Etiology |
Sporadic defect in body lateralization around day 28 of gestation |
Sporadic defect in body lateralization around day 28 of gestation |
Incidence |
Between 1:10,000 and 1:20,000 |
Between 1:10,000 and 1:20,000 |
Gender ratio |
2:1 female ratio |
2:1 male ratio |
Age predilection |
Congenital aberration seen at birth, but may be diagnosed in infancy or later in life depending on patient’s need for imaging |
Congenital aberration seen at birth, but may be diagnosed in infancy or later in life depending on patient’s need for imaging |
Risk factors |
No known risk factors |
No known risk factors |
Treatment |
None if patient truly has isolated levocardia. Surgery if cyanotic heart lesion present |
None if patient truly has isolated levocardia. Surgery if cyanotic heart lesion present; vaccination if anatomically asplenic |
Prognosis |
Often comorbid with CHD (50–90%), which, if severe, may cause death at a young age. Prognosis is good if heart lesion not present or is repaired. |
Often comorbid with CHD (nearly 100%), which, if severe, may cause death at a young age. Prognosis otherwise guarded due to risk of overwhelming sepsis. |
Findings on imaging |
Discordant position of cardiac situs relative to abdominal viscera. Stomach often on right side, with one or more spleens. Intestine may be mal- or non-rotated. Liver is often bridging with midline gallbladder. IVC interruption with azygos or hemiazygos continuation. Bilateral bilobed lungs with hyparterial bronchi. |
Discordant position of cardiac situs relative to abdominal viscera. Stomach often on right side, with no spleen present. Intestine may be mal- or non-rotated. Liver is often bridging with midline gallbladder. IVC ipsilateral to aorta. Bilateral trilobed lungs with eparterial bronchi. |