Outcome and Prognosis
The prognosis for patients with pineal region tumors is dependent upon tumor histology and is subject to change as more effective adjuvant therapy is developed. In general, patients with intracranial germinomas have an excellent prognosis because of the radiosensitivity of these tumors.
Children with nongerminomatous germ cell tumors have a significantly worse prognosis than do children with germinomas or pineal cell tumors. No conventional approach is designed for managing recurrence. Chemotherapy, radiotherapy, or radiosurgery can be applied if maximal doses have not already been administered. A second surgical procedure is generally reserved for patients with benign lesions who demonstrate recurrence several years later.
Recurrent germ cell tumors have been shown to respond to chemotherapy, as have some pineal cell tumors, although to a lesser degree. Radiosurgery may be a consideration for all recurrences less than 3 cm in diameter.
Future and Controversies
Pineal region tumors represent a rare but challenging problem for the neurologist, neurosurgeon, and clinical oncologist. Therapeutic and diagnostic advances in several disciplines have significantly improved the prognosis of patients with these lesions. The authors remain hopeful that current clinical and basic science research will help refine therapies and further augment survival rates while lowering morbidity.
The authors and editors of eMedicine gratefully acknowledge the contributions of previous authors Andrew T Parsa, MD, PhD, and Chris E Mandigo, MD.
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Further Reading
Keywords
pineal, tumors, pineal tumor, pineal tumors, pineal gland, pineal gland tumors, pineal gland tumor, pineal region tumors, pineoblastomas, pineocytomas, pineal germ cell tumors, germinomas, pineal gliomas, pineal metastasis, obstructive hydrocephalus, vertical gaze palsy, astrocytomas, meningiomas, teratomas, pineal cyst, pineal cysts
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