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Adult hippocampal ganglioneuroblastoma: Case report and literature review.

Abstract Intracranial ganglioneuroblastoma represents a rare subtype of primitive neuroectodermal tumor. Here, we report a hippocampal ganglioneuroblastoma and a literature review of cerebral anglioneuroblastoma is carried out.
PMID
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Authors

Mayor MeshTerms
Keywords
Journal Title medicine
Publication Year Start




PMID- 29390424
OWN - NLM
STAT- MEDLINE
DCOM- 20180213
LR  - 20180213
IS  - 1536-5964 (Electronic)
IS  - 0025-7974 (Linking)
VI  - 96
IP  - 51
DP  - 2017 Dec
TI  - Adult hippocampal ganglioneuroblastoma: Case report and literature review.
PG  - e8894
LID - 10.1097/MD.0000000000008894 [doi]
AB  - RATIONALE: Intracranial ganglioneuroblastoma represents a rare subtype of
      primitive neuroectodermal tumor. Here, we report a hippocampal
      ganglioneuroblastoma and a literature review of cerebral anglioneuroblastoma is
      carried out. PATIENT CONCERNS: We report a 16-year-old male patient presenting
      with absence seizure and high-infiltration hippocampal ganglioneuroblastoma.
      INTERVENTIONS: Magnetic resonance imaging (MRI) indicates a space-occupying
      lesion with a well-defined margin in the right temporal lobe and hippocampus.
      However, hyper-signal on flair and diffusion-weighted imaging (DWI) with a low
      apparent diffusion coefficient (ADC) value is detected, which prompts high
      tumoral invasiveness. INTERVENTIONS: A total resection of tumor and subsequent
      chemotherapy combing with radiotherapy is performed. OUTCOMES: For a follow-up
      period of 60 months, no evidence of recurrence and further seizures are detected.
      LESSONS: High-infiltration hippocampal ganglioneuroblastoma is a rare event. MRI 
      examination often showed features of low-grade gliomas, while hyper-signal lesion
      on DWI with a low ADC value can be detected. Complete resection combined with
      fractionated radiotherapy and chemotherapy was the optimal treatment for cerebral
      ganglioneuroblastoma.
CI  - Copyright (c) 2017 The Authors. Published by Wolters Kluwer Health, Inc. All
      rights reserved.
FAU - Yao, Pei-Sen
AU  - Yao PS
AD  - Department of Neurosurgery.
FAU - Chen, Guo-Rong
AU  - Chen GR
AD  - Department of Neurosurgery.
FAU - Shang-Guan, Huang-Cheng
AU  - Shang-Guan HC
AD  - Department of Critical Medicine.
FAU - Lin, Qing-Song
AU  - Lin QS
AD  - Department of Neurosurgery.
FAU - Wang, Xing-Fu
AU  - Wang XF
AD  - Department of Pathology, the First Affiliated Hospital of Fujian Medical
      University, Fuzhou, China.
FAU - Zheng, Shu-Fa
AU  - Zheng SF
AD  - Department of Neurosurgery.
FAU - Kang, De-Zhi
AU  - Kang DZ
AD  - Department of Neurosurgery.
LA  - eng
PT  - Case Reports
PT  - Journal Article
PL  - United States
TA  - Medicine (Baltimore)
JT  - Medicine
JID - 2985248R
SB  - AIM
SB  - IM
MH  - Adolescent
MH  - Brain Neoplasms/complications/*diagnosis/diagnostic imaging/therapy
MH  - Combined Modality Therapy
MH  - Diagnosis, Differential
MH  - Ganglioneuroblastoma/complications/*diagnosis/diagnostic imaging/therapy
MH  - Hippocampus
MH  - Humans
MH  - Magnetic Resonance Imaging
MH  - Male
MH  - Seizures/etiology
PMC - PMC5758126
EDAT- 2018/02/03 06:00
MHDA- 2018/02/14 06:00
CRDT- 2018/02/03 06:00
PHST- 2018/02/03 06:00 [entrez]
PHST- 2018/02/03 06:00 [pubmed]
PHST- 2018/02/14 06:00 [medline]
AID - 10.1097/MD.0000000000008894 [doi]
AID - 00005792-201712220-00011 [pii]
PST - ppublish
SO  - Medicine (Baltimore). 2017 Dec;96(51):e8894. doi: 10.1097/MD.0000000000008894.