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Unobstructed infracardiac total anomalous pulmonary venous connection in a 7-month-old infant: A rare case report.
Shhada, Eman; Nahle, Ali Alakbar; Hamdar, Hussein; Jawad, Ali; Hasan, Hasan; Hamra, Mohammad Shadi; Saleh, Mohannad; Al-Dairy, Alwaleed; Daood, Huda.
Affiliation
  • Shhada E; Pediatric Intensive Care Department, Faculty of Medicine, Children's Hospital Damascus University Damascus Syria.
  • Nahle AA; Faculty of Medicine Damascus University Damascus Syria.
  • Hamdar H; Faculty of Medicine Damascus University Damascus Syria.
  • Jawad A; Faculty of Medicine Damascus University Damascus Syria.
  • Hasan H; Department of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus Syria.
  • Hamra MS; Department of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus Syria.
  • Saleh M; Department of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus Syria.
  • Al-Dairy A; Department of Cardiac Surgery, Faculty of Medicine, Pediatric Cardiac Surgery Unit Damascus University Damascus Syria.
  • Daood H; Pediatric Intensive Care Department, Faculty of Medicine, Children's Hospital Damascus University Damascus Syria.
Clin Case Rep ; 11(10): e8079, 2023 Oct.
Article in En | MEDLINE | ID: mdl-37854257
ABSTRACT
Key Clinical Message This case underscores the importance of early detection and treatment for total anomalous pulmonary venous connection, a rare congenital heart condition, through comprehensive newborn physical exams and prompt specialist referrals. Abstract Total anomalous pulmonary venous connection (TAPVC) is a rare form of congenital heart disease that is typically diagnosed in neonates. TAPVC has four subtypes, with the infracardiac type at risk of obstruction. TAPVC is usually diagnosed in newborns but can occur in other age groups. In this case, a 7-month-old male with recurrent cyanotic episodes was diagnosed with TAPVC of the infracardiac type using computed tomography angiography. The patient underwent successful surgical repair with a favorable postoperative course and was discharged in stable condition, and further follow-up was not possible beyond 2 months. This case emphasizes the importance of early recognition and management of this condition to prevent the progression of subsequent complications.
Key words

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Case Rep Year: 2023 Document type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Language: En Journal: Clin Case Rep Year: 2023 Document type: Article
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