Here we report a patient with a lymphoepithelial thymoma who developed in c
hronological sequence limbic encephalitis, neuromyotonia and myasthenia gra
vis.
The patient presented with limbic encephalitis associated with an invasive
thymoma and improved after surgery and cytotoxic therapy. Two months after
thymectomy, neuromyotonia associated with hyperhidrosis and mild motor neur
opathy occurred and the patient was given plasma-exchange and prednisone th
erapy. Five months later he developed mild generalised myasthenia gravis. A
nti-acetylcholine receptor antibodies, previously repeatedly negative, were
found positive at the onset of clinical signs of myasthenia gravis. (C) 19
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