HTLV-I ASSOCIATED MYELOPATHY, A NEW CLINICAL ENTITY
HTLV-I ASSOCIATED MYELOPATHY, A NEW CLINICAL ENTITY
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DOI:
10.1016/s0140-6736(86)91298-5
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发表时间:
1986-05
期刊:
影响因子:
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通讯作者:
M. Osame;K. Usuku;S. Izumo;N. Ijichi;H. Amitani;A. Igata;M. Matsumoto;M. Tara
中科院分区:
文献类型:
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作者:
M. Osame;K. Usuku;S. Izumo;N. Ijichi;H. Amitani;A. Igata;M. Matsumoto;M. Tara
The correspondents comment on the reports of Gessainet al.(above). They also report 6 patients (4 women, 2 men) aged 25-58 years, with slowly progressive spastic paraparesis. These cases were seen in the Kagoshima prefecture of Japan, where the prevalence of anti-HTLV-I is about 16%. The 6 had very high anti-HTLV-I titres by latex agglutination in serum (512-8192) and in CSF (64-512). Out of 78 neurological control patients 12 were seropositive (serum titre 16-2048). Only one control had anti-HTLV-I in CSF. In the paraparetic patients Western blot of CSF showed 2 clear bands (p24 and p32). Their white blood cell counts were normal though ATLL-associated lymphocyte appearances were seen in some. Four of 6 were treated with prednisolone in a tapering dose with improvement in gait, sensation and sphincter control. Subsequently Western blot anti-HTLV-I testing of the CSF of previously undiagnosed patients has revealed 7 more cases. The authors suggest that this spastic paraparesis be called HTLV-I-associated myelopathy (HAM).In a subsequent letter (ibid., ii,104-105) they report a further 17 cases, who also lived in Kagoshima prefecture. Nine (39%) of the 23 cases had had a blood transfusion before onset of symptoms, a much higher frequency than in 3 control groups; patients with adult T-cell leukaemia/lymphoma, internal medicine inpatients, and hospital staff.newline˜P. Mortimer