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Case Reports
. 2004 Mar;25(3):494-7.

Charcot-Marie-Tooth disease: extensive cranial nerve involvement on CT and MR imaging

Affiliations
Case Reports

Charcot-Marie-Tooth disease: extensive cranial nerve involvement on CT and MR imaging

Todd R Aho et al. AJNR Am J Neuroradiol. 2004 Mar.

Abstract

We report a case of genetically verified Charcot-Marie-Tooth disease in which the patient had cranial nerve symptoms. CT and MR imaging demonstrated enlargement of several cranial nerves, as well as their skull-base foramina, with faint contrast material enhancement identified.

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Figures

F<sc>ig</sc> 1.
Fig 1.
Limited family tree demonstrates the affected members of the patient’s family, with current patient marked with arrow. (Modified from reference 6).
F<sc>ig</sc> 2.
Fig 2.
A–C, Thin-section (1-mm) coronal and axial CT images of the skull base obtained with an edge-enhancing bone algorithm show enlargement (arrows) of the mastoid canals of cranial nerve VII (A), the foramina of ovale (B), and rotundum (C) bilaterally.
F<sc>ig</sc> 3.
Fig 3.
Thin-section (2.5-mm) axial T1-weighted spoiled gradient-echo gadolinium-enhanced images of the brain obtained at 1.5 T for Gamma knife localization (trigeminal neuralgia). Cranial nerve enlargement (arrows) is most pronounced involving the mastoid or descending segments of cranial nerve VII (A), cisternal segments of cranial nerve III (B), V3 (C), and V2 (D) segments. Faint enhancement is identified.

References

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