Thoracic spine meningioma - recurrence

Case contributed by Bruno Di Muzio
Diagnosis certain

Presentation

Late MRI surveillance after a previous benign spinal tumor resection 10 years ago. Asymptomatic.

Patient Data

Age: 37-year-old
Gender: Male

MRI Thoracic spine

mri

 

Previous T9-T11 decompressive laminectomy again identified. There is a homogeneously enhancing slightly T2 hyperintense circumscribed extradural mass occupying the left half of the spinal canal and extending through the left T9/T10 exit foramen. At the superior extreme of the mass, a tiny enhancement extends along the inferior margin of the left T 8/9 exit foramen. The component within the spinal canal has maximal axial dimensions of 14.5 x 15.5 mm and a craniocaudal extent of 29 mm.

A separate smaller enhancing lesion located anteriorly in the spinal canal immediately inferior to the main lesion measures 8 x 7 x 4 mm, and appears to be intradural.

The spinal cord is displaced into the right side of the spinal canal, with a distorted contour but no compression. There is no convincing intrinsic cord signal abnormality.

At the level of the T7 vertebral body, there is a prominent enhancing vessel applied to the left dorsal aspect of the cord, of dubious clinical significance.

No change to the enhancing T 2 hyperintense lesion within the left T10 transverse process, most likely be a hemangioma.

Small T5-6 and C6-7 left paracentral disc protrusion is and right T8/T9 paracentral disc protrusion again noted.

Conclusion: Recurrent meningioma occupying the left side of the spinal canal at T9 level with extension into the left T9/T10 and to a lesser extent T8/9 intervertebral foramina, displacing and distorting the cord without compression or intrinsic cord signal abnormality. There is a smaller anterior intradural component just below the main lesion.

 

Case Discussion

Histology: The sections show a moderately cellular meningioma. The tumor forms whorls. No sheeting arrangement is seen. The tumor cells have ovoid nuclei with no nuclear pleomorphism. There are up to 3 mitoses per 10 high power fields. No necrosis is seen. The tumor is present in the connective tissue. It is adjacent to but not invading into nerve bundles. No evidence of atypical or malignant meningioma is identified. The tumor cells are progesterone receptor negative. The topoisomerase index is 2%.

Diagnosis: Spinal tumor: Meningioma (WHO Grade I).

Spine meningiomas are slow-growing benign tumors usually resected surgically, and experiencing a recurrence index in about 10% of the cases. The main differential is made with spinal schwannomas, which can look very similar. 

 

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