Persistent Eustachian valve and transient arterial hypoxemia in a newborn: a clinical observation

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Abstract

The Eustachian valve (EV) is located in the orifice of inferior vena cava and belongs to structures of the normal heart. It plays an important role in the fetal blood flow by directing the flow of blood from inferior vena cava through an open foramen ovale to the left atrium, thereby ensuring the systemic flow in a fetus and bypassing the pulmonary circulation. After birth and upon closure of the foramen ovale, the valve ceases to function and tends to regress. Usually, a prominent EV is a clinically non-significant ultrasound finding. In isolated cases, however, it can cause significant hemodynamic abnormalities and subsequent rhythm disorders, delayed fetal development and transient hypoxemia in newborns. It can extremely rare be a cause of blood right-toleft shunting through the foramen ovale leading to desaturation. Clinically it can manifest by central cyanosis in newborns and infants. The differential diagnosis is made in neonatal intensive care units. We present a  case of transient arterial hypoxemia in a  newborn with prominent EV and inter-atrial shunt. A  one-month old infant was transferred from the Department of Pediatric Cardiology with a  history of transient hypoxemic spells related to right-to-left shunting via atrial septal defect caused by obstruction of the tricuspid valve by the prominent EV. The instrumental findings including contrast-enhanced tomography supported this hypothesis. The patient was stable for subsequent 10 days of the follow-up, which allowed for further conservative managements until the conventional time point for children with an atrial septal defect. Potential regress of the prominent EV, as well as natural growth of an infant and his/hers intracardiac structures, provide mostly favorable outcome without a surgical intervention. This was clearly illustrated in the clinical case.

About the authors

M. V. Tarayan

Moscow Regional Research and Clinical Institute (MONIKI)

Author for correspondence.
Email: tarayan@mail.ru
ORCID iD: 0000-0003-4620-1679

Marat V. Tarayan – MD, PhD, Cardiovascular Surgeon, Department of Cardiosurgery

61/2–5 Shchepkina ul., Moscow, 129110

Россия

A. I. Drozdova

Research and Clinical Institute of Children

Email: fake@neicon.ru

Alfiya I. Drozdova – Head of Department of Pediatric Cardiology

62 Bol'shaya Serpukhovskaya ul., Moscow, 115093

Россия

I. O. Bondareva

Moscow Regional Research and Clinical Institute (MONIKI)

Email: fake@neicon.ru

Irina O. Bondareva – Pediatric Cardiologist, Department of Cardiosurgery

61/2 Shchepkina ul., Moscow, 129110

Россия

E. S. Efremov

Moscow Regional Research and Clinical Institute (MONIKI)

Email: fake@neicon.ru

Evgeniy S. Efremov – Cardiovascular Surgeon, Department of Cardiosurgery

61/2 Shchepkina ul., Moscow, 129110

Россия

M. V. Vishnyakova

Moscow Regional Research and Clinical Institute (MONIKI)

Email: fake@neicon.ru
ORCID iD: 0000-0003-3838-636X

Marina V. Vishnyakova – MD, PhD, Head of Department of X-ray Diagnostics

61/2 Shchepkina ul., Moscow, 129110

Россия

References

  1. Loukas M, Sullivan A, Tubbs RS, Weinhaus AJ, Derderian T, Hanna M. Chiari's network: review of the literature. Surg Radiol Anat. 2010;32(10):895–901. doi: 10.1007/s00276-010-0639-z.
  2. Bhatnagar KP, Nettleton GS, Campbell FR, Wagner CE, Kuwabara N, Muresian H. Chiari anomalies in the human right atrium. Clin Anat. 2006;19(6):510–516. doi: 10.1002/ca.20195.
  3. Watson T, Kakar P, Srivastava S, Dhanjal TS. Eustachian valve remnant. Cardiol J. 2007;14(5): 508–509.
  4. Gussenhoven WJ, Essed CE, Bos E. Persistent right sinus venosus valve. Br Heart J. 1982;47(2):183–185. doi: 10.1136/hrt.47.2.183.
  5. Lanzarini L, Lucca E. Persistence of the right valve of the sinus venosus resulting in an unusually prominent Chiari network remnant mimicking cor triatriatum dexter. Pediatr Cardiol. 2002;23(1):103–105. doi: 10.1007/s00246-001-0027-x.
  6. Trento A, Zuberbuhler JR, Anderson RH, Park SC, Siewers RD. Divided right atrium (prominence of the eustachian and thebesian valves). J Thorac Cardiovasc Surg. 1988;96(3): 457–463.
  7. Akçaboy MI, Ekici F, Tutar E. Unusually redundant Chiari network. Pediatr Cardiol. 2006;27(4):525–526. doi: 10.1007/s00246-006-6007-4.
  8. Chiari H. Über Netzbildungen im rechten Vorhof des Herzens. Beitr Pathol Anat. 1897;22:1– 10.
  9. Bendadi F, van Tijn DA, Pistorius L, Freund MW. Chiari's network as a cause of fetal and neonatal pathology. Pediatr Cardiol. 2012;33(1): 188–191. doi: 10.1007/s00246-011-0114-6.
  10. Arenas Ramírez J, Fernandez Castro C, Otero Chouza M, Duplá Parugues B, Montes Sanchez R. Persistent and redundant eustachian valve simulating atrial tumor: prenatal diagnosis. Ultrasound Obstet Gynecol. 2007;29(6): 704–707. doi: 10.1002/uog.3992.
  11. Clements J, Sobotka-Plojhar M, Exalto N, van Geijn HP. A connective tissue membrane in the right atrium (Chiari's network) as a cause of fetal cardiac arrhythmia. Am J Obstet Gynecol. 1982;142(6 Pt 1):709–712. doi: 10.1016/s0002-9378(16)32448-6.
  12. Wolfe BL, Stephens EH, Tannous P, Kalinowski V, Lay AS, Forbess JM, Ramlogan SR. Obstructing Eustachian valve in a newborn presenting with profound hypoxemia and atrial arrhythmias. JTCVS Tech. 2020;3:265–266. doi: 10.1016/j.xjtc.2020.04.008.
  13. Gad A, Mannan J, Chhabra M, Zhang XX, Narula P, Hoang D. Prominent Eustachian Valve in Newborns: A Report of Four Cases. AJP Rep. 2016;6(1):e33–e37. doi: 10.1055/s0035-1565920.

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Copyright (c) 2021 Tarayan M.V., Drozdova A.I., Bondareva I.O., Efremov E.S., Vishnyakova M.V.

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