PERIPHERAL-NERVE LESIONS IN HTLV-I ASSOCIATED MYELOPATHY (HAM/TSP)

被引:34
作者
BHIGJEE, AI
BILL, PLA
WILEY, CA
WINDSOR, IM
MATTHIAS, DA
AMENOMORI, T
WACHSMAN, W
MOORHOUSE, D
机构
[1] UNIV NATAL,SCH MED,DEPT VIROL,NEUROL UNIT,DURBAN,SOUTH AFRICA
[2] UNIV NATAL,SCH MED,DEPT ANAT PATHOL,DURBAN,SOUTH AFRICA
[3] UNIV CALIF SAN DIEGO,SCH MED,DEPT PATHOL,LA JOLLA,CA 92093
[4] UNIV CALIF SAN DIEGO,SCH MED,DEPT NEUROSCI,LA JOLLA,CA 92093
[5] UNIV CALIF SAN DIEGO,SCH MED,DIV HAEMATOL ONCOL,LA JOLLA,CA 92093
[6] SAN DIEGO VAMC,RES SERV,SAN DIEGO,CA
关键词
HAM/TSP; NEUROPATHY; DEMYELINATION; GLOBULES; NO ANTIGEN;
D O I
10.1002/mus.880160106
中图分类号
R74 [神经病学与精神病学];
学科分类号
摘要
Peripheral nerve dysfunction (PND) was found in as many as 43% of our patients with human T-cell lymphotropic virus type I (HTLV-I)-associated myelopathy (HAM/TSP). To evaluate the PND further we biopsied the sural nerve in 6 patients. The histological features were varying degrees of demyelination, demyelination, axonal atrophy and degeneration, and perineurial fibrosis. ''Globule'' or ''sausage'' formation was prominent in two of the specimens. Inflammatory infiltrates were absent. No deposits of IgG, IgM, IgA, or complement were detected in the biopsies. No viral antigen or proviral DNA was detected. It is proposed that the PND and the histological findings noted are part of HTLV-I-associated disease and not an unrelated disorder. The pathogenesis of the PND remains unclear. There was no evidence of direct viral infection. The histological findings could represent primary changes induced by viral-triggered release of soluble factors, such as cytokines or secondary changes to more proximal disease, e.g., root involvement.
引用
收藏
页码:21 / 26
页数:6
相关论文
共 23 条
[1]   AN AUTOPSY CASE OF HUMAN T-LYMPHOTROPIC VIRUS TYPE-I-ASSOCIATED MYELOPATHY [J].
AKIZUKI, S ;
SETOGUCHI, M ;
NAKAZATO, O ;
YOSHIDA, S ;
HIGUCHI, Y ;
YAMAMOTO, S ;
OKAJIMA, T .
HUMAN PATHOLOGY, 1988, 19 (08) :988-990
[2]   CLINICAL ELECTROPHYSIOLOGIC STUDIES OF HTLV-I-ASSOCIATED MYELOPATHY [J].
ARIMURA, K ;
ROSALES, R ;
OSAME, M ;
IGATA, A .
ARCHIVES OF NEUROLOGY, 1987, 44 (06) :609-612
[3]   JAMAICAN NEUROPATHY - AN ELECTROPHYSIOLOGICAL STUDY [J].
BARKHAUS, PE ;
MORGAN, O .
MUSCLE & NERVE, 1988, 11 (04) :380-385
[4]  
BEHSE F, 1990, Acta Neurologica Scandinavica Supplementum, V82, P1
[5]   DETECTION OF HUMAN T-CELL LYMPHOMA LEUKEMIA-VIRUS TYPE-I DNA AND ANTIGEN IN SPINAL-FLUID AND BLOOD OF PATIENTS WITH CHRONIC PROGRESSIVE MYELOPATHY [J].
BHAGAVATI, S ;
EHRLICH, G ;
KULA, RW ;
KWOK, S ;
SNINSKY, J ;
UDANI, V ;
POIESZ, BJ .
NEW ENGLAND JOURNAL OF MEDICINE, 1988, 318 (18) :1141-1147
[6]   MYELOPATHY ASSOCIATED WITH HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE-I (HTLV-I) IN NATAL, SOUTH-AFRICA - A CLINICAL AND INVESTIGATIVE STUDY IN 24 PATIENTS [J].
BHIGJEE, AI ;
KELBE, C ;
HARIBHAI, HC ;
WINDSOR, IM ;
HOFFMANN, MH ;
MODI, G ;
BILL, PLA ;
BECKER, WB ;
SINGH, B ;
ENGELBRECHT, S .
BRAIN, 1990, 113 :1307-1320
[7]   RECURRENT BRACHIAL-PLEXUS NEUROPATHY [J].
BRADLEY, WG ;
MADRID, R ;
THRUSH, DC ;
CAMPBELL, MJ .
BRAIN, 1975, 98 (SEP) :381-+
[8]  
COSNETT J. E., 1965, S AFRICAN MED J, V39, P592
[9]   TROPICAL SPASTIC PARAPARESIS AND HUMAN T-CELL LYMPHOTROPIC VIRUS TYPE-1 IN THE UNITED-KINGDOM [J].
CRUICKSHANK, JK ;
RUDGE, P ;
DALGLEISH, AG ;
NEWTON, M ;
MCLEAN, BN ;
BARNARD, RO ;
KENDALL, BE ;
MILLER, DH .
BRAIN, 1989, 112 :1057-1090
[10]   CELLULAR PATHOLOGY OF THE NERVE MICROENVIRONMENT IN GALACTOSE INTOXICATION [J].
FORCIER, NJ ;
MIZISIN, AP ;
RIMMER, MA ;
POWELL, HC .
JOURNAL OF NEUROPATHOLOGY AND EXPERIMENTAL NEUROLOGY, 1991, 50 (03) :235-255