A case of oligodendroglioma and multiple sclerosis: Occam's razor or Hickam's dictum?
Afsaneh ShiraniGregory F WuCaterina GianniniAnne H CrossPublished in: BMJ case reports (2018)
Tumefactive appearing lesions on brain imaging can cause a diagnostic dilemma. We report a middle-aged man who presented with right-sided optic neuritis. A brain MRI showed enhancement of the right optic nerve, and non-enhancing white matter lesions including a 3 cm right frontal lesion with adjacent gyral expansion. Cerebrospinal fluid analysis showed five oligoclonal bands not present in serum. Glatiramer acetate was started for suspected tumefactive multiple sclerosis (MS). A follow-up brain MRI 6 months later showed persistence of the frontal gyral expansion. A brain biopsy led to the diagnosis of an oligodendroglioma, isocitrate dehydrogenase-mutant and 1 p/19q co-deleted (WHO grade II), managed with surgical resection and radiotherapy. Postoperative brain MRI showed a new enhancing periventricular lesion, making the choice of optimal disease-modifying therapy for MS challenging. This case highlights the possibility of coexistence of MS and oligodendroglioma, and emphasises the importance of a tissue diagnosis when atypical MS imaging features are present.
Keyphrases
- white matter
- multiple sclerosis
- resting state
- functional connectivity
- mass spectrometry
- optic nerve
- ms ms
- high resolution
- magnetic resonance imaging
- contrast enhanced
- cerebrospinal fluid
- middle aged
- cerebral ischemia
- radiation therapy
- optical coherence tomography
- early stage
- squamous cell carcinoma
- working memory
- radiation induced