Intravascular large B-cell lymphoma presenting clinically as rapidly progressive dementia

Ir J Med Sci. 2018 May;187(2):319-322. doi: 10.1007/s11845-017-1653-5. Epub 2017 Jul 19.

Abstract

Background: In patients presenting with rapidly progressive dementia, prion disease may enter the differential diagnosis. The commonest malignancies masquerading as prion disease are primary CNS lymphoma and intravascular large B-cell lymphoma, both rare and difficult to diagnose without brain biopsy.

Case presentation: This 82-year-old lady with a past history of hypertension, presented with rapidly progressive cognitive impairment and ataxia. The possibility of sCJD was raised. Brain biopsy was carried out. Western blot for prion protein was negative. Brain biopsy showed intravascular large B-cell lymphoma. She died shortly afterwards.

Conclusion: The clinical presentation of intravascular large B-cell lymphoma is diverse. Patients may present as in this case with dementia, seizures, and myoclonus leading to a clinical diagnosis of sCJD. The diagnosis here was made at biopsy but is made at autopsy in over 50% of cases.

Keywords: IVLBCL—intravascular large B-cell lymphoma; PCNSL—primary CNS lymphoma; sCJD—sporadic CJD.

Publication types

  • Case Reports
  • Review

MeSH terms

  • Aged, 80 and over
  • Creutzfeldt-Jakob Syndrome / complications*
  • Creutzfeldt-Jakob Syndrome / pathology
  • Dementia / etiology*
  • Female
  • Humans
  • Ireland
  • Lymphoma, Large B-Cell, Diffuse / complications*
  • Lymphoma, Large B-Cell, Diffuse / pathology

Supplementary concepts

  • Creutzfeldt-Jakob Disease, Sporadic