From Spine to Syndrome: Incidental Spine MRI Red Flags Leading to <i>PMEPA1</i>-Related Loeys-Dietz Syndrome

A 49-year-old man with prior DeBakey IIIb dissections underwent preoperative spinal MRI for lumbar stenosis, which incidentally showed lumbosacral dural ectasia and bilateral pedicle thinning. Orthopedic review and cross-disciplinary discussion prompted reconsideration of Marfan syndrome (MFS). Under the revised Ghent criteria, the patient did not meet the diagnostic criteria despite a high systemic score (11). Targeted testing identified heterozygous PMEPA1 c.624dup, p. (Ser209Glnfs*3), supporting Loeys-Dietz syndrome with skeletally predominant features. This case illustrates that spine-MRI red flags should prompt Ghent-based re-examination and genetic referral when aortic-root features are absent, and genetic confirmation should guide cascade testing and risk-adapted surveillance of relatives.

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Publication Details

Journal
Internal Medicine
Published
2025-12-03
DOI
https://doi.org/10.2169/internalmedicine.6513-25
Primary Topic
Connective tissue disorders research
Type
article
Field-Weighted Citation Impact
0.00
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article

From Spine to Syndrome: Incidental Spine MRI Red Flags Leading to PMEPA1-Related Loeys-Dietz Syndrome

Aritaka Makino, Hidetoshi Eguchi, Masahiro Nezu
Internal Medicine
Connective tissue disorders research
article

From Spine to Syndrome: Incidental Spine MRI Red Flags Leading to PMEPA1-Related Loeys-Dietz Syndrome

Aritaka Makino, Hidetoshi Eguchi, Masahiro Nezu
article en

Abstract

A 49-year-old man with prior DeBakey IIIb dissections underwent preoperative spinal MRI for lumbar stenosis, which incidentally showed lumbosacral dural ectasia and bilateral pedicle thinning. Orthopedic review and cross-disciplinary discussion prompted reconsideration of Marfan syndrome (MFS). Under the revised Ghent criteria, the patient did not meet the diagnostic criteria despite a high systemic score (11). Targeted testing identified heterozygous PMEPA1 c.624dup, p. (Ser209Glnfs*3), supporting Loeys-Dietz syndrome with skeletally predominant features. This case illustrates that spine-MRI red flags should prompt Ghent-based re-examination and genetic referral when aortic-root features are absent, and genetic confirmation should guide cascade testing and risk-adapted surveillance of relatives.

Internal Medicine
Yamanashi Prefectural Central Hospital (JP)
Openalex Percentile: Top 60%
Connective tissue disorders research
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