scholarly journals CT and MRI imaging of the brain in MELAS syndrome

2013 ◽  
Vol 78 (3) ◽  
pp. 61-65 ◽  
Author(s):  
Anna Walecka
Keyword(s):  
Melas Syndrome ◽  
Mri Imaging ◽  
The Brain ◽  
Ct And Mri

CT and MRI imaging of glomus tumors of the temporal bone

2018 ◽  
pp. 26-32
Author(s):  
E. A. Stepanova ◽  
М. V. Vishnyakova ◽  
V. I. Sambulov ◽  
I. Т. Mukhamedov
Keyword(s):  
Magnetic Resonance ◽  
Diagnostic Imaging ◽  
Temporal Bone ◽  
Glomus Tumor ◽  
Magnetic Resonance Tomography ◽  
Mri Imaging ◽  
Glomus Tumors ◽  
Magnetic Resonance Imaging Mri ◽  
Temporal Bone Tumor ◽  
Ct And Mri

Glomus tumor is one of the most common temporal bone tumors. Most of them are benign and locally invasive, some are occasionally able to metastasize and have signs of malignancy. Diagnostic imaging is necessary before treatment. Computer tomography (CT) is traditionally used as a primary method of diagnosis, to recognize changes in the temporal bone. Role of magnetic resonance imaging (MRI) in temporal bone tumor diagnosis is not definitively determined.Purpose. To assess the possibilities of computer and magnetic resonance tomography, to develop an algorithm for the application of diagnostic imaging methods in the diagnosis of glomus tumors of the temporal bone.Material and methods. The article presents the experience of diagnosing 30 patients with glomus tumors.Results. The tympanic form of the glomus tumor was observed in 11 cases (37%), tympano-yugular in 19 cases (63%). CT and MRI data totally coincided in cases of small tumors (type A and B). In the presence of extended forms CT ability of assessing bone invasion, involvement of the internal carotid artery, internal jugular vein, and dural sinuses was lower than the MRI.

CT and MRI of the Brain in Inherited Neurometabolic Disorders

1992 ◽  
Vol 7 (1_suppl) ◽  
pp. S112-S131 ◽  
Author(s):  
Jan Brismar
Keyword(s):  
World Literature ◽  
Autosomal Recessive ◽  
Wide Spectrum ◽  
Neurometabolic Disorder ◽  
Neurometabolic Disorders ◽  
Number Of Patients ◽  
Pediatric Neurologist ◽  
The Brain ◽  
Very High ◽  
Ct And Mri

The incidence of many autosomal recessive neurometabolic disorders is very high in Saudi Arabia, probably as a result of the frequency of consanguineous marriages. Because our hospital is the main referral center for the entire Kingdom, we examine a large number of patients who have a wide spectrum of neurometabolic disorders. We add our experience and review the world literature. Though a specific diagnosis is radiologically possible in a few disorders, the diagnosis must always be verified biochemically. When the patient is referred from a pediatric neurologist with the diagnosis of neurometabolic disorder, the aim of the neuroradiologist is to determine the amount of brain damage present and to follow the response to given therapy. When the patient is referred with a nonspecific diagnosis, such as delayed development, the aim is to suggest the possibility of a neurometabolic disorder and to initiate further evaluation including possible therapy and genetic counseling. (J Child Neurol 1992;7(Suppl):S112-S131.)

Primary facial nerve paraganglioma: report and review of the literature

2020 ◽  
Vol 13 (12) ◽  
pp. e237537
Author(s):  
Jonathan Austin Berry ◽  
Cherie Ann O Nathan ◽  
Ashley B Flowers ◽  
Gauri Mankekar
Keyword(s):  
Facial Nerve ◽  
Surgical Resection ◽  
Facial Paralysis ◽  
Clinical Importance ◽  
Mri Imaging ◽  
Review Of The Literature ◽  
Surveillance Imaging ◽  
Complete Surgical Resection ◽  
History Of ◽  
Ct And Mri

This report describes the diagnosis and treatment of a patient with a rare primary facial nerve paraganglioma as well as a review of the current literature. A 60-year-old male patient presented to our clinic with a 4-month history of left-sided progressive facial paralysis House-Brackmann V. Biopsy taken during facial nerve (FN) decompression confirmed the diagnosis of paraganglioma. The left FN was sacrificed during resection of the mass and a 12-7 jump graft, using the left greater auricular nerve, was performed with acceptable outcomes. The rarity of these tumours does not discount their clinical importance or the necessity to include them in the differential when presented with unilateral FN paralysis. Investigation should begin with CT and MRI imaging to identify and localise the potential mass. Histologic confirmation requires tissue. While surveillance imaging is occasionally an option, often complete surgical resection of the mass and sacrifice of the nerve is necessary.

scholarly journals P.059 Brachial plexus enhancement in acute flaccid myelitis: A novel radiographic finding

2019 ◽  
Vol 46 (s1) ◽  
pp. S30
Author(s):  
SC Hammond ◽  
M Almomen ◽  
A Mineyko ◽  
A Pauranik
Keyword(s):  
Spinal Cord ◽  
Peripheral Nerves ◽  
Grey Matter ◽  
Pediatric Patients ◽  
Radiographic Finding ◽  
Mri Imaging ◽  
Full Spectrum ◽  
Acute Flaccid Myelitis ◽  
History Of ◽  
The Brain

Background: Acute flaccid myelitis (AFM) is a condition which causes acute paralysis in pediatric patients. Although awareness of AFM is increasing, the pathophysiology and full spectrum of clinical, biochemical, and radiographic features remain to be fully elucidated. Methods: We report a 5 year-old, previously healthy, male patient who presented with acute right upper extremity weakness following a two day history of fever, cough, and fatigue. The patient underwent extensive inflammatory and infectious workup in addition to MRI imaging of the brain, spinal cord, and bilateral brachial plexuses. Results: Infectious and inflammatory workup did not identify a causative agent. The patient was seen to have bilateral asymmetric (R>L) thickening and enhancement of the anterior horn cells of his cervical (C3-C7) spine, consistent with the spinal grey matter lesions previously described in patients with AFM. Enhancement of the corresponding anterior nerve rootlets and bilateral brachial plexuses was also seen. Conclusions: Patients with acute flaccid myelitis may demonstrate grey matter enhancement extending beyond the spinal cord to the peripheral nerves and plexuses, a radiographic finding which has not previously been published.

scholarly journals Agreement Between Computed Tomography And Magnetic Resonance Imaging In Measuring Optic Nerve Sheath Diameter

2018 ◽  
Vol 10 (3) ◽  
pp. 22
Author(s):  
Haider N. Al-Tameemi ◽  
Neda M. Helel
Keyword(s):  
Magnetic Resonance Imaging ◽  
Optic Nerve ◽  
Magnetic Resonance ◽  
Ct Scan ◽  
Optic Nerve Sheath Diameter ◽  
Resonance Imaging ◽  
Perfect Agreement ◽  
Nerve Sheath ◽  
The Brain ◽  
Ct And Mri

BACKGROUND: Neuroimaging is increasingly used as a non-invasive method to assess raised intracranial pressure (ICP). Optic nerve sheath diameter (ONSD) measurement using brain magnetic resonance imaging (MRI) has been shown to correlate well with invasively measured ICP, however little research has been conducted on the ONSD measurement using computerized tomography (CT) in correlation with ICP. This study was done to investigate whether CT scan can reliably replace MRI in measuring ONSD.METHOD: A cross-sectional comparative study was conducted on 50 adult patients (29 females and 21 males), who underwent both CT and MRI of the brain along 10-month period. Using the brain axial section, the transverse ONSD was measured at 3 mm behind the globe in both modalities. Agreement between CT and MRI readings was assessed using intraclass correlation (ICC) and Kappa method.RESULTS: There was a strongly positive and statistically significant correlation between ONSD measurement using CT scan and MRI (p value <0.001). There was almost perfect agreement between CT scan and MRI in measuring ONSD (ICC=0.987 and Kappa =0.837). Similar agreement was obtained when cases stratified into normal (≤ 5mm) and thickened (> 5mm) ONSD (ICC=0.947 and 0.972 respectively).CONCLUSION: CT scan is a reliable substitute for MRI in measuring ONSD with almost perfect agreement between the two modalities. It might be good practice to include ONSD measurement in the initial evaluation of brain CT scan in any patient with suspected raised ICP.

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