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1.
Neurol Sci ; 35(1): 15-21, 2014 Jan.
Article in English | MEDLINE | ID: mdl-24170165

ABSTRACT

Tick borne encephalitis (TBE) is an acute febrile syndrome that can be complicated with neurological symptoms ranging from mild meningitis to severe encephalomyelitis. The causative agent is a virus belonging to the family of flaviviruses. We have collected a series of 89 patients and compared the clinical course with the main data of the literature of TBE. This review in addition describes the clinical manifestations associated with TBE infections, the main molecular-biological properties of these viruses, and the different factors that define the incidence and severity of disease who are frequently situated in the age group young/adult with a social harm and functional non-negligible. This review also contains diagnostic elements and neuropathological features typical of this infection and a brief summary of vaccination against TBE.


Subject(s)
Encephalitis, Tick-Borne/complications , Nervous System Diseases/virology , Humans
2.
Neurol Sci ; 34(11): 2007-13, 2013 Nov.
Article in English | MEDLINE | ID: mdl-23636872

ABSTRACT

Rasagiline is a monoamine oxidase type-B inhibitor used as monotherapy or in addition to levodopa in the treatment of Parkinson's disease (PD). This naturalistic single-blind study was aimed at evaluating the rapidity of onset effect of rasagiline on motor symptoms in a cohort of early relatively elderly PD patients. 102 outpatients (55 males, median age 71 years) have been selected: 26 were PD therapy-naive and 76 received rasagiline as add-on therapy. The third section of the Unified Parkinson's Disease Rating Scale (UPDRSIII) and the Hoehn-Yahr (HY) scale were assessed at baseline and after 1 and 4 weeks thereafter. The mean UPDRS III total score (-6.7 at week 1 and -8.9 at week 4) and single items, as well as mean HY score (-0.40 at week 1 and -0.67 at week 4), significantly decreased from baseline (p < 0.001). Improvements were significant in both therapy-naive and add-on therapy patients: the mean decreases from baseline to week 4 in UPDRSIII and HY score were -8.8 and -0.46, and -9.0 and -0.74, respectively, in the two subgroups. The mean decrease from baseline in UPDRSIII and HY score did not significantly differ in patients aged > or ≤71 years. Rasagiline had a rapid therapeutic effect from the first week of therapy, which further improved at 4 weeks. The rapid onset of action and the absence of a dose titration are important issues in the management of the PD patient.


Subject(s)
Antiparkinson Agents/therapeutic use , Indans/therapeutic use , Monoamine Oxidase Inhibitors/therapeutic use , Parkinson Disease/drug therapy , Aged , Female , Humans , Male , Parkinson Disease/physiopathology , Single-Blind Method , Treatment Outcome
3.
Neurol Sci ; 33(3): 669-72, 2012 Jun.
Article in English | MEDLINE | ID: mdl-22057312

ABSTRACT

Tick borne encephalitis virus infection usually shows a biphasic course. In the first stage of illness symptoms are similar to a flu-like syndrome, then after a defervescence period, fever may represent with neurological manifestations ranging from mild meningitis to severe encephalomyelitis. We report the clinical case of an adult man presented with an acute proximal hyposthenia, severe hyperckemia, clinical and laboratoristic evidence of acute tick borne virus infection. This virus has a favourite tropism for the anterior horn cells of the cervical spine segment. Polio-like syndrome, usually affecting the upper limbs, is the clinical phenotype of an infection of the cervical motoneurons. Usually myelitis is associated to severe encephalitis and a complete diagnosis may be difficult in comatose patients. Rarely, an isolated polio-like syndrome may be the sole neurological complication of tick-borne encephalitis.


Subject(s)
Creatine Kinase/blood , Encephalitis, Tick-Borne/complications , Poliomyelitis/etiology , Acute Disease , Electromyography , Humans , Male , Middle Aged , Muscle, Skeletal/physiopathology , Poliomyelitis/diagnosis
4.
Neurol Sci ; 32(3): 443-7, 2011 Jun.
Article in English | MEDLINE | ID: mdl-21479612

ABSTRACT

We evaluated the efficacy of Botulinum toxin type A (BTXA) as an alternative to surgical intervention to facilitate phonation in 34 laryngectomized patients (31 males and 3 women) who were unable to produce tracheoesophageal voice because of spasm of the middle and inferior pharyngeal constrictor muscles (PCM). EMG was recorded to confirm activity in these muscles during attempted vocalization. Parapharyngeal nerve block (Carbocaine 2%, 5 cc) was used to demonstrate short-term fluent voice after relaxation of the pharyngeal constrictor muscle. At a later occasion, 100 U of Botox (Allergan) in ten patients and 50 U in two patients were injected unilaterally at one location in the PCM percutaneously under EMG guidance. All patients then underwent a voice therapy program. In 11 out of 12 patients an improvement of phonation was evident after 24-48 h and it was long lasting. This result was also seen in a patient previously myotomized without improvement. Only one patient needed to be reinjected every 3 months. At a follow-up after 3 months the EMG recorded in four patients showed a low-amplitude or complete absence of activity in the treated muscle. No side effects developed. BTX therapy, especially when associated with the speech therapy, is efficacious in restoring voice to laryngectomees who are unable to voice because of spasm of the PCMs. Our results confirm previous reports. This method is our approach of choice in managing PCM spasm because it is non-invasive, not painful, has few or no side effects, and is frequently long-lasting.


Subject(s)
Botulinum Toxins, Type A/administration & dosage , Dysphonia/drug therapy , Laryngectomy/adverse effects , Laryngectomy/rehabilitation , Phonation/drug effects , Adult , Aged , Aged, 80 and over , Botulinum Toxins, Type A/therapeutic use , Clostridium botulinum/chemistry , Dysphonia/etiology , Dysphonia/rehabilitation , Female , Humans , Male , Middle Aged , Nerve Block/methods , Neuromuscular Agents/administration & dosage , Pharyngeal Muscles/drug effects , Pharyngeal Muscles/physiopathology , Phonation/physiology , Spasm/drug therapy , Spasm/etiology , Spasm/rehabilitation , Speech, Esophageal/methods
5.
J Neurol ; 258(4): 627-33, 2011 Apr.
Article in English | MEDLINE | ID: mdl-21082324

ABSTRACT

The mechanisms underlying pain in Parkinson's disease (PD) are unclear. Although a few studies have reported that PD patients may have low pain threshold and tolerance, none could accurately assess whether there was a correlation between sensory thresholds and demographic/clinical features of PD patients. Thus, tactile threshold, pain threshold, and pain tolerance to electrical stimuli in the hands and feet were assessed in 106 parkinsonian patients (of whom 66 reported chronic pain) and 51 age- and sex-matched healthy subjects. Linear regression models determined relationships between psychophysical parameters and demographic/clinical features. Female gender, severity of disease, medical disease associated with painful symptoms, and dyskinesia were more frequently observed in PD patients experiencing pain, even though dyskinesia did not reach significance. Pain threshold and pain tolerance were significantly lower in PD patients than in control subjects, whereas the tactile threshold yielded comparable values in both groups. Multivariable linear regression analyses yielded significant inverse correlations of pain threshold and pain tolerance with motor symptom severity and Beck depression inventory. Pain threshold and pain tolerance did not differ between PD patients with and without pain. In the former group, there was no relationship between pain threshold and the intensity/type of pain, and number of painful body parts. These findings suggest that pain threshold and pain tolerance tend to decrease as PD progresses, which can predispose to pain development. Female gender, dyskinesia, medical conditions associated with painful symptoms, and postural abnormalities secondary to rigidity/bradikinesia may contribute to the appearance of spontaneous pain in predisposed subjects.


Subject(s)
Pain Threshold/physiology , Pain/etiology , Pain/psychology , Parkinson Disease/complications , Aged , Female , Humans , Male , Middle Aged , Pain Measurement , Sensory Thresholds/physiology , Severity of Illness Index
6.
J Rehabil Med ; 42(7): 691-3, 2010 Jul.
Article in English | MEDLINE | ID: mdl-20603701

ABSTRACT

OBJECTIVE: The aim of this study was to investigate the effect of botulinum toxin type A injection into the adductor muscles in reducing pain and improving joint mobility and quality of life in patients affected by hip osteoarthritis. METHODS: A total of 39 outpatients, mean age 68 years (age range 41-82 years), were evaluated using the Harris Hip Score to test hip function, a visual analogue scale to measure pain intensity and the Short Form 36 (SF-36) questionnaire to assess patient well-being and quality of life at baseline, 2, 4 and 12 weeks after treatment with botulinum toxin type A. A total of 400 U of botulinum toxin type A (Dysport) was injected into the adductor longus muscle and the adductor magnus muscle. RESULTS: The Harris Hip Score increased significantly after 2, 4 and 12 weeks (df 3, chi2 = 45.1; p < 0.0001). A significant decrease in pain intensity was detected at all the follow-up visits, after 2, 4 and 12 weeks (df 3; chi2 = 27.8; p < 0.001). The SF-36 score was significantly higher 4 and 12 weeks after treatment. At each evaluation visit a significant correlation was detected between decreased pain and improved hip mobility. CONCLUSION: Botulinum toxin type A induced a reduction in pain, indicating that this might be an innovative, less invasive treatment in patients affected by severe hip osteoarthritis, with remarkable effects on the clinical management of this disease.


Subject(s)
Botulinum Toxins, Type A/therapeutic use , Neuromuscular Agents/therapeutic use , Osteoarthritis, Hip/drug therapy , Adult , Aged , Aged, 80 and over , Botulinum Toxins, Type A/administration & dosage , Female , Humans , Injections, Intramuscular , Male , Middle Aged , Neuromuscular Agents/administration & dosage , Osteoarthritis, Hip/physiopathology , Osteoarthritis, Hip/rehabilitation , Pain Measurement , Prospective Studies , Quality of Life , Range of Motion, Articular , Surveys and Questionnaires , Treatment Outcome
7.
Neurol Sci ; 31(3): 369-72, 2010 Jun.
Article in English | MEDLINE | ID: mdl-20300793

ABSTRACT

Intravascular lymphoma is a rare subtype of diffuse large B cell lymphoma, characterized by proliferation of mature B cells within the lumina of small and medium vessels of many organs, without parenchymal involvement. The clinical phenotype is extremely variegated; moreover, neurological symptoms such as encephalopathy and focal neurological deficits occur and often coincide with disease's debut. We described the clinical course of a patient with intravascular diffuse large B cell lymphoma presented with subacute cognitive decline without focal signs, later associated to aspecific general symptoms that rapidly evolved to a severe inexplicable encephalopathy accompanied to systemic failure.


Subject(s)
Cognition Disorders/diagnosis , Lymphoma, Large B-Cell, Diffuse/diagnosis , Cognition Disorders/metabolism , Cognition Disorders/pathology , Diagnosis, Differential , Disease Progression , Fatal Outcome , Female , Humans , Lymphoma, Large B-Cell, Diffuse/metabolism , Lymphoma, Large B-Cell, Diffuse/pathology , Middle Aged , Phenotype
8.
Neuromuscul Disord ; 19(12): 849-52, 2009 Dec.
Article in English | MEDLINE | ID: mdl-19906531

ABSTRACT

The Val102fs mutation of the myelin protein zero gene (MPZ) has been associated with Charcot-Marie-Tooth disease type 1B (CMT1B). Here we describe an unusual presentation of the Val102fs mutation characterized by symptoms of spinal root hypertrophy with no overt peroneal muscular atrophy. Two sisters aged 41 and 35 years complained of neck pain and presented only pes cavus or deep-tendon hyporeflexia. In both of them magnetic resonance imaging revealed non-enhancing hypertrophy of spinal roots misdiagnosed as neurofibromatosis; neurophysiology disclosed a demyelinating neuropathy and addressed the correct molecular diagnosis. This report adds new data concerning the clinical presentations of MPZ mutations.


Subject(s)
Demyelinating Diseases/genetics , Frameshift Mutation , Myelin P0 Protein/genetics , Spinal Nerve Roots , Adult , Aged , Base Sequence , DNA Mutational Analysis , Demyelinating Diseases/pathology , Demyelinating Diseases/physiopathology , Female , Humans , Hypertrophy/genetics , Hypertrophy/pathology , Hypertrophy/physiopathology , Magnetic Resonance Imaging , Male , Molecular Sequence Data , Neck Pain/genetics , Neck Pain/pathology , Neck Pain/physiopathology , Neural Conduction , Pedigree , Siblings , Spinal Nerve Roots/pathology
9.
Neurol Sci ; 30(3): 201-5, 2009 Jun.
Article in English | MEDLINE | ID: mdl-19238315

ABSTRACT

In some definite patients, a standard neurophysiological tool may not solve a complete differential diagnosis in common nerve peroneal neuropathy. In this study we have assessed a new simple procedure to study the orthodromic sensory conduction of both the superficial peroneal nerves (SPN) and deep peroneal nerves (DPN) in a heterogeneous group of 55 normal subjects. The mean sensory orthodromic conduction velocity of the SPN was 58.35 m/s. The mean sensory orthodromic conduction velocity of the mixed nerve action potential (MNAP) of the DPN was 55.27 m/s. The sensory conduction velocity, the amplitude of sensory-evoked potentials of SPN and DPN across the fibular head and the normative values are discussed. Our results confirm that these recording methods are easy to repeat and reliable in identifying peroneal neuropathy.


Subject(s)
Electrodiagnosis/standards , Neural Conduction/physiology , Neurons, Afferent/physiology , Peripheral Nervous System Diseases/diagnosis , Peroneal Nerve/physiology , Adult , Aged , Electrodiagnosis/methods , Electrophysiology , Female , Humans , Male , Middle Aged , Reference Values , Reproducibility of Results , Young Adult
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