Cardiac Teratoma



Fig. 20.1
Single frontal view of the chest showing a mass along the left heart border and marked irregularity along the left mediastinum in a teenage patient with a mediastinal teratoma





20.2.2 ECG Findings


There are no specific ECG criteria [2].


20.2.3 CT Findings






  • Heterogeneous cardiac tumor


  • May see pericardial effusion


  • Presence of fat or calcifications [1]


20.2.4 MRI Findings






  • Multilobulated solid or cystic mass


  • May be hypointense on first-pass myocardial perfusion (FPP)


  • May demonstrate limited to no perfusion


  • May be isointense or hypointense on T1 and hyperintense on T2 [3, 4]


20.2.5 Echocardiography Findings






  • Solid heterogeneous mass with pericardial effusion [4]


20.2.6 Imaging Recommendations


Cardiac CT or MRI with contrast is recommended as the best imaging tool. Prenatal ultrasound is a good imaging tool and may show pericardial effusion.



20.3 Differential Diagnosis






  • Rhabdomyoma


  • Metastatic disease


  • Rhabdomyosarcoma


  • Myxoma


  • Fibroma


20.4 Pathology



20.4.1 Etiology


Teratomas contain all three germ cell layers (endoderm, ectoderm, and mesoderm), but their etiology is unknown.


20.4.2 Frequency


Teratomas are the second most common cardiac tumor in fetuses and neonates, in which they comprise 15–19 % of cardiac tumors [5]. They are rare outside the neonatal period. The male-to-female ratio is 2:1.


20.4.3 Gross Pathologic and Surgical Features


Macroscopic features include a cystic, lobular mass. The tumor is more often pericardial in location, not myocardial [6].

Only gold members can continue reading. Log In or Register to continue

Stay updated, free articles. Join our Telegram channel

Aug 12, 2017 | Posted by in CARDIOLOGY | Comments Off on Cardiac Teratoma

Full access? Get Clinical Tree

Get Clinical Tree app for offline access