106H Anomalous Origin of Left Pulmonary Artery from Aorta
32 year old female
dyspnea since a child
hx of Swyer James syndrome
absent perfusion to her RUL
20 years ago diagnosed with PAH on cardiac catheterization.
Rx oral therapies which a
controlled her symptoms.
CXR
CXR shows cardiomegaly, with enlarged main pulmonary artery and enlarged bilateral enlarged pulmonary arteries.
The right upper lung field is lucent consistent with the patients known Swyer James Syndrome
Additionally, the right and left hilum are prominent, which again may be secondary to pulmonary hypertension
Left Ventricular Hypertrophy
Echo
The left atrium is severely enlarged.
RV systolic function
mild RV dysfunction.
RV wall thickness is
increased (8 mm).
Mild ventricular septal flattenning
mild to moderate tricuspid regurgitation.
estimated PA pressure of
~105/45 mmHg.
Mild to moderate pulmonic valvular regurgitation.
inferior vena cava is < 2.1 cm and exhibits reduced respiratory
variability consistent with a
right atrial pressure of ~ 8 mm Hg.
consistent with severe pulmonary hypertension.
Chest CT showed
possible PDA
physical exam not consistent
no differential cyanosis,
no erythrocytosis and
normal LV dimensions.
? additional shunting
Aorta to LPA
LAE
Enlarged MPA and Pulmonary Hypertension
RAE and LVE
Right Aortic Arch
PDA Aorta to Right Pulmonary Artery
? PDA Aorta to Right Pulmonary Artery
Swyer James
Hyperlucent Anterior Segment of the RUL
Do you see a bull made of the soft tissues looking at the lucent lung?
Keep your eye on the eye of the bull as it will get progressively smaller as the bull goes to sleep and the airway narrows
AP Ventilation View NM Shows Non Ventilation of the Right Upper Lung Field and Absent Ventilation of the Left Lung
Perfusion Scan – No Perfusion of the Left Lung
Anomalous origin of the right or left pulmonary artery
from the aorta
rare prevalence of 0.33%
30% mortality rate within the first 3 months after birth (
Anomalous origin of the right pulmonary artery
most common subtype,
accounting for more than 80% o
>70% of patients with anomalous origin of the right pulmonary artery also have a
PDA,
anomalous origin of the left pulmonary artery
less commonly associated with PDA
first description by Fraentzel in
1868
proximal subtype has been reported to be
secondary to the disappearance of the fifth and sixth arches on the left,
distal subtype occurs with a persistent
fifth and absent sixth aortic arch
PDA and
atrial septal defect to be the most commonly associated congenital anomalies