Abstract
Tropical spastic paraparesis (TSP) is a chronic and slowly progressive endemic myelopathy occurring in geographical isolates in the Caribbean, South India, South Africa, the Seychelles, and Colombia. A detailed clinical and laboratory study was performed on 50 TSP patients from the island of Tumaco (Colombia), in a tropical rain forest area. Most patients were middle-aged blacks, 29 (58%) men and 21 women. In every case, neurological examination confirmed the presence of pyramidal signs in the lower limbs, plus, in 58%, moderate decrease in vibratory perception distally in the feet, bilaterally and symmetrically. Absent ankle jerks were found in 28%. Slow onset and chronic progression were documented in most patients. Positive treponemal serology, from yaws infection in childhood, was found in the serum in 92%, and in 19% also in the cerebrospinal fluid (CSF). No pleocytosis was documented on 27 CSF samples, but increased protein content occurred in 86%, with elevation of gamma-globulins in 78%. Treatment of 20 patients with high doses of penicillin produced no change in the clinical picture. TSP emerges from this review of the literature as a remarkably homogeneous clinical entity worldwide. A retrovirus - human T-lymphotropic virus type 1 (HTLV-1) - has been recently implicated as a possible etiology of the syndrome.
Original language | English (US) |
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Pages (from-to) | 121-138 |
Number of pages | 18 |
Journal | Journal of the Neurological Sciences |
Volume | 87 |
Issue number | 1 |
DOIs | |
State | Published - Oct 1988 |
Externally published | Yes |
Keywords
- HTLV-1
- Myelopathy
- Neuroepidemiology
- Retroviruses
- Tropical neurology
- Tropical spastic paraparesis
ASJC Scopus subject areas
- Neurology
- Developmental Neuroscience
- Neuroscience(all)
- Surgery
- Clinical Neurology
- Aging