Intracranial presentation of systemic Hodgkin's disease

Khalid Hirmiz, Annette Foyle, Derek Wilke, Steven Burrell, Robert Brownstone, Casely Ago, Rajbir Pahil, Stephen Couban

Résultat de recherche: Review articleexamen par les pairs

53 Citations (Scopus)

Résumé

Intracranial involvement by Hodgkin's disease is rare. We report a patient with Hodgkin's disease who had intracranial disease at presentation. We also review the literature pertaining to intracranial Hodgkin's disease. Using the key words "Hodgkin's disease" and "central nervous system (CNS) disease", we searched the Pubmed and Cancerlit databases. References were systematically reviewed and data regarding the following variables was extracted: age, gender, signs and symptoms at presentation, histology of Hodgkin's disease, cerebrospinal fluid analysis, stage and treatment. Only 36 cases of intracranial Hodgkin's disease were identified in the literature. Intracranial Hodgkin's disease at presentation is even more uncommon with only 8 reported cases. Most cases of intracranial involvement by Hodgkin's disease occur at the time of relapse. The most common presenting feature of intracranial Hodgkin's disease is a cranial nerve palsy with brain parenchyma being the most common intracranial site of involvement. Mixed cellularity histology is the most frequent subtype of Hodgkin's disease among these patients and the median survival following intracranial presentation is 46 months. Treatment has varied extensively but includes whole brain radiation with or without combination chemotherapy. Our literature review suggests that the prognosis is not dismal with appropriate treatment.

Langue d'origineEnglish
Pages (de-à)1667-1671
Nombre de pages5
JournalLeukemia and Lymphoma
Volume45
Numéro de publication8
DOI
Statut de publicationPublished - août 2004

ASJC Scopus Subject Areas

  • Hematology
  • Oncology
  • Cancer Research

Empreinte numérique

Plonger dans les sujets de recherche 'Intracranial presentation of systemic Hodgkin's disease'. Ensemble, ils forment une empreinte numérique unique.

Citer