HUMAN T-LYMPHOTROPIC VIRUS TYPE-I DNA IN SPINAL-CORD OF TROPICAL SPASTIC PARAPARESIS WITH CONCOMITANT HUMAN T-LYMPHOTROPIC VIRUS TYPE-I NEGATIVE HODGKINS-DISEASE
L. Navarroroman et al., HUMAN T-LYMPHOTROPIC VIRUS TYPE-I DNA IN SPINAL-CORD OF TROPICAL SPASTIC PARAPARESIS WITH CONCOMITANT HUMAN T-LYMPHOTROPIC VIRUS TYPE-I NEGATIVE HODGKINS-DISEASE, Human pathology, 25(10), 1994, pp. 1101-1106
We studied a 58-year-old black woman from Barbados who simultaneously
developed myelopathy and lymphoma with human T-lymphotropic virus type
I (HTLV-I) antibodies in serum and cerebrospinal fluid and died 3 yea
rs after onset. Neuropathological examination showed typical tropical
spastic paraparesis (TSP). The polymerase chain reaction (PCR) demolzs
trated defective proviral genome retaining the HTLV-I pX and env regio
ns in thoracic spinal cord, the level most severely affected. Defectiv
e HTLV-I in the nervous system retaining the pX region may be relevant
to pathogenesis because circulating CD8+ cytotoxic lymphocytes specif
ic for HTLV-I pX occur in HTLV-I myelopathy. This patient's lymph node
biopsy specimen was consistent with Hodgkin's disease (HD), nodular s
clerosis subtype, of B-cell origin. The PCR in the paraffin-embedded l
ymph node involved by HC, failed to amplify HTLV-I poviral sequences.
Complete HTLV-I proviral amplification was obtained in paraffin-embedd
ed lymph nodes from positive controls (adult T-cell leukemia). To our
knowledge the association of TSP and HD has not been reported previous
ly. Despite claims that HD may be associated with HTLV-I, we demonstra
ted absence of HTLV-I-infected T cells in the lymphoid infiltrate of H
D in this case, positive HTLV-I serology notwithstanding.