# Atypical presentation of unilateral pulmonary artery agenesis diagnosed postpartum

## TL;DR

A 27-year-old woman was diagnosed with a rare birth defect in her pulmonary artery after childbirth, showing how this condition can present unexpectedly in adults.

## Contribution

This case report adds to the understanding of UAPA's atypical presentation in adults, particularly during the postpartum period.

## Key findings

- UAPA was diagnosed in a postpartum woman with symptoms resembling pregnancy complications.
- The case emphasizes the challenges of diagnosing UAPA during the postpartum period.
- Early diagnosis is crucial for better pregnancy outcomes in UAPA patients.

## Abstract

A 27-year-old woman developed a cough, shortness of breath, and symptoms mimicking pregnancy complications 6 days after childbirth. Unilateral pulmonary artery agenesis (UAPA), a rare congenital condition, was diagnosed through a chest CT scan. This case highlights the variable presentation of UAPA, even in adults, and the challenges of diagnosis during the postpartum period. Early diagnosis and management are critical for improving pregnancy outcomes in women with UAPA.