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Clinicopathological spectrum of central nervous system germ cell tumors: A single-institution retrospective study
Sreelekha Appasani1, Neelima Radhakrishnan2, Anitha Mathews2
1Department of Pathology, Sri Venkateswara Institute of Medical Sciences, Tirupati, Andhra Pradesh, India.
Context:
Central nervous system germ cell tumors (CNSGCTs) though rare is the second most common extragonadal site for GCTs.
Aims:
To determine the clinicopathological features of CNSGCTs diagnosed at our center.
Settings And Design:
A retrospective study of all histologically diagnosed CNSGCTs, during 2006-2019.
Materials And Methods:
The patients' data were retrieved from the hospital information systems and analyzed.
Statistical Analysis:
Data on categorical variables were analyzed as percentages, and data on continuous variables calculated as mean. Chi-square test or Fisher's exact test was used to study association between variables.
Results:
Of the total 34 cases with CNSGCT, age ranged from 1 to 27 years, majority in the second decade (19/34; 56%). Male: female (M: F) ratio was 1.6:1. Single site involvement was seen in 27 cases (27/34; 79%), whereas seven (7/34; 21%) showed bi/multifocal involvement. Among the unifocal cases, common sites involved were suprasellar (12/27; 44.4%), closely followed by the pineal (10/27; 37%). All multifocal tumors affected suprasellar compartment, being bifocal with pineal in four cases. A male gender predilection was noted among pineal region (9/10;90%) and multifocal tumors (5/7;71%). Germinoma was the commonest subtype (21/34; 61.8%) with male gender predilection (17/21; 81%) (M: F =4.3:1), with female predilection seen among mixed GCTs (MGCTs) (8/10; 80%) (M: F =1:4) and suprasellar location (M: F =1:2). Serum tumor markers (25 cases) and CSF markers (7 cases) were concordant with histology in all, except two cases.
Conclusion:
Though histology and immunohistochemistry were diagnostic, correlation between serum and/or CSF marker was essential to rule out GCT component(s) that may be missed on biopsy due to sampling error.
Insights
Central nervous system germ cell tumors (CNSGCTs) are rare but important extragonadal sites. This study details their clinicopathological features, highlighting germinoma as the most common subtype and the importance of tumor markers.
Area of Science:
- Neuro-oncology
- Pathology
- Oncology
Background:
- Central nervous system germ cell tumors (CNSGCTs) are rare neoplasms.
- The central nervous system (CNS) is the second most common extragonadal site for germ cell tumors (GCTs).
Purpose of the Study:
- To determine the clinicopathological features of CNSGCTs.
- To analyze the distribution, subtypes, and demographic predilections of CNSGCTs.
Main Methods:
- Retrospective analysis of histologically diagnosed CNSGCT cases from 2006-2019.
- Data collected from hospital information systems.
- Statistical analysis using percentages, means, Chi-square, and Fisher's exact tests.
Main Results:
- 34 CNSGCT cases analyzed; age range 1-27 years, majority in second decade.
- Germinoma was the most common subtype (61.8%), with male predilection.
- Suprasellar and pineal regions were common sites; multifocal involvement noted in 21%.
Conclusions:
- Histology and immunohistochemistry are crucial for CNSGCT diagnosis.
- Correlation of serum and/or CSF tumor markers with histology is essential.
- Tumor markers help identify GCT components missed by biopsy sampling.
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