Spinal en plaque meningiomas: a contemporary experience

Emanuela Caroli1, Michele Acqui, Raffaelino Roperto

  • 1Department of Neurological Sciences and Neurosurgery, Policlinico S. Andrea, University of Rome La Sapienza, Rome, Italy. manucarol2000@yahoo.it

Neurosurgery
|December 3, 2004
PubMed
Abstract

Insights

Spinal en plaque meningiomas are rare tumors that often cause arachnoiditis, making surgical treatment difficult. These tumors have a poorer prognosis than classic meningiomas due to frequent recurrence and postoperative complications.

Area of Science:

  • Neurosurgery
  • Spinal Oncology
  • Neuropathology

Background:

  • Spinal en plaque meningiomas are rare dural tumors characterized by their diffuse, flattened growth pattern along the spinal cord.
  • These lesions present unique surgical challenges due to their infiltrative nature and frequent association with spinal arachnoiditis, complicating dissection and increasing the risk of neurological injury.

Observation:

  • This study reviewed seven cases of spinal en plaque meningiomas and conducted a literature search to analyze all reported cases.
  • Microsurgery was the primary treatment modality, with complete tumor resection achieved in three patients and subtotal resection in four.
  • One patient experienced permanent neurological worsening postoperatively.

Findings:

  • Spinal en plaque meningiomas exhibit a poorer prognosis compared to classic meningiomas regarding definitive surgical cure.
  • High rates of recurrence and postoperative arachnoiditis contribute to the less favorable outcomes.
  • Complete tumor removal is feasible only when a distinct cleavage plane between the tumor and the arachnoid mater is present.

Implications:

  • Surgical strategies for spinal en plaque meningiomas must carefully consider the risk of arachnoiditis and recurrence.
  • Careful patient selection and surgical technique are crucial to optimize outcomes and minimize neurological deficits.
  • Further research into adjuvant therapies or novel surgical approaches may be warranted to improve the prognosis of these challenging tumors.

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