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

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.

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Publication Details

Journal
Cureus
Published
2026-02-12
DOI
https://doi.org/10.7759/cureus.103485
Primary Topic
Congenital Diaphragmatic Hernia Studies
Type
article
Field-Weighted Citation Impact
0.00
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article

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

Shawn Singh, Sarika Gupta, Himanshu Gupta
Cureus
Congenital Diaphragmatic Hernia Studies
article

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

Shawn Singh, Sarika Gupta, Himanshu Gupta
article en

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.

CureusVol. 18(2)
King George's Medical University (IN)
Good health and well-being
Openalex Percentile: Top 59%
Congenital Diaphragmatic Hernia Studies
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