Cover image of the article: Cerebellar Neuroblastoma in 2.5 Years Old Child

Image Credit:Int J Cancer Manag

Cerebellar Neuroblastoma in 2.5 Years Old Child

Authors

Mohammad Pedram1,*, Majid Vafaie1, Kiavash Fekri1, Sabahat Haghi1, Iran Rashidi2, Chia Pirooti3
1Thalassemia and Hemoglobinopathy Research Center, Ahvaz Jondishapur University of Medical Sciences, Ahvaz, Iran
2Dept. of Pathology, Shafa Hospital , Ahvaz Jondishapur University of Medical Sciences, Ahvaz, Iran
3Dept. of Neurosurgery, Golestan Hospital, Ahvaz Jondishapur University of Medical Sciences, Ahvaz, Iran
*Corresponding Author: Corresponding author: Mohammad Pedram, Thalassemia and Hemoglobinopathy Research Center, Ahvaz Jondishapur University of Medical Sciences, Ahvaz, Iran, Tel: +98-6113743285, E-mail: Email: m_pedram_2007@yahoo.com

International Journal of Cancer Management:Vol. 6, issue 3; e80434
Published online:Sep 30, 2013
Article type:Case Report
Received:Jan 02, 2012
Accepted:Feb 18, 2012
How to Cite:Pedram M, Vafaie M, Fekri K, Haghi S, Rashidi I, et al. Cerebellar Neuroblastoma in 2.5 Years Old Child. Int J Cancer Manag. 2013;6(3):e80434. doi:

Abstract

Neuroblastoma is the third most common malignancy of childhood, after leukemia and brain tumors. Only 2% of all neuroblastoma occur in the brain. Primary cerebellar neuroblastoma is an specific subset of Primitive Neuroectodermal Tumors (PNET). Meduloblastoma is a relatively common and well-established entity, consisting of primitive and multipotential cells that may exhibit some evidence of neuroblastic or gliad differentiation. But cerebellar neuroblastoma with ultrastractural evidence of significant neuroblastic differentiation is extremely rare. We report a rare case of neuroblastoma in the cerebellum. A 2.5-year-old Iranian boy presented with vomiting and nausea in the morning and ataxia. CT scan showed a tumor mass in the cerebellum and the report of radiologist was medulloblastoma. Light microscopic assay showed a small cell neoplasm with lobules of densely packed cells (lobulated pattern) and better differentiated cells. Neuron-Specific Enolase was positive. Pathologic diagnosis confirmed the existence of cerebellar neuroblastoma. Chemotherapy followed surgical removal. No relapse occurred 12 months after surgery.

Highlights

Fulltext

The Full text is available in PDF.

Copyright

© 2013, Author(s). This open-access article is available under the Creative Commons Attribution 4.0 (CC BY 4.0) International License (https://creativecommons.org/licenses/by/4.0/), which allows for unrestricted use, distribution, and reproduction in any medium, provided that the original work is properly cited.

Similar Articles

17
Nov
2018
Clinical Characteristics of Peripheral Neuroblastic Tumors in Children: A Single-Center Experience of 43 Cases

Clinical Characteristics of Peripheral Neuroblastic Tumors in Children: A Single-Center Experience of 43 Cases

Xiaokun Lin,
Guorong He,
Congde Chen,
Zhongrong Li

Lin X, He G, Chen C, Li Z. Clinical Characteristics of Peripheral Neuroblastic Tumors in Children: A Single-Center Experience of 43 Cases. Inn J Pediatr. 2018;28(6):e68834. doi: https://doi.org/10.5812/ijp.68834

15
Jan
2017
Medulloblastoma with Suprasellar Extension and Atypical Presentation

Medulloblastoma with Suprasellar Extension and Atypical Presentation

Hilwati Hashim,
Azlindarita Aisyah Mohd Abdullah,
Effat Omar,
Rofiah Ali

Hashim H, Mohd Abdullah AA, Omar E, Ali R. Medulloblastoma with Suprasellar Extension and Atypical Presentation. I J Radiol. 2017;14(2):e37942. doi: https://doi.org/10.5812/iranjradiol.37942

14
Oct
2023
Malignant Gastrointestinal Neuroectodermal Tumor: A Case Report and Literature Review

Malignant Gastrointestinal Neuroectodermal Tumor: A Case Report and Literature Review

Mahsa Ahadi,
Shirin Ziafat,
Sara Zahedifard,
Hussein Soleimantabar

Ahadi M, Ziafat S, Zahedifard S, Soleimantabar H. Malignant Gastrointestinal Neuroectodermal Tumor: A Case Report and Literature Review. Int J Cancer Manag. 2023;16(1):e135231. doi: https://doi.org/10.5812/ijcm-135231

18
Mar
2018
Low Back Pain and Paraplegia as Initial Clinical Presenting of Medulloblastoma: A Case Report

Low Back Pain and Paraplegia as Initial Clinical Presenting of Medulloblastoma: A Case Report

Kazem Anvari,
Parvaneh Dehghan,
Mohammad Reza Ehsaee,
Gholamreza Bahadorkhan

Anvari K, Dehghan P, Ehsaee MR, Bahadorkhan G. Low Back Pain and Paraplegia as Initial Clinical Presenting of Medulloblastoma: A Case Report. Int J Cancer Manag. 2018;11(3):e4315. doi: https://doi.org/10.5812/ijcm.4315

9
Nov
2024
Clinical Presentation, Treatment, and Outcomes of Pediatric Brain Tumors: A 5-Year Single-Center Experience in Istanbul

Clinical Presentation, Treatment, and Outcomes of Pediatric Brain Tumors: A 5-Year Single-Center Experience in Istanbul

Hikmet Gulsah Tanyildiz,
Yasin Yılmaz,
Şifa Şahin,
Serap Karaman,
Aysegul Unuvar,
Deniz Tugcu
,et al.

Gulsah Tanyildiz H, Yılmaz Y, Şahin Ş, Karaman S, Unuvar A, et al. Clinical Presentation, Treatment, and Outcomes of Pediatric Brain Tumors: A 5-Year Single-Center Experience in Istanbul. Inn J Pediatr. 2025;35(2):e145185. doi: https://doi.org/10.5812/ijp-145185

More by these authors

Mohammad PedramPubMedScholar
Majid VafaiePubMedScholar
Kiavash FekriPubMedScholar
Sabahat HaghiPubMedScholar
Iran RashidiPubMedScholar
Chia PirootiPubMedScholar
Share
Cited by
Metrics