Paraneoplastic cerebellar degeneration (PCD) is a rare neurological complic
ation in adults with extracerebral neoplasms. It is characterized by a diff
use cerebellar dysfunction, usually leading to severe neurological sequelae
. In childhood, this complication is extremely rare. We report on PCD as pr
imary manifestation of Hodgkin disease (HD) in a thirteen-year old boy. On
magnetic resonance imaging, irreversible atrophy of the cerebellum develope
d within three months. Antibodies against Purkinje cells were detectable at
diagnosis and normalised after successful treatment of the lymphoma. Cereb
ellar symptoms, however, only partially resolved. The necessity of a search
for a malignant tumour is emphasised in the presence of an otherwise unexp
lained, subacutely developing, diffuse cerebellar dysfunction.