0000000000288537

AUTHOR

Rosa Morabito

0000-0002-9136-9094

showing 8 related works from this author

DCE and DSC perfusion MRI acquisition: diagnostic accuracy during the follow-up of the primary and metastatic intra-axial brain tumors treated by Ste…

Distinguishing radiation necrosis from tumor recurrence and tumor progression is crucial for the evaluation of treatment response and treatment planning. The appearance of treatment-induced tissue necrosis on conventional Magnetic Resonance Imaging (MRI) are very similar to brain tumor recurrence and it could be difficult to differentiate the two entities during the follow-up MRI examinations. Dynamic Susceptibility Contrast-enhanced (DSC) and Dynamic Contrast-Enhanced (DCE) are the MRI perfusion techniques using an exogenous, intravascular, no diffusible gadolinium-based contrast agent. The aim of this study is to compare the diagnostic accuracy of DSC and DCE perfusion MRI in the differen…

Settore MED/37 - NeuroradiologiaDCEperfusion MRIDSC; DCE; brain tumors; perfusion MRIbrain tumorDSC
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3T Double Inversion Recovery Magnetic Resonance Imaging: diagnostic advantages in the evaluation of cortical development anomalies

2016

Abstract Purpose The aim of this work was to investigate the diagnostic value of the DIR sequence at 3T MR imaging operating in the evaluation of cortical development anomalies. Methods We studied 40 patients, with a previous diagnosis of cortical dysplasia, by FLAIR-3D, DIR, FSE T2 and MPR-GE T1 sequences at 3T MRI. Two independent observers evaluated, for each sequence and lesion, some semiological aspects (cortical thickness, cortical signal intensity, white-gray matter blurring, subcortical white matter intensity). We made also a quantitative evaluation of the cortical signal intensity in lesion site, drawing a ROI on each MRI sequences and comparing them to the correspondent normal con…

AdultMalePathologymedicine.medical_specialty030218 nuclear medicine & medical imagingWhite matter03 medical and health sciences0302 clinical medicineNuclear magnetic resonancePolimicrogyriamedicineHumansRadiology Nuclear Medicine and imagingProspective StudiesCortical dysplasia; DIR; Epilepsy; Polimicrogyria; Taylor; Tuberous sclerosisCerebral CortexDIRCortical dysplasiaEpilepsymedicine.diagnostic_testbusiness.industryTuberous sclerosisSignificant differenceReproducibility of ResultsMagnetic resonance imagingGeneral MedicineMiddle AgedCortical dysplasiamedicine.diseaseMagnetic Resonance ImagingIntensity (physics)DIR Epilepsy Cortical dysplasia Taylor Tuberous sclerosis PolimicrogyriaMalformations of Cortical DevelopmentTaylormedicine.anatomical_structureWhite matter hyperintensityFemaleDouble inversion recoverybusiness030217 neurology & neurosurgeryLesion siteEuropean Journal of Radiology
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Central nervous system involvement in late-onset Pompe disease: clues from neuroimaging and neuropsychological analysis

2018

Background and purpose Late-onset Pompe disease (LOPD) is a rare, multisystem disorder that is well established to mainly impair skeletal muscle function. Systematic studies exploring brain functions in LOPD are lacking. The aim of this study was to detect morphological and functional brain alterations as well as neuropsychological impairment in LOPD. Methods We studied 21 patients (10 male, mean age 49 ± 18.4 years) with defined diagnosis of LOPD, divided into two groups: one with pre-symptomatic hyperCKemia with no muscle weakness and the second with limb-girdle muscle weakness. All patients underwent 3T magnetic resonance imaging (MRI) to obtain morphological/angiographic evaluation as w…

AdultMalemedicine.medical_specialtyAdolescentSmoker scoreNeuropsychological Testscerebrovascular abnormalitieslate-onset Pompe diseaseYoung Adult03 medical and health sciences0302 clinical medicineAtrophyNeuroimagingInternal medicineConnectomemedicinecerebrovascular abnormalities Fazekas score functional magnetic resonance imaging late-onset Pompe disease Pompe disease Smoker score Neurology Neurology (clinical)HumansCognitive Dysfunction030212 general & internal medicineNeuropsychological assessmentAge of OnsetGray MatterAgedmedicine.diagnostic_testGlycogen Storage Disease Type IIbusiness.industryMuscle weaknessPompe diseaseMagnetic resonance imagingMiddle Agedmedicine.diseaseMagnetic Resonance Imagingfunctional magnetic resonance imagingHyperintensityFazekas scoreSuperior frontal gyrusNeurologyBrain sizeCardiologyFemaleNeurology (clinical)medicine.symptombusiness030217 neurology & neurosurgery
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Acute onset of bulbar amyotrophic lateral sclerosis after flu – look at the differential diagnosis: A case report

2018

Amyotrophic lateral sclerosis (ALS) is a neurodegenerative disorder affecting upper and lower motor neurones. It can be either familial (fALS) or sporadic (sALS). ALS is characterized by muscle weakness and atrophy that can involve the limbs and trunk (i.e. the spinal form of the disease) or speech and swallowing (i.e. the bulbar form). The aetiology of sALS remains unclear although a gene–environment interaction has been proposed as a concomitant trigger for the neurodegenerative process together with viral infections, smoking, heavy metals and pesticide exposure. Herein, we report the case of a 67-year-old woman who experienced an acute onset of bulbar ALS with an atypical clinical cours…

0301 basic medicinePathologymedicine.medical_specialtyMedicine (General)DiseaseCase Reportsacute onsetBiochemistryDiagnosis Differential03 medical and health sciences0302 clinical medicineAtrophyR5-920Swallowingsporadic amyotrophic lateral sclerosisDiagnosisdifferential diagnosisInfluenza HumanMedicineHumansAmyotrophic lateral sclerosisAgedbulbar amyotrophic lateral sclerosisbusiness.industryBiochemistry (medical)Amyotrophic Lateral SclerosisMuscle weaknessCell BiologyGeneral Medicinemedicine.diseaseTrunkInfluenza030104 developmental biologyDifferentialAcute DiseaseEtiologyFamilial amyotrophic lateral sclerosisFemaleacute onset; bulbar amyotrophic lateral sclerosis; differential diagnosis; Familial amyotrophic lateral sclerosis; sporadic amyotrophic lateral sclerosis; Acute Disease; Aged; Amyotrophic Lateral Sclerosis; Diagnosis Differential; Female; Humans; Influenza HumanDifferential diagnosismedicine.symptombusiness030217 neurology & neurosurgeryHumanJournal of International Medical Research
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A multidisciplinary approach to assess recovery of consciousness in a patient with moyamoya disease

2019

Abstract Introduction Moyamoya disease (MMD) meaning “hazy puff of smoke” in Japanese is a rare chronic cerebrovascular syndrome characterized by progressive stenosis and occlusion of the internal carotid arteries (ICAs) anterior cerebral arteries (ACAs), and middle cerebral arteries (MCAs). Methods Our moyamoya patient with severely impaired cognitive and motor functions underwent a specific motor and neuropsychological rehabilitative treatments to assess the recovery of consciousness. Results Results obtained showed an improvement of clinical and neuropsychological examination. These findings highlighted the importance of an intensive rehabilitation techniques used in the care of disorder…

AdultMalemedicine.medical_specialtyConsciousnessmedicine.medical_treatmentCerebral arteriesNeuropsychological Tests050105 experimental psychologyrehabilitation03 medical and health sciencesBehavioral Neuroscience0302 clinical medicinePhysical medicine and rehabilitationOcclusionmedicineHumans0501 psychology and cognitive sciencesCarotid StenosisCognitive DysfunctionMoyamoya diseasedisorders of consciousnessneuropsychological evaluationPersistent vegetative stateOriginal ResearchRehabilitationbusiness.industry05 social sciencesNeuropsychologyNeurological RehabilitationCognitionRecovery of Functionmedicine.diseaseStenosisTreatment OutcomeItalyMotor SkillsCerebral Arterial DiseasesMoyamoya Diseasebusiness030217 neurology & neurosurgeryBrain and Behavior
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Intracranial venous sinus thrombosis as unusual presentation of Bing-Neel syndrome: case illustration.

2017

A 42-year-old woman presented with progressive blurred vision, vertigo, and headache. MRI showed bilateral intraocular protrusion of the optic nerve head and right transverse sinus thrombosis . Low-molecular-weight heparin was administered without symptom relief. Additional MRI showed left frontoparietal arachnoid space obliteration by pathological tissue, and infiltration of the sagittal and right transverse sinuses. After Gd administration, we observed diffuse enhancement of the dura in the left cerebral hemisphere and subdural and epicranial soft-tissue infiltration . A biopsy of the extra-axial tissue was performed. Histological examination showed a neoplasm composed of large cells with…

Adultmedicine.medical_specialtyvascular disorders03 medical and health sciencesSinus Thrombosis Intracranial0302 clinical medicinemedicineHumansBing–Neel syndromebusiness.industryWaldenstrom macroglobulinemiaWaldenstrom macroglobulinemiaBrainGeneral Medicinemedicine.diseasecentral nervous systemThrombosisMagnetic Resonance ImagingIntracranial venous sinusSurgeryBing-Neel syndromeFemalePresentation (obstetrics)businessBing-Neel syndrome Waldenstrom macroglobulinemia central nervous system vascular disordersBing-Neel syndrome; Waldenstrom macroglobulinemia; central nervous system; vascular disorders030217 neurology & neurosurgery030215 immunology
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Perfusion computed tomography of intracranial meningiomas: In vivo correlation of cerebral blood volume and vascular permeability

2015

Background A noninvasive method to predict the grade of a meningioma would be desirable since it would anticipate information about tumour nature, recurrence and improve tumour management and outcomes. The aim of the present study was to assess the ability of perfusion computed tomography (PCT) technique in predicting the meningioma grade before surgery. Data from PCT, such as cerebral blood volume (CBV) and permeability surface (PS), were correlated with immunohistolopathological information. Methods Twenty-three patients with a diagnosis of intracranial meningioma underwent PCT for pre-surgical evaluation of CBV and PS. During surgery, samples from the centre and periphery of the tumour w…

Malemedicine.medical_specialtyRadiology Nuclear Medicine and ImagingneoangiogenesisNeoplastic DiseasePerfusion ImagingVascular permeabilityBlood volumePerfusion scanningCD-34; Meningioma; endoglin; neoangiogenesis; perfusion computed tomography; permeability surface-area product; Aged; Blood Volume; Capillary Permeability; Cerebrovascular Circulation; Cohort Studies; Female; Humans; Male; Meningeal Neoplasms; Meningioma; Middle Aged; Neoplasm Grading; Perfusion Imaging; Prospective Studies; Tomography X-Ray ComputedMeningiomaCapillary PermeabilityCohort StudiesmedicineMeningeal NeoplasmsHumansCD-34Prospective StudiesProspective cohort studyMeningeal NeoplasmTomographyAgedendoglinpermeability surface-area productBlood Volumebusiness.industrySettore MED/27 - NeurochirurgiaMedicine (all)General MedicineEndoglinMiddle Agedmedicine.diseaseNeoangiogenesiPeripheralX-Ray ComputedProspective StudieCerebrovascular CirculationCD-34; Endoglin; Meningioma; Neoangiogenesis; Perfusion computed tomography; Permeability surface-area product; Aged; Blood Volume; Capillary Permeability; Cerebrovascular Circulation; Cohort Studies; Female; Humans; Male; Meningeal Neoplasms; Meningioma; Middle Aged; Neoplasm Grading; Perfusion Imaging; Prospective Studies; Tomography X-Ray Computed; Neurology (clinical); Radiology Nuclear Medicine and Imaging; Medicine (all)perfusion computed tomographyFemaleRadiologyNeurology (clinical)Cohort StudieNeoplasm GradingbusinessTomography X-Ray ComputedMeningiomaPerfusionHuman
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A rare case of solitary brain Langerhans cell histiocytosis with intratumoral hemorrhage in a patient affected by Turner syndrome

2016

Background: Langerhans cell histiocytosis (LCH) is a rare disease involving clonal proliferation of cells with characteristics similar to bone marrow-derived Langerhans cells. The case of a young woman, affected by Turner syndrome and a solitary intraparenchymal LCH associated with an osteolytic lesion of the overlying skull, is presented. Case Description: The patient, with an insidious history of headache and a growing soft mass in the left frontal region, presented with a sudden generalized tonic-clonic epileptic seizure. Neuroradiological investigations showed an osteolytic lesion of the left frontal bone and an underlying brain lesion associated with recent signs of bleeding. The patie…

Pathologymedicine.medical_specialtyCase ReportHemorrhageHemorrhage Langerhans cell histiocytosis skull neoplasm03 medical and health sciences0302 clinical medicineLangerhans cell histiocytosisTurner syndromeRare caseMedicineskull neoplasmbusiness.industryPatient affectedLangerhans cell histiocytosiLangerhans cell histiocytosisSkull Neoplasmmedicine.diseaseHemorrhage; Langerhans cell histiocytosis; skull neoplasmOsteolytic lesionSkullmedicine.anatomical_structure030220 oncology & carcinogenesisSurgeryNeurology (clinical)business030217 neurology & neurosurgeryRare diseaseSurgical Neurology International
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