scholarly journals Giant cell glioblastoma in childhood-Pathohistological and immunohistochemical analysis, forecast and complex treatment

2021 ◽  
Vol 6 (7) ◽  

A six year old child is presented with giant cell glioblastoma multiforme. The importance of pathohistological and immunohistochemical analysis is discussed for the diagnosis of this rare pathohistological subtype glioblastoma in childhood. The Magnetic Resonance Image Characteristics, unfavorable prognosis and high cancer cell resistance to radiotherapy (RT) and chemotherapy (Ch) are also highlighted. The risk of local recurrences and tumor progression is high, despite the complex treatment, including visibly total tumor surgery, postoperative RT and adjuvant Ch. By this pediatric clinical case of childhood giant cell glioblastoma multiforme, we emphasize the emerging need to optimize early diagnostics and the multidisciplinary healing approach.

2019 ◽  
Vol 9 (10) ◽  
Author(s):  
Amro K. Bin Abdulrahman ◽  
Khalid A. Bin Abdulrahman ◽  
Yousef R. Bukhari ◽  
Abdulaziz M. Faqihi ◽  
Juan Gabriel Ruiz

1997 ◽  
Vol 19 (4) ◽  
pp. 385
Author(s):  
P. C. Davis ◽  
D. E. McDonnell ◽  
F. Yaghami ◽  
K. L. Satya-Prakash ◽  
A. L. Lightsey ◽  
...  

2014 ◽  
Vol 5 (3) ◽  
pp. 295 ◽  
Author(s):  
SatyaBhusan Senapati ◽  
SudhansuSekhar Mishra ◽  
SanjayKumar Behera ◽  
ManmathKumar Dhir

2019 ◽  
Vol 10 ◽  
pp. 37 ◽  
Author(s):  
Ali Akhaddar ◽  
Walter Hall ◽  
Mohammed Boucetta

Background: Cranial surgical site infections due to Salmonella species are rarely reported. Only eight cases of Salmonella enteritidis infection following intracranial surgery for brain tumor have been reported to date. We describe a unique case of both subgaleal and brain abscesses caused by S. enteritidis following craniotomy for a parafalcine giant cell glioblastoma multiforme. A literature review of the previously published cases is also provided. Case Description: A 36-year-old previously healthy man presented with a posterior parietal parafalcine giant cell glioblastoma multiforme. 5 weeks after craniotomy for tumor resection, the patient presented with worsening headache and painful swelling at the cranial operative site. Head computed tomography and magnetic resonance imaging scans revealed both scalp and brain abscesses in the previous surgical site. He was treated with aspiration of the subgaleal abscess and ciprofloxacin antibiotic therapy; he made a full recovery. Cultures of the aspirate identified S. enteritidis, although the primary site of infection was not detected. Conclusions: Although postoperative S. enteritidis infections are rare, the large numbers of patients with malignant brain tumors who require tumor resections and receive corticosteroids are at great risk. Adequate drainage (if possible), early isolation of the pathogens, and control of the infection by antibiotic therapy guided by antimicrobial susceptibility testing are vital components to prevent this potentially fatal condition.


Author(s):  
Zahra Aminparast ◽  
Mazaher Ramezani

Malignant glial tumors are rare in children. Giant cell variant is a rare subtype of glioblastoma, accounting for about 0.8% of brain tumors and 5% of glioblastoma tumors. Giant cell glioblastoma is a male predominant tumor in children and adults. Due to the low prevalence of this variant, available information is limited. An 11-year-old female child was referred with a chief complaint of a progressive persistent headache. MRI showed a well-defined cystic lesion with a solid mural component in the right parietal lobe with a compression effect on the ipsilateral ventricular system. Surgery was done. After the pathologist reported glioblastoma multiforme, a giant cell variant, the patient received 30 sessions of radiation therapy. The patient was readmitted 18 months later with a headache, and the pathologist confirmed the recurrence of the tumor. Based on radiology, the giant cell glioblastoma cannot be distinguished from the common subtype glioblastoma. The pathologists must be aware of this entity, and histologic differential diagnoses are warranted for diagnostic, prognostic, and therapeutic purposes.


Author(s):  
Amro K. Bin Abdulrahman ◽  
Yousef R. Bukhari ◽  
Abdulaziz M. Faqihi ◽  
Khalid A. Bin Abdulrahman ◽  
Juan Gabriel Ruiz

Brain cancer is the tenth leading cause of death in the U.S. Glioblastoma multiforme (GBM) is the most lethal primary malignant central nervous system tumor in adults. The present study employed samples from 1985-2014 to discover the difference in prognosis among glioblastoma subtypes after the evolution of treatment modalities over the past few years. The current study aims to find the differences between Glioblastoma multiforme (GBM) and giant cell glioblastoma (GCG) in terms of prognosis among adults and elderly patients in the U.S. This study is a historical cohort type of study and is conducted on adults and elderly individuals with GBM or GCG from the years 1985-2014 in the U.S. Data were collected from the Surveillance, Epidemiology, and End Results Program (SEER) database. The study exposure was GBM or GCG and the outcome was mortality. The potential confounders were age, sex, race, ethnicity, year of diagnosis, primary site, and surgery. A chi-square test was used for categorical data. A univariate analysis was used for variables having a p-value < 0.05. Potential confounders were selected and evaluated using multivariate logistic regression models to calculate the odds ratio with stepwise selection. The study sample was 25,117. The incidences of GBM and GCG were not similar in relation to age group. Also, Spanish-Hispanic ethnicity was independently protective of GBM and GCG as compared to Non-Spanish-Hispanic ethnicity patients with GBM have a higher mortality rate than do GCG patients. The mortality rate was higher among patients diagnosed before 2010. In conclusion, GCG was not statistically significant in association to reduced mortality. Non-Spanish-Hispanics with GBM or GCG had a higher mortality rate than did Spanish-Hispanics. Factors such as being female, being age >59, and having a year of diagnosis before 2010 were independently associated with increased mortality.


2005 ◽  
Vol 22 (3) ◽  
pp. 314-319 ◽  
Author(s):  
Prabal Deb ◽  
Mehar Chand Sharma ◽  
Bal Chander ◽  
Ashok Kumar Mahapatra ◽  
Chitra Sarkar

1995 ◽  
Vol 45 (4) ◽  
pp. 275-282 ◽  
Author(s):  
Masahito Katoh ◽  
Toshimitsu Aids ◽  
Shinji Sugimoto ◽  
Yutaka Suwamura ◽  
Hiroshi Abe ◽  
...  

2019 ◽  
Vol 7 ◽  
pp. 232470961986825
Author(s):  
Benjamin J. Delgado ◽  
Leila Moosavi ◽  
Ericka Rangel ◽  
William Stull ◽  
Rahul Dev Polineni ◽  
...  

Primary spinal cord giant cell glioblastoma multiforme of the thoracic spinal cord is a rarely-diagnosed primary spinal cord tumor in comparison to neoplasms in intracranial locations. In this article, we highlight a young adult who was diagnosed with intramedullary giant cell glioblastoma, IDH wild-type, World Health Organization grade IV/IV of the thoracic spinal cord. This case report describes the treatment approach with a postsurgical combination of radiation therapy and temozolomide, which resulted in the patient to return to her baseline of health only to later develop neurological symptoms significant for a recurrence of malignancy. In a review of the literature of described cases of primary spinal cord glioblastoma multiforme, prognosis continues to be unfavorable as current treatment options of the aggressive malignancy remain absent of a cure.


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