Multiple Sclerosis and HTLV-I associated myelopathy/tropical spastic paraparesis are two distinct clinical entities

1996 ◽  
Vol 2 (2) ◽  
pp. 88-90 ◽  
Author(s):  
Fidias E Leon-S ◽  
Kimiyoshi Arimura ◽  
Mitsuhiro Osame

Multiple sclerosis (MS) and HTLV-I associated myelopathy/tropical spastic paraparesis (HAM/TSP) can overlap in their clinical features and thereby cause difficulties for clinicians in relation to diagnosis and therapy. However, epidemiological biochemical, immunological, virological and radiological studies point to a number of significant differences. Recent comparative neurophysiological data, induding blink reflex studies, obtained in these disorders, is briefly reviewed here and provides additional evidence of difference. The abnormal blink reflex in patients with MS consist of prolonged latencies and absences of R1 and R2 responses and are mainly due to demyelinating lesions around the pons. In contrast, in HAM/TSP the blink reflex abnormalities frequently include an unusual early response, R/k, which is probably a consequence of interneuronal hyperexcitability around the brainstem. Thus these findings provide further support for our contention that HAM/TSP and multiple sclerosis are distinctly different both as clinical entities and in their underlying pathomechanisms.

2021 ◽  
Vol 24 (5) ◽  
pp. 130-137
Author(s):  
Rosa Elisa Saia ◽  
Nicola Giuseppe Frattaruolo ◽  
Cristina Malaventura ◽  
Raffaella Faggioli ◽  
Agnese Suppiej

The most common forms of paediatric vertigo are usually represented by benign causes. The occurrence of vertigo may nonetheless represent the onset of an underlying neurological disease, even without other neurological signs. The paper presents the case of a teenager with acute/subacute onset of vertigo and nausea; the examination revealed horizontal nystagmus with clinical features suggesting a peripheral form and minimal coordination defect. However, the clinical picture and persistence of symptoms led to perform brain imaging (MRI), which showed inflammatory demyelinating lesions with no signs of chronicity. These signs allowed a clinically isolated syndrome belonging to the spectrum of multiple sclerosis related disorders to be diagnosed.


2001 ◽  
Vol 119 (2) ◽  
pp. 297-305 ◽  
Author(s):  
Hirofumi Ochi ◽  
Xiao-Mu Wu ◽  
Manabu Osoegawa ◽  
Izumi Horiuchi ◽  
Motozumi Minohara ◽  
...  

2013 ◽  
Vol 113 (4) ◽  
pp. 427-433 ◽  
Author(s):  
Ali Shoeibi ◽  
Houshang Rafatpanah ◽  
Amir Azarpazhooh ◽  
Naghme Mokhber ◽  
Mohammad Reza Hedayati-Moghaddam ◽  
...  

1989 ◽  
Vol 47 (2) ◽  
pp. 134-138 ◽  
Author(s):  
C. M. de Castro Costa ◽  
M. R. Salgueiro ◽  
H. Carton ◽  
O. C. do Vale ◽  
A. M. de Arruda

Ten possible cases of tropical spastic paraparesis (TSP) in Northeastern Brazil (Ceará) are presented. They show the typical symptoms and signs of TSP consisting of weakness of the lower limbs, spastic gait, hiperreflexia, bladder dysfunction and variable signs of posterior columns impairment. The laboratory examinations excluded other compressive, infective, degenerative or demyelinating lesions of their spinal cord. Our patients age ranged from 21 to 59 years, all were of black origin and all were of lower social class. There was a slight preponderance of females. An etiological implication of a retrovirus (HTLV-I) has been shown for TSP, but for lack of technical conditions we could not determine it in our patients, and that stands as our subsequent step in those and further cases.


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