Phthisis Bulbi and Leptomeningeal Metastasis in a Case of Trilateral Retinoblastoma

Rehabilitation of Phthisis Bulbi: A Case Report

Trilateral retinoblastoma: a case report.

Trilateral retinoblastoma is a rare, but well recognized syndrome. These tumors usually occur in the pineal, parasellar, or suprasellar regions several years after successful management of ocular retinoblastomas without evidence of direct extension or distant metastasis. Here we report a case of trilateral retinoblastoma presenting initially with a sellar tumor and with concurrent unilateral re...

Trilateral Retinoblastoma: a Literature

This study analyzes modern views on the history, variants, age at diagnosis of trilateral retinoblastoma, median time from retinoblastoma to trilateral retinoblastoma, the largest size and percentage of trilateral retinoblastoma among retinoblastoma cases, functions of pineal gland, genetics, ocular and intracranial histology, diagnosis, treatment, therapy results, survival rates and frequency ...

Phthisis bulbi and buphthalmos as presenting signs of retinoblastoma: a report of two cases and literature review.

PURPOSE To report two cases of bilateral retinoblastoma (RB) with unusual presentations. METHODS The medical records of 321 patients from the Retinoblastoma Referral Center in Siena were reviewed. A total of 111 patients had bilateral RB, 2 of them presenting with phthisis bulbi and buphthalmos. Both patients underwent bilateral enucleation. Clinical features, imaging studies, and histopathol...

Trilateral retinoblastoma: two variations.

Two cases of trilateral retinoblastoma (a syndrome of midline, undifferentiated, intracranial tumor in a child with hereditary, bilateral ocular retinoblastoma) are described, one with a unique location of the intracranial tumor, and the other with an unusual temporal course of disease.