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Leptomeningeal dissemination of a low-grade lumbar paraganglioma: case report.
Thomson, Nick; Pacak, Karel; Schmidt, Meic; Palmer, Cheryl; Salzman, Karen; Champine, Marjan; Schiffman, Joshua; Cohen, Adam.
Affiliation
  • Thomson N; Department of Internal Medicine, University of Arizona College of Medicine Phoenix, Arizona
  • Pacak K; Section on Medical Neuroendocrinology, Eunice Kennedy Shriver National Institute of Child Health and Human Development, National Institutes of Health, Bethesda, Maryland
  • Schmidt MH; Department of Neurosurgery, University of Utah, Salt Lake City, Utah
  • Palmer CA; Huntsman Cancer Institute, Salt Lake City, Utah
  • Salzman KL; Department of Pathology, Division of Anatomic Pathology, University of Utah, Salt Lake City, Utah
  • Champine M; Huntsman Cancer Institute, Salt Lake City, Utah
  • Schiffman JD; Department of Radiology, Division of Neuroradiology, University of Utah, Salt Lake City, Utah
  • Cohen AL; Huntsman Cancer Institute, Salt Lake City, Utah
J Neurosurg Spine ; 26(4): 501-506, 2017 04.
Article in En | MEDLINE | ID: mdl-28128698
Leptomeningeal dissemination of paraganglioma is rare, with only 2 prior cases in the literature. The authors present the case of a metastatic low-grade lumbar paraganglioma via leptomeningeal dissemination. This report emphasizes the utility of 3,4-dihydroxy-6-18F-fluoro-l-phenylalanine (18F-FDOPA) PET scanning for diagnosis, as well as the combination of radiation therapy and alkylating chemotherapeutic agents for the treatment of this rare phenomenon. The patient was a 61-year-old woman who presented with low-back pain and was found to have an isolated L-3 intrathecal tumor on MRI. Sixteen months after gross-total en bloc resection of the paraganglioma, the patient again became symptomatic with new neurological symptoms. MRI findings revealed enhancing leptomeningeal nodules throughout the spine. 18F-FDOPA PET/CT scanning was used to confirm the diagnosis of disseminated paraganglioma. Intrathecal thiotepa, radiation therapy, and systemic therapy with capecitabine and temozolomide have been used sequentially over a 2-year period, with each able to stabilize tumor growth for several months. The authors also summarize the 2 other reports of leptomeningeal dissemination of paragangliomas in the literature and compare the course and management of the 3 cases.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Paraganglioma / Spinal Cord Neoplasms / Meningeal Neoplasms Type of study: Diagnostic_studies / Etiology_studies Limits: Female / Humans / Middle aged Language: En Journal: J Neurosurg Spine Journal subject: NEUROCIRURGIA Year: 2017 Type: Article

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Paraganglioma / Spinal Cord Neoplasms / Meningeal Neoplasms Type of study: Diagnostic_studies / Etiology_studies Limits: Female / Humans / Middle aged Language: En Journal: J Neurosurg Spine Journal subject: NEUROCIRURGIA Year: 2017 Type: Article