# Swyer-James-MacLeod Syndrome: A Rare Cause of Unilateral Hyperlucent Lung in a Two-Year-Old Male Child

**Authors:** Sarika Gupta, Himanshu Gupta, Sakshi Singh

PMC · DOI: 10.7759/cureus.103485 · Cureus · 2026-02-12

## TL;DR

A two-year-old boy was diagnosed with a rare lung condition called Swyer-James-MacLeod syndrome, which is usually found in older children.

## Contribution

This case highlights the importance of considering SJMS in young children with unexplained lung issues.

## Key findings

- SJMS was diagnosed in a two-year-old with recurrent lung infections using imaging techniques.
- Early diagnosis in young children is rare but possible with characteristic radiologic findings.
- Multimodal imaging is crucial for identifying SJMS in early childhood.

## Abstract

Swyer-James-MacLeod syndrome (SJMS) is an uncommon post-infectious bronchiolitis obliterans-related pulmonary disorder characterized by a unilateral hyperlucent lung with associated hypovascularity on chest radiography and CT, and markedly reduced perfusion on ventilation-perfusion scintigraphy. Although typically identified in older children or adolescents due to its insidious progression, diagnosis in early childhood remains rare and diagnostically challenging.

This report describes a two-year-old male child with recurrent lower respiratory tract infections who was ultimately diagnosed with SJMS based on characteristic radiologic hallmarks. This case emphasizes the importance of maintaining a high index of suspicion for SJMS in young children presenting with persistent or unexplained unilateral pulmonary abnormalities. It highlights the critical role of multimodal imaging in early recognition.

## Linked entities

- **Diseases:** Swyer-James-MacLeod syndrome (MONDO:0800120)

## Full-text entities

- **Diseases:** SJMS (MESH:D019568), pulmonary disorder (MESH:D008171), respiratory tract infections (MESH:D012141), bronchiolitis obliterans (MESH:D001989)

## Full text

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## Figures

6 figures with captions in the complete paper: https://tomesphere.com/paper/PMC12988829/full.md

## References

8 references — full list in the complete paper: https://tomesphere.com/paper/PMC12988829/full.md

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Source: https://tomesphere.com/paper/PMC12988829