Primary diffuse leptomeningeal gliomatosis followed with serial magnetic resonance images

Satoshi Ishige1, Yasuo Iwadate, Hiroshi Ishikura

  • 1Department of Neurological Surgery, Chiba University Graduate School of Medicine 1-8-1, Inohana, Chuo-ku, 260-8670 Chiba, Japan.

Insights

Primary diffuse leptomeningeal gliomatosis (PDLG) is a rare condition. Serial magnetic resonance imaging (MRI) aids in diagnosing PDLG by revealing characteristic leptomeningeal enhancement.

Area of Science:

  • Neuro-oncology
  • Neuroradiology
  • Neuropathology

Background:

  • Primary diffuse leptomeningeal gliomatosis (PDLG) is a rare neoplastic condition characterized by diffuse infiltration of the leptomeninges by glial tumor cells.
  • Distinguishing PDLG from other leptomeningeal diseases can be challenging due to overlapping imaging features.

Observation:

  • A 45-year-old male presented with bilateral abducens nerve palsy and meningeal signs.
  • Serial magnetic resonance imaging (MRI) demonstrated diffuse leptomeningeal enhancement across the central nervous system.
  • Imaging findings included ventricular dilatation and enlarged cerebral sulci, without an identifiable intra-axial mass.

Findings:

  • Brain biopsy confirmed the diagnosis of leptomeningeal gliomatosis.
  • The observed MRI patterns are indicative of PDLG.

Implications:

  • Serial MRI is crucial for the diagnosis of PDLG.
  • Recognizing these specific MRI findings can aid in differentiating PDLG from other conditions with diffuse leptomeningeal spread.
  • This case highlights the importance of integrating clinical, radiological, and pathological findings for accurate PDLG diagnosis.