Total anomalous pulmonary venous connection pathophysiology

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Cafer Zorkun, M.D., Ph.D. [2]; Keri Shafer, M.D. [3]; Priyamvada Singh, MBBS[4]; Assistant Editor-In-Chief: Kristin Feeney, B.S. [5]

Overview

In patients of total anomalous pulmonary venous connection (TAPVC) there is a mixing of oxygenated pulmonary venous blood with deoxygenated blood from systemic circulation.

Pathophysiology

Mixing of blood could occur at three levels i.e. supracardiac, infracardiac and cardiac. In the former two the mixing occurs outside the heart and in latter inside the heart (right atrium).

This mixed deoxygenated blood is shunted from right-to-left side of heart (patent foramen ovale, atrial septal defect or patent ductus arteriosus). This right to left shunting causes cyanosis in the patient.

Since, the right side of heart is receiving blood both from pulmonary and systemic circulation it leads to development of pulmonary hypertension, right atrial and ventricular hypertrophy.

Obstructive forms: In the supracardiac form of TAPVC, the obstruction can occur by compression of the ascending vertical vein between the left main stem bronchus and left pulmonary artery. It can also occur as narrowing at the insertion of the vertical vein into the innominate vein. Obstruction is present in almost all cases of infracardiac TAPVC but is uncommon in the cardiac form.

Images

Normal heart[1]
Total anomalous pulmonary venous connection[2]

Genetic

Genetic mutations associated with total anomalous pulmonary venous connection include:[3][4]

Associated Disorders

Gross Pathology

cardiac type of TAPVC with opening of cardiac vein into right atrium
supracardiac type of TAPVC with connecting vertical vein



Video

Unobstructed forms: No significant stenosis of the pulmonary veins. {{#ev:youtube|eODH6E_OA_M}}

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References

  1. https://www.cdc.gov/ncbddd/heartdefects/tapvr.html
  2. https://commons.wikimedia.org/wiki/File:Tapv-575px.jpg#/media/File:Tapv-575px.jpg
  3. Phelan, K.; McDermid, H.E. (2011). "The 22q13.3 Deletion Syndrome (Phelan-McDermid Syndrome)". Molecular Syndromology. doi:10.1159/000334260. ISSN 1661-8777.
  4. Bleyl, Steven B.; Saijoh, Yukio; Bax, Noortje A.M.; Gittenberger-de Groot, Adriana C.; Wisse, Lambertus J.; Chapman, Susan C.; Hunter, Jennifer; Shiratori, Hidetaka; Hamada, Hiroshi; Yamada, Shigehito; Shiota, Kohei; Klewer, Scott E.; Leppert, Mark F.; Schoenwolf, Gary C. (2010). "Dysregulation of the PDGFRA gene causes inflow tract anomalies including TAPVR: integrating evidence from human genetics and model organisms". Human Molecular Genetics. 19 (7): 1286–1301. doi:10.1093/hmg/ddq005. ISSN 0964-6906.

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