Journals / Turkish Journal of Pediatrics / 2019 / Cilt: 61 - Sayı: 2

Fetal intrapericardial teratomas

Pages
153–158
DOI
—
🏛️Bibliographic metadata and full text access for this article are provided via DergiPark.
DergiPark Record ↗
✨

AI Summary & Key Takeaways

AI Insight
⚡ TL;DR(Too Long; Didn't Read)

As a result, the fetoneonatal outcomesare somewhat promising.

📌 3 Key Takeaways

🎯
Objective & Hypothesis:Fetal intrapericardial teratomas are rare and benign.
📊
Key Findings & Data:It was noteworthy that fetal pericardial/pleuraleffusions or ascites were detected since 19-week gestation, and tumors couldbe found since 21-week gestation.
💡
Conclusion & Impact:As a result, the fetoneonatal outcomesare somewhat promising.
🔬Design:Review & Systematic Survey
📍Scope:Comprehensive Sample
⚙️Variables:Domain Parameters

Özet

Fetal intrapericardial teratomas are rare and benign. However, they canbe life-threatening owing to the complicated massive pericardial effusions,tamponade, or cardiorespiratory distress. The purpose of this review is togive an overview on clinical features, management and prognoses of fetalintrapericardial teratomas. The materials of this study were based on acomprehensive literature retrieval of fetal intrapericardial teratomas publishedin the past two decades. It was noteworthy that fetal pericardial/pleuraleffusions or ascites were detected since 19-week gestation, and tumors couldbe found since 21-week gestation. A growing trend of tumors was observed inmore than half of the cases. Prenatal centesis and postnatal tumor resectionwere required in most of the cases. Fetoneonatal deaths (including fetaldemise, termination of pregnancy and neonatal death) occurred in one-thirdof the cases. The neonatal survival rate was 59.4%. Symptomatic fetusesusually required perinatal maneuvers, such as pericardiocentesis, or thoraco-/pericardio-amniotic shunt in order to improve fetal hemodynamic status andprolong the pregnancy for lung maturity. Open fetal surgery and ex uterointrapartum treatment (EXIT) procedure can be considered, however, impactof EXIT procedure on later delivery remains uncertain. Postnatal operationis a curative and symptom-relieving method for those cases with prenatallydiagnosed intrapericardial teratomas. As a result, the fetoneonatal outcomesare somewhat promising.

🔖

Cite This Article

YUAN, S. M., LİN, H. (2019). Fetal intrapericardial teratomas. Turkish Journal of Pediatrics, Cilt: 61 - Sayı: 2, 153–158. https://ajindex.com/articles/412042

📄 Full Text PDF Viewer

📄

PDF görüntüleyici hazırlanıyor...

References (9)

  1. Banfield F, Dick M 2nd, Behrendt DM, Rosenthal A, Pescheria A, Scott W. Intrapericardial teratoma: a new and treatable cause of hydrops fetalis. Am J Dis Child 1980; 134: 1174-1175
  2. Beghetti M, Prieditis M, Rebeyka IM, Mawson J. Images in cardiovascular medicine. Intrapericardial teratoma. Circulation 1998; 97: 1523-1524
  3. Yuan SM. Cardiac etiologies of hydrops fetalis. Z Geburtshilfe Neonatol 2017; 221: 67-72
  4. Yuan SM. Fetal primary cardiac tumors during perinatal period. Pediatr Neonatol 2017; 58: 205-210
  5. Kulthe SG, Nadkarni UB, Singh A, Deshmukh CT, Jain MK, Shah MD. Recurrent cardiac tamponade: intrapericardial teratoma. Indian Pediatr 1995; 32: 88-91
  6. Aldousany AW, Joyner JC, Price RA, Boulden T, Watson D, Disessa TG. Diagnosis and treatment of intrapericardial teratoma. Pediatr Cardiol 1987; 8: 51-53
  7. Agarwal A, Rosenkranz E, Yasin S, Swaminathan S. EXIT procedure for fetal mediastinal teratoma with large pericardial effusion: a case report with review of literature. J Matern Fetal Neonatal Med 2018; 31: 1099-1103
  8. Bader R, Hornberger LK, Nijmeh LJ, et al. Fetal pericardial teratoma: presentation of two cases and review of literature. Am J Perinatol 2006; 23: 53-58
  9. Cavalcante CTMB, Pinto Júnior VC, Pompeu RG, et al. Early treatment of intrapericardial teratoma: A case presentation and systematic literature review. J Matern Fetal Neonatal Med 2019; 32: 2262-2268. 10.Cetrano E, Polito A, Carotti A. Primitive intrapericardial teratoma associated with yolk sac tumour. Cardiol Young 2015; 25: 158-160. 11.Czernik C, Stiller B, Hübler M, Hagen A, Henrich W. Hydrops fetalis caused by a large intrapericardial teratoma. Ultrasound Obstet Gynecol 2006; 28: 973-976. 12.Daniels CJ, Cohen DM, Phillips JR, Rowland DG. Prenatal detection of a pericardial teratoma. Circulation 1999; 99: E1-E2. 13.de Bustamante TD, Azpeitia J, Miralles M, Jiménez M, Santos-Briz A, Rodríguez-Peralto JL. Prenatal sonographic detection of pericardial teratoma. J Clin Ultrasound 2000; 28: 194-198. 14.Devlieger R, Hindryckx A, Van Mieghem T, et al. Therapy for foetal pericardial tumours: survival following in utero shunting, and literature review. Fetal Diagn Ther 2009; 25: 407-412. 15.Fagiana AM, Barnett S, Reddy VS, Milhoan KA. Management of a fetal intrapericardial teratoma: a case report and review of the literature. Congenit Heart Dis 2010; 5: 51-55. 16.Goldberg SP, Boston US, Turpin DA, et al. Surgical management of intrapericardial teratoma in the fetus.