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Embryonal central nervous system neoplasms arising in infants and young children: a pediatric brain tumor consortium study.

Publication ,  Journal Article
McLendon, RE; Adekunle, A; Rajaram, V; Koçak, M; Blaney, SM
Published in: Arch Pathol Lab Med
August 2011

CONTEXT: Medulloblastomas (MBs) and atypical teratoid/rhabdoid tumors (AT/RTs) arising in infants and children can be difficult to distinguish; however, histologic characterization is prognostically important. OBJECTIVE: To determine histologic and phenotypic markers associated with utility with progression-free survival (PFS) and overall survival (OS) in children younger than 3 years with MBs and AT/RTs. DESIGN: We undertook a histologic and immunophenotypic study of MBs and AT/RTs arising in infants and children younger than 3 years treated in a Pediatric Brain Tumor Consortium study. The 41 girls and 55 boys ranged in age from 2 to 36 months at enrollment. These infants and children exhibited 51 MBs, 26 AT/RTs, and 24 other tumors (not further studied). Median follow-up of the patients was 17.2 months from diagnosis (range: 1.4-93 months). RESULTS: Infants and children with AT/RT exhibited a statistically significant shorter PFS and OS when compared to infants and children with MBs (both P < .001). A lack of nuclear BAF47 immunohistochemical reactivity proved reliable in identifying AT/RTs. Among MBs, our data suggest an association of nodularity and prolonged PFS and OS, which must be independently confirmed. Anaplasia correlated with OTX2 reactivity and both OTX2 and moderate to severe anaplasia correlated with PFS but not with OS. CONCLUSION: Distinguishing AT/RT from MBs is clinically important. For expert neuropathologists, the diagnoses of AT/RT and MB can be reliably made from hematoxylin-eosin stains in the vast majority of cases. However certain rare small cell variants of AT/RT can be confused with MB. We also found that immunohistochemical reactivity for BAF47 is clinically useful in distinguishing MBs from AT/RTs and for identifying certain small cell AT/RTs. Among MBs, nodularity may be an important prognostic factor for improved PFS and OS in infants and children.

Duke Scholars

Published In

Arch Pathol Lab Med

DOI

EISSN

1543-2165

Publication Date

August 2011

Volume

135

Issue

8

Start / End Page

984 / 993

Location

United States

Related Subject Headings

  • Transcription Factors
  • Teratoma
  • Survival Rate
  • SMARCB1 Protein
  • Rhabdoid Tumor
  • Prognosis
  • Pathology
  • Medulloblastoma
  • Male
  • Infant
 

Citation

APA
Chicago
ICMJE
MLA
NLM
McLendon, R. E., Adekunle, A., Rajaram, V., Koçak, M., & Blaney, S. M. (2011). Embryonal central nervous system neoplasms arising in infants and young children: a pediatric brain tumor consortium study. Arch Pathol Lab Med, 135(8), 984–993. https://doi.org/10.5858/2010-0515-OAR1
McLendon, Roger E., Adesina Adekunle, Veena Rajaram, Mehmet Koçak, and Susan M. Blaney. “Embryonal central nervous system neoplasms arising in infants and young children: a pediatric brain tumor consortium study.Arch Pathol Lab Med 135, no. 8 (August 2011): 984–93. https://doi.org/10.5858/2010-0515-OAR1.
McLendon RE, Adekunle A, Rajaram V, Koçak M, Blaney SM. Embryonal central nervous system neoplasms arising in infants and young children: a pediatric brain tumor consortium study. Arch Pathol Lab Med. 2011 Aug;135(8):984–93.
McLendon, Roger E., et al. “Embryonal central nervous system neoplasms arising in infants and young children: a pediatric brain tumor consortium study.Arch Pathol Lab Med, vol. 135, no. 8, Aug. 2011, pp. 984–93. Pubmed, doi:10.5858/2010-0515-OAR1.
McLendon RE, Adekunle A, Rajaram V, Koçak M, Blaney SM. Embryonal central nervous system neoplasms arising in infants and young children: a pediatric brain tumor consortium study. Arch Pathol Lab Med. 2011 Aug;135(8):984–993.

Published In

Arch Pathol Lab Med

DOI

EISSN

1543-2165

Publication Date

August 2011

Volume

135

Issue

8

Start / End Page

984 / 993

Location

United States

Related Subject Headings

  • Transcription Factors
  • Teratoma
  • Survival Rate
  • SMARCB1 Protein
  • Rhabdoid Tumor
  • Prognosis
  • Pathology
  • Medulloblastoma
  • Male
  • Infant