{"status":"ok","message-type":"work","message-version":"1.0.0","message":{"indexed":{"date-parts":[[2026,10,14]],"date-time":"2026-10-14T13:46:36Z","timestamp":1791985596328,"version":"4.4.0"},"reference-count":12,"publisher":"Ovid Technologies (Wolters Kluwer Health)","issue":"4","license":[{"start":{"date-parts":[[2026,10,1]],"date-time":"2026-10-01T00:00:00Z","timestamp":1790812800000},"content-version":"unspecified","delay-in-days":0,"URL":"http:\/\/creativecommons.org\/licenses\/by-nc-nd\/4.0"}],"content-domain":{"domain":["lww.com","ovid.com"],"crossmark-restriction":true},"short-container-title":[],"published-print":{"date-parts":[[2026,10]]},"abstract":"<jats:title>ABSTRACT<\/jats:title>\n                  <jats:p>Uncorrected tetralogy of Fallot (TOF) can be associated with widespread abnormalities, but the giant right atrium (RA) is an extremely rare one. The giant RA can cause additional problems causing atrial arrythmias, thromboembolism, and compression of adjacent structures. Tricuspid regurgitation is common with annular dilatation. In symptomatic cases, reduction atrioplasty is recommended. Sternotomy should be careful to avoid damage to the giant RA. In asymptomatic cases, anticoagulation should be carried out. We report a rare case of uncorrected TOF associated with the giant RA and got successfully treated with surgery.<\/jats:p>","DOI":"10.4103\/aca.aca_333_25","type":"journal-article","created":{"date-parts":[[2026,10,12]],"date-time":"2026-10-12T17:00:11Z","timestamp":1791824411000},"page":"634-637","update-policy":"https:\/\/doi.org\/10.1097\/lww.0000000000001000","source":"Crossref","is-referenced-by-count":0,"title":["An Extremely Rare Association of the Giant Right Atrium with Uncorrected Tetralogy of Fallot in an Adolescent Male Patient"],"prefix":"10.4103","volume":"29","author":[{"given":"Arupratan","family":"Maiti","sequence":"first","affiliation":[{"name":"Department of Cardiac Anaesthesia, Apollo Multispeciality Hospital, Kolkata, West Bengal, India"}],"role":[{"vocabulary":"crossref","role":"author"}]},{"given":"Amrita","family":"Guha","sequence":"additional","affiliation":[{"name":"Department of Cardiac Anaesthesia, Apollo Multispeciality Hospital, Kolkata, West Bengal, India"}],"role":[{"vocabulary":"crossref","role":"author"}]}],"member":"276","published-online":{"date-parts":[[2026,10,12]]},"reference":[{"key":"R1-20261014","first-page":"1740","article-title":"Congenital malformations of the right atrium and the coronary sinus","volume":"117","author":"Binder","year":"2000","journal-title":"Clin Chest Med"},{"key":"R2-20261014","first-page":"529","article-title":"Trans myocardial palpatory surgery of the heart","volume":"66","author":"Bailey","year":"1952","journal-title":"Can Med Assoc J"},{"key":"R3-20261014","first-page":"855","article-title":"Idiopathic dilation of the right atrium: Case report and survey of the literature","volume":"13","author":"Rutledge","year":"1997","journal-title":"Can J Cardiol"},{"issue":"2","key":"R4-20261014","doi-asserted-by":"crossref","first-page":"227","DOI":"10.1161\/01.CIR.40.2.227","article-title":"Sudden death in idiopathic (congenital) right atrial enlargement. 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