Two patients successfully treated for prostatic cancer developed a pro
gressive neurologic syndrome beginning with loss of voluntary horizont
al eye movements followed by severe, persistent muscle spasms of the f
ace, jaw, and pharynx. Both had mild gait unsteadiness, and one exhibi
ted facial and abdominal myoclonus. Extensive diagnostic studies, incl
uding MRIs of the brainstem (with and without contrast), were normal.
CSF examination showed mild pleocytosis and elevated IgG. Quantitative
eye movement recordings documented selective involvement of voluntary
horizontal saccades with sparing of horizontal slow eye movements. Ne
ither patient had antineuronal antibodies in the blood. Postmortem exa
mination revealed perivascular chronic inflammatory cells and microgli
al infiltration of the pons and medulla. One patient also had perivasc
ular infiltrates in both mesial temporal lobes. Neuronal loss was loca
lized to the pontine tegmentum, the medullary sensory nuclei, and the
cerebellum. Brainstem motor nuclei were preserved. The clinical and pa
thologic findings suggest an autoimmune process (probably paraneoplast
ic) with selective damage to a subpopulation of brainstem neurons crit
ical for horizontal eye movements and recurrent inhibition of bulbar n
uclei.