# A Case of Secondary Pulmonary Hypertension in a Patient With Atrial Septal Defect and Fetal Alcohol Syndrome

**Authors:** Maja Pirnat, Vesna Lesjak, David Šuran, Tina Lovrec Orthaber

PMC · DOI: 10.7759/cureus.65611 · 2024-07-28

## TL;DR

A man with fetal alcohol syndrome and a large heart defect developed severe lung high blood pressure, highlighting diagnostic and treatment challenges in adults with cognitive impairments.

## Contribution

Highlights the delayed diagnosis of ASD in adults with FAS and the complexities of managing secondary pulmonary hypertension.

## Key findings

- A 34-year-old man with fetal alcohol syndrome was diagnosed with severe pulmonary hypertension due to a large atrial septal defect.
- The case illustrates diagnostic delays in patients with cognitive impairments.
- Treating pulmonary hypertension in such cases poses a therapeutic dilemma due to risks of shunt closure.

## Abstract

We report a case of a 34-year-old man with fetal alcohol syndrome (FAS) presenting with dyspnea, cough, and hoarse voice. The patient was found to have severe pulmonary hypertension secondary to a large atrial septal defect (ASD). In this article, we discuss the challenges patients with FAS and other patients with cognitive impairments face that could explain the first diagnosis of such a large cardiac birth defect being made in the patient’s adulthood. Moreover, severe pulmonary hypertension due to ASD also presents a therapeutic dilemma, as shunt closure can lead to a worsening of the condition.

## Linked entities

- **Diseases:** fetal alcohol syndrome (MONDO:0000408), pulmonary hypertension (MONDO:0005149), atrial septal defect (MONDO:0006664)

## Full-text entities

- **Diseases:** hoarse voice (MESH:D006685), Pulmonary Hypertension (MESH:D006976), cognitive impairments (MESH:D003072), cardiac birth defect (MESH:D006331), cough (MESH:D003371), dyspnea (MESH:D004417), FAS (MESH:D063647), ASD (MESH:D006344)
- **Species:** Homo sapiens (human, species) [taxon 9606]

## Figures

4 figures with captions in the complete paper: https://tomesphere.com/paper/PMC11357726/full.md

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Source: https://tomesphere.com/paper/PMC11357726