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The role of methylation profiling in histologically diagnosed neurocytoma: a case series.
Kalawi, Adam Z; Malicki, Denise M; Abdullaev, Zied; Pratt, Drew W; Quezado, Martha; Aldape, Kenneth; Elster, Jennifer D; Paul, Megan R; Khanna, Paritosh C; Levy, Michael L; Crawford, John R.
Affiliation
  • Kalawi AZ; Division of Child Neurology, Department of Neurosciences, University of California, San Diego, CA, USA. Azkalawi@health.ucsd.edu.
  • Malicki DM; Rady Children's Hospital, San Diego, CA, USA. Azkalawi@health.ucsd.edu.
  • Abdullaev Z; Rady Children's Hospital, San Diego, CA, USA.
  • Pratt DW; Department of Pathology, University of California, San Diego, CA, USA.
  • Quezado M; Laboratory of Pathology, National Cancer Institute, Bethesda, MD, USA.
  • Aldape K; Department of Pathology, University of Michigan, Ann Arbor, MI, USA.
  • Elster JD; Laboratory of Pathology, National Cancer Institute, Bethesda, MD, USA.
  • Paul MR; Laboratory of Pathology, National Cancer Institute, Bethesda, MD, USA.
  • Khanna PC; Rady Children's Hospital, San Diego, CA, USA.
  • Levy ML; Division of Hematology Oncology, Department of Pediatrics, University of California, San Diego, CA, USA.
  • Crawford JR; Rady Children's Hospital, San Diego, CA, USA.
J Neurooncol ; 159(3): 725-733, 2022 Sep.
Article in En | MEDLINE | ID: mdl-35994156
ABSTRACT

PURPOSE:

To highlight the clinical, neuroradiographic, neuropathologic, and molecular features of histologically identified neurocytoma in a pediatric cohort and highlight the evolving use methylation profiling in providing diagnostic clarity in difficult to diagnosis pediatric brain tumors.

METHODS:

Five consecutive children (ages 9-13, 2 girls 3 boys) were histologically diagnosed with neurocytoma at Rady Children's Hospital San Diego from 2012 to 2018. Clinical and molecular features were analyzed with regards to treatment course and outcome.

RESULTS:

Presenting symptoms included seizures (n = 2), syncope (n = 1), headache (n = 2), visual disturbances (n = 2) and emesis (n = 2). Tumor location included intraventricular (n = 2), intraventricular with parenchymal spread (n = 1), and extraventricular (n = 2). Magnetic resonance imaging demonstrated reduced diffusivity (2/5), signal abnormality on susceptibility-weighted sequences (3/5), and varying degrees of contrast enhancement (4/5). All patients underwent surgical resection alone. Recurrence occurred in four children that were treated with surgery (4/4), adjuvant radiation (2/4), and chemoradiation (1/4). Neuropathologic features included positivity for GFAP (4/5), synaptophysin (4/5), NSE (2/2), NeuN (4/4), and variable Ki-67 (< 1% to 15%). Next generation sequencing (3/5) and microarray (3/5) collectively were abnormal in four of five tumors. Methylation profiling was successfully performed on four of five samples which led to modification of diagnosis in two patients and the others were either unclassifiable or confirmatory with the histologic diagnosis. Mean time to follow up was 77 months (range 44-112 months). Mean progression free survival and overall survival were 24 months (range 6 to 52 months) and 100% respectively.

CONCLUSION:

Neurocytomas are a rare clinical entity that warrants further investigation into molecular and pathologic prognosticating features. Methylation profiling may aid in differentiation of neurocytoma from other difficult to diagnose tumors who share similar histologic features.
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Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Neurocytoma Type of study: Diagnostic_studies / Prognostic_studies Limits: Child / Female / Humans / Male Language: En Journal: J Neurooncol Year: 2022 Type: Article Affiliation country: United States

Full text: 1 Collection: 01-internacional Database: MEDLINE Main subject: Brain Neoplasms / Neurocytoma Type of study: Diagnostic_studies / Prognostic_studies Limits: Child / Female / Humans / Male Language: En Journal: J Neurooncol Year: 2022 Type: Article Affiliation country: United States