Objectives: Show the chronic inflammatory demyelinating polyneuropathy (CID
P) is not only clinically heterogeneous but extremely variable in severity.
Methods: Three patients were referred for mild distal paresthesiae lasting
mole than 6 months and one for inguinal and thigh pain later ascribed to co
xarthrosis. Strength was normal in all patients and tactile sensation reduc
ed distally only in one. Tendon jerks were absent, except the knee jerks in
one patient, reduced in lower limbs in two and normal in one.
Results: Electrophysiology showed a demyelinating neuropathy without motor
conduction block. CSF protein content was increased in all patients. Nerve
biopsies showed de-remyelination with varying degrees of axonal loss. Genet
ic studies excluded a demyelinating neuropathy associated with duplication
or deletion of the 17p.11.2 segment.
Conclusions: CIDP patients with pure sensory clinical presentation have bee
n described but are generally more severely impaired. However. because of t
he mildness of symptoms and the unequivocal electrophysiological involvemen
t of motor fibers, we think that in these cases the term minimal CIDP is mo
re appropriate than sensory CIDP. These cases represent the most benign end
of the CIDP spectrum. In our series minimal or even asymptomatic CIDP enco
mpasses 8% of cases. (C) 1999 Elsevier Science Ireland Ltd. All rights rese
rved.