Clinical question
27-year-old women with irritable bowel syndrome.
- Multiple masses found in abdominal CT
- Interpreted as Neurofibromatosis
- Referred to Johns Hopkins Neurofirbomatosis clinic for further evaluation
- Clinically found to have hand weakness bilaterally
- EMG showed diffuse abnormality suggesting hereditary neuropathy or CIDP
- Referred for Brachial Plexus MR Neurography for further evaluation
Clinical images
Interpretation
- Diffusely enlarged and hyperintense bilateral brachial plexus segments
- Symmetrical involvement
- No abnormal enhancement
- DTI - Symmetrically low FA values (0.2) and high ADC values - 1.9 and 2.0. Tractography shows mildly disrupted tracts
- Diagnosis - Charcot Mary Tooth Disease (CMT)
Consequences for treatment
- MR Neurography provided initial diagnosis for abnormality
- MR Neurography served as pre-intervention road map for biopsy
- Final diagnosis - CMT type 1A
- The diagnosis was proven from subsequent genetic testing and surgical biopsy of a intercostal lesion