Tumefactive multiple sclerosis versus high grade glioma: A diagnostic dilemma

Author:

French Heath1,Fontes-Villalba Ariadna2,Maharaj Monish3,Naidoo Catherine Soo Yee4,Bhatia Kartik5,Paterson Amanda6,Cook Raymond1,Parratt John2

Affiliation:

1. Departments of Neurosurgery, Royal North Shore Hospital, St. Leonards, New South Wales, Australia,

2. Neurology, Royal North Shore Hospital, St. Leonards, New South Wales, Australia,

3. Department of Neurosurgery, Waikato Hospital, Hamilton, New Zealand,

4. Department of Radiology, Royal North Shore Hospital, St. Leonards, New South Wales, Australia,

5. Department of Radiology, Children’s Hospital, Westmead,

6. Department of Neurosurgery, John Hunter Hospital, New Lambton Heights, New South Wales, Australia.

Abstract

Background: Tumefactive demyelinating lesions (TDL) share similar clinical features and magnetic resonance imaging (MRI) characteristics with high grade glioma (HGG). This study develops an approach to navigating this diagnostic dilemma, with significant treatment implications as the management of both entities is drastically different. Methods: A retrospective analysis of 41 TDLs and 91 HGG with respect to demographics, presentation and classical MRI characteristics was performed. A diagnostic pathway was then developed to help diagnose TDLs based on whole neuraxis MRI and cerebrospinal fluid (CSF) examination. Results: The diagnosis of TDL is more likely than HGG in younger females who present with subacute or chronic symptoms. MRI characteristics favoring TDL over HGG include smaller size, open rim enhancement, little or no associated edema or mass effect and the presence of a T2 hypointense rim. MRI of the whole neuraxis for detection of other lesions typical of multiple sclerosis (MS), in combination with a lumbar puncture (LP) showing positive CSF-specific oligoclonal bands (OCB), was positive in 90% of the TDL cohort. Conclusion: The diagnostic pathway, proposed on the basis of specific clinicoradiological features, should be followed in patients with suspected TDL. If MRI demonstrates other lesions typical of MS and LP demonstrates positive CSF-specific OCBs, then patients should undergo a short course of IV steroids to look for clinical improvement. Patients, who continue to deteriorate, do not demonstrate other lesions on MRI or where the LP is negative for CSF-specific OCB, should be considered for biopsy if safe to do so. This pathway will give the patients the best chance at neurological preservation.

Publisher

Scientific Scholar

Subject

Neurology (clinical),Surgery

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