Tetralogy of Fallot

Tetralogy of Fallot is a congenital cardiac malformation that consists of an interventricular communication, also known as a ventricular septal defect, obstruction of the right ventricular outflow tract, override of the ventricular septum by the aortic root, and right ventricular hypertrophy.

Splenomegaly

Abnormal increased size of the spleen.


Total: 2

                       


(per page)
PMID (PMCID)
24865822
 FEMALE
Splenic hamartomas in Alagille syndrome: case report and literature review.
James AW, Nguyen A, Said J, Genshaft S, Lassman CR, Teitell M.
Fetal Pediatr Pathol. 2014;33(4):216-25.
Autopsy findings included growth restriction, Tetralogy of Fallot, paucity of intrahepatic bile ducts, end-stage renal disease with mesangiolipidosis, and splenomegaly with two well-circumscribed, splenic tumors.
9198297
 MALE
Cockayne syndrome with tetralogy of Fallot: a case report.
Choong CS, Liew KL, Huang YF, Chiu PC, Hsieh KS.
Zhonghua Yi Xue Za Zhi (Taipei). 1997;59(3):199-203.
This is a description of a three-year-old boy with typical features of Cockayne syndrome complicated with tetralogy of Fallot, pneumonia and hepato-splenomegaly.