Retinoblastoma classification
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Overview
Classification
Trilateral Retinoblastoma
- Trilateral retinoblastoma[1] is the term that refers to bilateral retinoblastoma associated with an intracranial primitive neuroectodermal tumor in the pineal or suprasellar region. It has a poor prognosis especially when there is leptomeningeal involvement and when the tumor spreads in to subarachnoid space. For dissemination of tumor cells into the sub-arachnoid space, Optic nerve involvement is an important portal.
- The mean length of survival is 9.7 months in patients who undergo treatment and 1.3 months in those who do not after a pineal or sellar mass is detected.[2]
References
- ↑ Provenzale JM, Weber AL, Klintworth GK, McLendon RE (1995). "Radiologic-pathologic correlation. Bilateral retinoblastoma with coexistent pinealoblastoma (trilateral retinoblastoma)". AJNR. American Journal of Neuroradiology. 16 (1): 157–65. PMID 7900586. Retrieved 2012-05-02. Unknown parameter
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