- Department of Rehabilitation Medicine, Singapore General Hospital, Singapore
- Department of General Medicine, Sengkang General Hospital, Singapore.
Yeow Leng Tan, Department of Rehabilitation Medicine, Singapore General Hospital, Singapore.
DOI:10.25259/SNI_677_2021Copyright: © 2021 Surgical Neurology International This is an open-access article distributed under the terms of the Creative Commons Attribution-Non Commercial-Share Alike 4.0 License, which allows others to remix, tweak, and build upon the work non-commercially, as long as the author is credited and the new creations are licensed under the identical terms.
How to cite this article: Yeow Leng Tan1, Minghe Moses Koh2. Cervical neuromyelitis optica with thoracic ependymoma. 09-Aug-2021;12:396
How to cite this URL: Yeow Leng Tan1, Minghe Moses Koh2. Cervical neuromyelitis optica with thoracic ependymoma. 09-Aug-2021;12:396. Available from: https://surgicalneurologyint.com/surgicalint-articles/11032/
Background: The occurrence of cervical neuromyelitis optica (NMO) in a patient with a thoracic ependymoma is uncommon. Here, we present a patient with a spinal ependymoma who developed the new onset of NMO 2 months later.
Case Description: A 66-year-old male presented with right lower limb weakness. The magnetic resonance (MR) revealed an intramedullary spinal cord tumor at the T2-T4 level. It was surgically excised and proved pathologically to be an ependymoma. 2 months later, the patient presented with an acute partial quadriparesis and a high signal intensity cord lesion at the C2-C3 level attributed to seropositive NMO (i.e. additional diagnostic studies confirmed this diagnosis).
Conclusion: Patients with intramedullary thoracic ependymomas may also develop NMO resulting in recurrent/ new neurological deficits. Critical studies utilized to diagnose NMO include brain and spine MRs showing unique intramedullary brain/cord lesions, aquaporin-4 positive serology, and classical abnormal visual studies. If the diagnosis of NMO is established, multiple additional medical therapies are warranted.
Keywords: Aquaporin-4 antibodies, Ependymoma, Neuromyelitis optica, Rehabilitation, Spine
Ependymoma is a frequent condition seen in the neurosurgical unit. However, the occurrence of cervical neuromyelitis optica (NMO) with a thoracic ependymoma in a single patient is not commonly encountered in the clinical setting. Here, we present a patient with a spinal ependymoma who developed the new onset of NMO 2 months later.
A 66-year-old male presented with right lower limb paresis. The urgent magnetic resonance (MR) revealed a T2 to T4 intramedullary lesion that enhanced with contrast consistent with the diagnosis of an ependymoma. Following a T3 to T4 laminectomy, this diagnosis ependymoma was confirmed [
However, 2 months later, he was readmitted with the acute onset of left palm numbness, left lower limb paresis, and urinary frequency (i.e. partial quadriparesis). The repeat neuroaxis MR imaging (MRI) studies documented a new C2-C3 intramedullary his signal lesion [
Magnetic resonance imaging sagittal T2 image of the cervical and thoracic spine in August 2019 revealing new intramedullary enhancement over the cervical C2-3 region before treatment with steroids and immunosuppressive agents. See red arrow. The blue arrow indicates the post-surgical excision site for the thoracic ependymoma.
Despite immediate medical treatment with steroid and immunosuppression, the motor and sensory recovery remained incomplete [
Here, we presented a patient who originally presented with a paraparesis attributed to a T2-T4 thoracic ependymoma, who 2 and 18 months later developed acute quadriparesis due to NMO (C2-C3, and C2- 7, respectively). The diagnosis of NMO utilizing brain/holo spinal MR and positive AQP4 serology was clearly established, thus avoiding the need for an intramedullary cervical cord biopsy (i.e., to rule out metastatic ependymoma)and its inherent risks.[
Classical laboratory and MR findings NMO
Classical NMO-immunoglobulin G (IgG) tests and c MR findings of NMO helped confirm this diagnosis in this patient, ruling out metastatic ependymoma. NMO-IgG acts against the AQP-4 water channels which are highly populated in the astrocytes for water transportation across the cell membrane, and NMO on brain/spinal MRI imaging, are typically hyper-intense on T2-weighted studies with lesions distributed to the peri-ependymal regions.[
It is unusual for a patient to present with paraparesis due to an intramedullary thoracic ependymoma (T2-T4) followed by the diagnosis of NMO. As these two entities may mimic each other, it is important to differentiate between the two utilizing MRI brain/spine imaging, AQP4 serology, and visual tests.
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