CASE A
A 24-year-old woman with a history of neurofibromatosis type 1 presenting with a 3-month history of weakness and tremors in her right hand. Ax , axial; Cor , coronal; Sag , sagittal.

CASE B
A 17-year-old male with foot deformity and scoliosis. Ax , axial.

CASE C
A 59-year-old man presenting with pain and sensation of a mass in the right side of the neck. Ax , axial; Cor , coronal; Sag , sagittal.

CASE D
A 35-year-old woman presenting with 2 weeks of increasing dull pain in the right upper quadrant. Ax , axial; Cor , coronal.

CASE E
A 24-year-old presenting with a 2-week history of bilateral lower extremity weakness. Ax , axial; Sag , sagittal.

DESCRIPTION OF FINDINGS

  • Case A: Bilateral, enhancing, plexiform, mass-like enlargement of the cervical nerve roots extending into the extraforaminal paraspinal region.

  • Case B: Enhancement and diffuse enlargement of the sacral foraminal nerve roots and extraforaminal sacral nerves bilaterally.

  • Case C: An extramedullary mass expanding the right C2-C3 neural foramen. The mass has a target appearance with central hypointensity on T2-weighted images.

  • Case D: A heterogeneously enhancing large right upper quadrant mass extends out of the spinal canal through a right upper lumbar neural foramen.

  • Case E: Diffuse enhancement of the cauda equina nerve roots and pia of the conus medullaris.

Diagnosis

Case A

Plexiform neurofibromas in the setting of neurofibromatosis type 1 (NF1)

Case B

Charcot-Marie-Tooth (CMT) disease

Case C

Solitary benign peripheral nerve sheath tumor confirmed by biopsy

Case D

Malignant peripheral nerve sheath tumor confirmed by excisional biopsy

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