Paraneoplastic cerebellar degeneration and Horner syndrome: association of two uncommon findings in a child with Hodgkin disease.

Abstract

An 11-year-old boy admitted with a right cervical mass was found to have Hodgkin disease. On admission, he also had right Homer syndrome and severe cerebellar ataxia. Cranial MRI revealed marked cerebellar atrophy. He was treated with chemotherapy consisting of doxorubicin, bleomycin, vinblastine, and dacarbazine (ABVD), in addition to radiotherapy. Three months after initiation of therapy, he had a partial remission of tumor. Neurologic symptoms improved dramatically after chemotherapy started. Hodgkin disease should be included in the differential diagnosis of children with cerebellar findings and Horner syndrome.

• Authors: S Emir, M T Kutluk, S Göğüş, M Büyükpamukçu
• Journal: Journal of pediatric hematology/oncology (J Pediatr Hematol Oncol) 2000 Mar-Apr Vol. 22 Issue 2 Pg. 158-61 ISSN: 1077-4114 [Print] United States
• PMID: 10779031 (Publication Type: Case Reports, Journal Article)

Topics

• Child
• Hodgkin Disease (complications, diagnosis)
• Horner Syndrome (diagnosis, etiology)
• Humans
• Magnetic Resonance Imaging
• Male
• Paraneoplastic Cerebellar Degeneration (complications, diagnosis)