Neuromyositis is a very rare type of polymyositis where, beside the us
ual muscular manifestations, there are signs of peripheral neuropathy
which can be found at clinical, electromyographic and/or pathological
examination. We have seen between 1983 and 1990 four cases of neuromyo
sitis. The neurological disorder was an axonopathy in two cases which
is usual in neuromyositis; in the other two cases, there was a polyrad
iculoneuritis which seems to be very rare in this syndrome. In the fou
r patients the disease was particularly severe and unresponsive to tre
atment. One of our patients had HTLV-I infection diagnosed by polymera
se chain reaction amplification and in situ hybridation, while the ser
ological test was negative. To our knowledge only three cases of HTLV-
I associated neuromyositis have been reported in the literature.