New MRI Findings in Fukuyama Congenital Muscular Dystrophy: Brain Stem and Venous System Anomalies

A Hirasawa-Inoue1, N Sato2, Y Shigemoto3

  • 1From the Departments of Child Neurology (A.H.-I., A.I., E.T., H.K., M.S.).

Abstract

Insights

Fukuyama congenital muscular dystrophy shows characteristic brain stem abnormalities and venous system issues on MRI, including a high risk of hemorrhage. These findings aid in diagnosing this rare genetic disorder.

Area of Science:

  • Neurology
  • Radiology
  • Medical Imaging

Background:

  • Fukuyama congenital muscular dystrophy (FCMD) is associated with brain stem and cerebral abnormalities.
  • Previous radiologic assessments of the brain stem and venous system in FCMD were insufficient.
  • The role of the cerebral venous system in FCMD anomaly development warrants further investigation.

Purpose of the Study:

  • To evaluate brain stem and cerebral venous system findings on MR imaging in patients with FCMD.
  • To identify potential radiologic markers for diagnosing FCMD.

Main Methods:

  • Retrospective review of MR imaging in 27 FCMD patients.
  • Visual assessment of brain stem structures and signal intensity using T2WI, FLAIR, and DIR.
  • Evaluation of cerebral, superficial, and deep veins using T2WI and SWI, with and without hemorrhage.

Main Results:

  • Brain stem 'fluffy structures' observed in 96.3% of cases on T2WI.
  • Superficial high signal intensity noted in 96.3% (T2WI) and 92.6% (FLAIR).
  • Venous system abnormalities included superficial cerebral vein hypoplasia (100%), dilated/tortuous subependymal veins (40.0% on SWI), and hemorrhage (60.0% on SWI).

Conclusions:

  • Brain stem structural and signal abnormalities are valuable MR imaging findings for FCMD diagnosis.
  • Venous system abnormalities are significant in FCMD.
  • FCMD patients have a high risk of hemorrhage, requiring clinical awareness.

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