Cerebellar leptomeningeal enhancement: An imaging finding of rapidly progressive Purkinje cell cytoplasmic autoantibody type 1 paraneoplastic cerebellar syndrome.

J Neuroimmunol

Department of Neurology, Mayo Clinic, Rochester, MN, United States of America; Center for MS and Autoimmune Neurology, Mayo Clinic, Rochester, MN, United States of America; Department of Laboratory Medicine and Pathology, Mayo Clinic, Rochester, MN, United States of America. Electronic address:

Published: February 2024

AI Article Synopsis

  • Purkinje cell cytoplasmic autoantibody type 1 (PCA1), or anti-Yo, is linked to a severe type of cerebellar syndrome that progresses quickly and is marked by specific MRI changes, like cerebellar atrophy and T2 hyperintensity in the brainstem and spinal cord.* -
  • A new imaging finding called cerebellar leptomeningeal enhancement was noted in all three patient cases early in their illness, differing from typical cancer-related meningitis.* -
  • Despite experiencing neurological decline, all patients received immunotherapy, which led to the disappearance of leptomeningeal enhancement on follow-up MRIs, indicating a positive response to treatment.*

Article Abstract

Purkinje cell cytoplasmic autoantibody type 1 (PCA1), also known as anti-Yo, is a 'high-risk' paraneoplastic antibody, associated with rapidly progressive cerebellar syndrome. In patients with this syndrome, various MRI abnormalities have been documented, including atrophy in the cerebellum and brainstem, T2 hyperintensity in the brainstem and spinal cord, and cranial nerve enhancement. This report introduces an imaging finding, cerebellar leptomeningeal enhancement, which was observed in all three cases at early stages. Despite neurological deterioration, all patients underwent immunotherapy, and subsequent follow-up MRI revealed resolution of the leptomeningeal enhancement, suggesting that this feature is distinct from meningeal carcinomatosis.

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Source
http://dx.doi.org/10.1016/j.jneuroim.2024.578293DOI Listing

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