Magnetization Transfer MRI measurements of Cervical Spinal Cord abnormalities in patients with Neuromyelitis Optica
نویسندگان
چکیده
Objective: Neuromyelitis optica (NMO) is an inflammatory and demyelinating disease of central nervous system that preferentially affects the optic nerve and spinal cord. NMO has long been thought of as a rare and severe variant of multiple sclerosis (MS), however, clinical, immunological and pathological characteristics that distinguish it from MS are now recognized [1]. As NMO involves recurrent and aggressive attacks of blindness and paralysis, unlike the attacks in MS, it is crucial to diagnose NMO in the early stages in order to especially provide the proper treatment [2]. However, current diagnostic criteria in routine practice using conventional T1(T1w) and T2-weighted (T2w) images are not sensitive to early degenerative changes in NMO. Recent studies using diffusion tensor imaging have shown abnormality in normal appearing tissues of brain and spinal cord [3,4]. However, normal appearing tissue damage in cervical spinal cord has not been widely investigated due to technical limitations although understanding pathological mechanism in the cervical spinal cord is crucial in research of NMO. The goal of this research is to apply magnetization transfer-weighted (MTw) imaging for assessing the pathological mechanism of normal appearing cervical spinal cord tissue damage in patients with NMO.
منابع مشابه
Imaging Surrogates of Disease Activity in Neuromyelitis Optica Allow Distinction from Multiple Sclerosis
Inflammatory demyelinating lesions of the central nervous system are a common feature of both neuromyelitis optica and multiple sclerosis. Despite this similarity, it is evident clinically that the accumulation of disability in patients with neuromyelitis optica is relapse related and that a progressive phase is very uncommon. This poses the question whether there is any pathological evidence o...
متن کاملParoxysmal Chorea as a Relapse of Myelopathy in a Patient with Neuromyelitis Optica
Movement disorders secondary to intrinsic spinal cord disease are rare. Paroxysmal chorea has not yet been reported in the neuromyelitis optica (NMO). We report a 43-year-old woman with relapsing-remitting cervical myelopathy who developed paroxysmal chorea during clinical exacerbation of NMO. MRI scan of the cervical spine revealed a long segmental enhancing lesion, but brain MRI did not show ...
متن کاملO 11: Diagnosis and Management of Neuromyelitis Optica
Typical NMO is characterized by simultaneous or sequential acute transverse myelitis and optic neuritis. Spinal cord lesions extending over 3 or more vertebral segments and normal brain imaging are the typical MRI findings in NMO. In typical cases with positive NMO antibody the diagnosis is easy but in seronegative and atypical cases with different clinical manifestations and MRI features the d...
متن کاملSeropositive Neuromyelitis Optica imitating an Intramedullary Cervical Spinal Cord Tumor: Case Report and Brief Review of the Literature
A 44-year-old woman with progressive cervical myelopathy and central cord syndrome was noted to have an extensive cervical intramedullary contrast-enhancing lesion on magnetic resonance imaging (MRI). The lesion resembled a spinal astrocytoma or ependymoma that required surgical intervention. She was subsequently diagnosed to have neuromyelitis optica (NMO), a rare idiopathic inflammatory demye...
متن کاملTeaching neuroimages: neuromyelitis optica misdiagnosed as spinal cord tumor.
A 17-year-old girl presented with acute-onset cervical pain, followed by left arm weakness and gait disturbances. Spinal cord astrocytoma was diagnosed by MRI performed at an outpatient facility (figure, A and B). The patient was admitted to the neurosurgery department to undergo spinal cord biopsy. A second neurologic evaluation indicated neuromyelitis optica (NMO) as the most likely diagnosis...
متن کامل