Hirayama Disease in A Patient with Loeys-Dietz Syndrome: The First Reported Association.

Authors

Lorenzo Silva-Hernández, Borja Cabal-Paz, Pablo Tutor de Ureta, Beatriz Brea-Álvarez, Beatriz de la Puente-Garrido

Published in

European journal of case reports in internal medicine. Volume 13. Issue 10. Pages 007397. Epub Sep 25, 2026.

Abstract

Hirayama disease (HD) is a rare, self-limiting cervical flexion myelopathy causing progressive, painless distal upper-limb weakness, typically in young Asian males. Loeys-Dietz syndrome (LDS) is a heritable connective tissue disorder due to TGF-β pathway variants, associated with dural ectasia. Their co-occurrence has not previously been reported.
We describe a 23-year-old woman with genetically confirmed LDS type 2 who developed progressive, painless distal upper-limb weakness, initially unilateral and later bilateral. Examination and electrophysiology showed a C7-T1 polyradicular pattern. Dynamic flexion cervical magnetic resonance imaging (MRI) demonstrated anterior displacement of the posterior dural sac at C5-C7, fully reversible on extension, confirming HD.
This presentation was atypical for HD (female sex, third-decade onset, bilateral course), yet electrophysiological and dynamic-MRI findings were unequivocal. HD should be considered in patients with heritable connective tissue disease presenting with progressive distal upper-limb weakness, irrespective of sex or age, and dynamic flexion MRI is essential for diagnosis.
Hirayama disease should be considered in progressive, painless distal upper-limb weakness even outside its classic demographic (young Asian males), including in women and in patients with an underlying connective tissue disorder.Dynamic (flexion) cervical magnetic resonance imaging is required to demonstrate the anterior dural sac displacement that confirms the diagnosis and avoids unnecessary immunomodulatory treatment.Heritable connective tissue disorders such as Loeys-Dietz syndrome may modify cervical dural biomechanics, and internists should be aware of neuromuscular complications beyond the classical cardiovascular, skeletal and dural manifestations.

PMID:
42877828
Bibliographic data and abstract were imported from PubMed on 16 Oct 2026.

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