Atrial septal defect with pulmonary hypertension

Case contributed by randers

Presentation

34-year-old male who presents with vomiting and history of peptic ulcer disease. His past medical history is also significant for syncope and hypertrophic cardiomyopathy diagnosed in 2010.

Patient Data

Age: 34
Gender: Male
Modality: X-ray

PA view of chest reveals bilaterally enlarged pulmonary arteries. Lateral chest radiograph displays marked enlargement of the pulmonary arteries.

Modality: X-ray

Lateral chest radiograph displays marked enlargement of the pulmonary arteries measuring up to 4.7 cm.

Modality: Ultrasound

Echocardiogram demonstrates a patent atrial septal defect (ASD) measuring 2.7 cm with right ventricular hypertrophy with wall thickness of 11 mm (>5 mm).

Case Discussion

We present a case of a 34-year-old male who presents with tooth pain and inability to take anything PO with past medical history significant for syncope and hypertrophic cardiomyopathy diagnosed in 2010.  He was diagnosed with an atrial septal defect measuring 2.7 cm. 

Embryological development of the heart begins during week five of gestational development of the fetus.  There are various types of ASD determined by the defect during embryo development.  The physiologic picture of ASD will determine the clinical progression of the patient.  The high pressure system of the left side of the heart causes blood to flow through the ASD into the right atrium during atrial systole (left to right shunt, non-cyanotic).  Gradually, the excess blood volume will cause tension on the pulmonary artery resulting in pulmonary vascular injury and hypertrophy to compensate.  As pressure within the right heart continues to increase, blood within the heart will begin to shunt from right to left (cyanotic).  The oxygen saturation of our patient at the time of presentation was 94%, confirming that he remains non-cyanotic.  Eisenmenger syndrome is a complication of ASD and is established when the patient develops cyanosis and pulmonary arterial disease as a result of communication between the systemic and pulmonary systems.

Right ventricular hypertrophy is defined on echo by wall thickness greater than 5 mm.  If the mean pulmonary artery pressure exceeds 25 mm Hg at rest, the patient is considered to have pulmonary hypertension.  In our patient, echo reveals severe pulmonary hypertension is noted with Right Ventricular Systolic Pressure is calculated at 120 mmHg. When an ASD is diagnosed, about 10% of patients will have existing pulmonary hypertension.

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Case Information

rID: 48742
Diagnostic certainty: Certain
Case created: 21st Oct 2016
Last edited: 1st Dec 2016
Systems: Cardiac, Chest
Inclusion in quiz mode: Included

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