmonary arteries arise distally off the aorta, or the lungs are supplied by multiple aortopulmonary collaterals. Type IV is now considered a form of Tetralogy of Fallot and not Common Arterial Trunk.

Another well-known classification was defined by Stella and Richard Van Praagh in 1965.{{cite journal | vauthors = Van Praagh R, Van Praagh S | title = The anatomy of common aorticopulmonary trunk (truncus arteriosus communis) and its embryologic implications. A study of 57 necropsy cases | journal = The American Journal of Cardiology | volume = 16 | issue = 3 | pages = 406–25 | date = September 1965 | pmid = 5828135 | doi = 10.1016/0002-9149(65)90732-0 | doi-access = free }} In this classification scheme, the preceding letter ("A" or "B") refers to the presence or absence, respectively, of a ventricular septal defect. Type B common arterial trunk is extremely rare; so below, only Type A is considered:{{cn|date=October 2021}}

• Type A1: The branch pulmonary arteries arise from a single "main pulmonary artery" arising from the lateral surface of the common trunk (Collett & Edwards Type I)
• Type A2: The branch pulmonary arteries arise separately off the common trunk (includes both Collett & Edwards Types II and III).
• Type A3: One branch pulmonary artery arises off the common trunk, and one branch pulmonary artery is isolated, arising from a patent ductus arteriosus.
• Type A4: Common arterial trunk in association with interrupted aortic arch.

As both of the above schemes involve four numerals, they can be easily confused. For this reason, the Collette & Edwards scheme usually uses roman numerals while the Van Praagh system uses arabic numerals and the preceding "A". Ambiguity as to the system being used can lead to misunderstanding.

The classification in the International Paediatric and Congenital Cardiac Code (IPCCC) attempts to eliminate this source of confusion with the following nomenclature scheme, which removes the use of numbered types:

• Common arterial trunk with aortic dominance and both pulmonary arteries arising from trunk (includes Collette & Edwards Types I, II, and III and Van Praagh types 1 and 2).
• Common arterial trunk with aortic dominance and one pulmonary artery absent from trunk, isolated pulmonary artery (Van Praagh type 3).
• Common arterial trunk with pulmonary dominance and aortic arch obstruction (Van Praagh type 4)

Treatment is with neonatal surgical repair, with the objective of restoring a normal pattern of blood flow.{{cite journal | vauthors = Rodefeld MD, Hanley FL | title = Neonatal truncus arteriosus repair: surgical techniques and clinical management | journal = Seminars in Thoracic and Cardiovascular Surgery. Pediatric Cardiac Surgery Annual | volume = 5 | issue = 1 | pages = 212–7 | year = 2002 | pmid = 11994881 | doi = 10.1053/pcsu.2002.31497 }} The surgery is open heart, and the patient will be placed on cardiopulmonary bypass to allow the surgeon to work on a still heart. The heart is opened and the ventricular septal defect is closed with a patch. The pulmonary arteries are then detached from the common artery (truncus arteriosus) and connected to the right ventricle using a tube (a conduit or tunnel). The common artery, now separated from the pulmonary circulation, functions as the aorta with the truncal valve operating as the aortic valve. Most babies survive this surgical repair, but may require further surgery as they grow up. For example, the conduit does not grow with the child and may need to be replaced as the child grows. Furthermore, the truncal valve is often abnormal and may require future surgery to improve its function.

There have been cases where the condition has been diagnosed at birth and surgical intervention is an option. A number of these cases have survived well into adulthood.{{cite journal | vauthors = Haskal ZJ | title = SIR 2005 Annual Meeting Film Panel Case: hemoptysis and bronchial artery embolization in an adult with uncorrected truncus arteriosus and Eisenmenger syndrome | journal = Journal of Vascular and Interventional Radiology | volume = 16 | issue = 5 | pages = 635–8 | year = 2005 | pmid = 15872317 | doi = 10.1097/01.RVI.0000161372.87971.84 }}

Persistent truncus arteriosus is a rare cardiac abnormality that has a prevalence of less than 1%.{{cite journal | vauthors = Barata IA | title = Cardiac emergencies | journal = Emergency Medicine Clinics of North America | volume = 31 | issue = 3 | pages = 677–704 | date = August 2013 | pmid = 23915599 | doi = 10.1016/j.emc.2013.04.007 }}{{cite journal | vauthors = Parker SE, Mai CT, Canfield MA, Rickard R, Wang Y, Meyer RE, Anderson P, Mason CA, Collins JS, Kirby RS, Correa A | title = Updated National Birth Prevalence estimates for selected birth defects in the United States, 2004-2006 | journal = Birth Defects Research. Part A, Clinical and Molecular Teratology | volume = 88 | issue = 12 | pages = 1008–16 | date = December 2010 | pmid = 20878909 | doi = 10.1002/bdra.20735 }}

Image:Gray469.png|Diagrams to illustrate the transformation of the bulbus cordis. Ao. Truncus arteriosus. Au. Atrium. B. Bulbus cordis. RV. Right ventricle. LV. Left ventricle. P. Pulmonary artery.

• Truncus arteriosus (embryology)
• Patent ductus arteriosus

{{Reflist}}

• [https://www.ncbi.nlm.nih.gov/pubmedhealth/PMH0002101/ A.D.A.M. Medical Encyclopedia] from NCBI site.
• [https://www.gosh.nhs.uk/conditions-and-treatments/conditions-we-treat/truncus-arteriosus/ Truncus arteriosus]

{{Medical resources

| ICD10 = {{ICD10|Q|20|0|q|20}}

| ICD9 = {{ICD9|745.0}}

| ICDO =

| OMIM = 217095

| DiseasesDB = 32081

| MedlinePlus = 001111

| eMedicineSubj = ped

| eMedicineTopic = 2316

| MeshID = D014339

}}

{{Congenital malformations and deformations of circulatory system}}

{{DEFAULTSORT:Persistent Truncus Arteriosus}}

Category:Congenital heart defects

Category:Rare diseases