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Updated: May 13, 2026

Endoscopic Third Ventriculostomy and Pineal Biopsy from a Single Entry Point
Published on: June 28, 2024
Decisional Tree for Pineal Tumors
Carmine Mottolese1, Federico Di Rocco2, Alexandru Szathmari2
1Pediatric Neurosurgical Service, "Woman, Child, Mother" Hospital, Rockefeller Medical School, Lyon, France. carmine.mottolese@chu-lyon.fr.
Abstract:
Pineal tumors are rare and it is important that they have to be treated by actors involved in their care. The first thing to do is the realization of the routine radiological studies necessary to establish if the tumor is located only in the pineal region or if there is bifocal localization or if the tumor is associated with a metastatic diffusion. Cerebral MRI represents the golden standard for diagnosis, associated, especially in children, to a spinal study. The study of pineal markers, the alpha protein, total human choroid gonadotrophin (hCG), and the free beta HCG, in the blood and in the CSF is of paramount importance to avoid unnecessary surgery because their presence means that we are in the face of a germ cell tumor. The age of patients is an important factor to consider because some lesions are more frequent in the pediatric age, in contrast to other tumors, which are more frequent in adult age. The decision of the choice of treatment sometimes can be difficult and for this the discussions in multidisciplinary concentration groups are necessary and these discussions should be organized also in emergencies to ensure all patients, at any time, are guaranteed of the best treatment.Surgery has a great place for treatment of benign lesion, while chemotherapy and radiotherapy have to be reserved for more malignant tumors according to the definitive histological and genetic studies of the lesions.
Insights
Accurate diagnosis of pineal tumors involves imaging like MRI and testing tumor markers. Multidisciplinary teams ensure optimal treatment, balancing surgery, chemotherapy, and radiotherapy based on tumor type and patient age.
Area of Science:
- Neuro-oncology
- Radiology
- Pediatric Oncology
Background:
- Pineal tumors are rare central nervous system neoplasms.
- Effective management requires accurate diagnosis and tailored treatment strategies.
Purpose of the Study:
- To outline diagnostic and therapeutic approaches for pineal tumors.
- To emphasize the importance of multidisciplinary care for these rare tumors.
Main Methods:
- Routine radiological studies including cerebral MRI and spinal imaging.
- Biochemical analysis of pineal markers (alpha-fetoprotein, hCG) in blood and cerebrospinal fluid (CSF).
- Consideration of patient age and tumor characteristics.
Main Results:
- Cerebral MRI is the gold standard for diagnosis.
- Elevated pineal markers indicate germ cell tumors, potentially avoiding surgery.
- Age influences tumor prevalence, with specific lesions more common in pediatric or adult populations.
Conclusions:
- Multidisciplinary team discussions are crucial for treatment decisions, even in emergencies.
- Treatment is stratified: surgery for benign lesions, chemotherapy/radiotherapy for malignant tumors based on histology and genetics.

