Neuropediatrics 2000; 31(1): 42-44
DOI: 10.1055/s-2000-15297
Short Communication

Georg Thieme Verlag Stuttgart · New York

Paraneoplastic Cerebellar Degeneration in Pediatric Hodgkin Disease

A. Hahn1 , A. Claviez2 , G. Brinkmann3 , H. J. Altermatt4 , R. Schneppenheim2 , U. Stephani1
  • 1Departments of Neuropaediatrics,
  • 2Paediatrics, and
  • 3Radiology, University of Kiel, Germany
  • 4Department of Pathology, University of Bern, Switzerland
Further Information

Publication History

August 16, 1999

November 15, 1999

Publication Date:
31 December 2000 (online)

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

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