Ebstein's anomaly of the tricuspid valve

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Ebstein's anomaly of the tricuspid valve
Chest X-ray of a patient with Ebstein's anomaly
Image courtesy of RadsWiki
ICD-10 Q22.5
ICD-9 746.2
OMIM 224700
DiseasesDB 4039
eMedicine med/627 
MeSH D004437

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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] and Claudia P. Hochberg, M.D. [2]

Associate Editor-In-Chief: Cafer Zorkun, M.D., Ph.D. [3]

Please Join in Editing This Page and Apply to be an Editor-In-Chief for this topic: There can be one or more than one Editor-In-Chief. You may also apply to be an Associate Editor-In-Chief of one of the subtopics below. Please mail us [4] to indicate your interest in serving either as an Editor-In-Chief of the entire topic or as an Associate Editor-In-Chief for a subtopic. Please be sure to attach your CV and or biographical sketch.

Overview

Ebstein's anomaly is a congenital heart defect in which the opening of the tricuspid valve is displaced towards the apex of the right ventricle of the heart (congenital apical displacement of the tricuspid valve that typically causes significant tricuspid regurgitation).

The annulus of the valve is in normal position. The valve leaflets however, are to a varying degree attached to the walls and septum of the right ventricle. There is subsequent atrialization of a portion of the morphologic right ventricle (which is then contiguous with the right atrium). This causes the right atrium to be large and the anatomic right ventricle to be small in size. 50% of cases involve an atrial shunt (either a PFO or an ASD).

Etymology

Ebstein's anomaly was named after Wilhelm Ebstein.[1][2]

Diagnoses Ebstein's Anomaly of the Tricuspid Valve should be Distinguished from

Associated Abnormalities

While Ebstein's anomaly is defined as the congenital displacement of the tricuspid valve towards the apex of the right ventricle, it is often associated with other abnormalities.

Anatomy

Typically, there are anatomic abnormalities of the tricuspid valve, with enlargement of the anterosuperior leaflet of the valve which is often adherent to the right ventricular free wall.

About 50% of individuals with Ebstein's anomaly have an associated shunt between the right and left atriums, either an atrial septal defect ASD or a patent foramen ovale PFO.

- The tricuspid valve leaflets are displaced toward the RV apex.

- The RV cavity is dilated and the free wall is thin.

- May be associated with LV dysfunction and mitral valve prolapse (MVP).

- It has also been associated with pulmonic stenosis (PS), VSD, pulmonary hypertension, bicuspid aortic valve and right sided aortic arch.

-It is commonly associated with congenitally corrected transposition of the great vessels and occasionally with tetralogy of Fallot.

- Is often associated with one or more accessory conduction pathways in 25%, and WPW in 13%. Usually this is a right sided accessory pathway.

- The presence of an ASD permits right-to-left shunting and cyanosis. The degree of cyanosis is related to the degree of tricuspid regurgitation (TR), tricuspid stenosis (TS) and the compliance of the RV.

Epidemiology and demographics

  • Is a rare congenital heart disease.
  • About 1:1,000 patients with congenital heart disease, or 1:210,000 live births.
  • Males = females.
  • Higher incidence in infants whose mothers are treated with Lithium Carbonate during pregnancy

Genetics

  • Multifactorial inheritance, risk if a sibling has the disease is 1%.

Diagnosis

History | Physical examination | Laboratory findings | CT and MRI

Treatment

Prognosis

References

  1. Template:WhoNamedIt
  2. W. Ebstein. Über einen sehr seltenen Fall von Insufficienz der Valvula tricuspidalis, bedingt durch eine angeborene hochgradige Missbildung derselben. Archiv für Anatomie, Physiologie und wissenschaftliche Medicin, Leipzig, 1866, 238-254.

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