Retinoblastoma

A rare eye tumor disease representing the most common intraocular malignancy in children. It is a life threatening neoplasia but is potentially curable and it can be hereditary or non hereditary, unilateral or bilateral.

Ossifying fibroma

A benign central bone tumor composed of fibrous connective tissue within which bone is formed.


Total: 3

                       


(per page)
PMID (PMCID)
1373315
 MALE Infant
Cytogenetic abnormalities in an ossifying fibroma from a patient with bilateral retinoblastoma.
Gollin SM, Storto PD, Malone PS, Barnes L, Washington JA, Chidambaram A, Janecka IP.
Genes Chromosomes Cancer. 1992;4(2):146-52.
This is the first cytogenetic analysis of a cemento-ossifying fibroma and the first report of this tumor in a retinoblastoma patient.
1373315
 MALE Infant
Cytogenetic abnormalities in an ossifying fibroma from a patient with bilateral retinoblastoma.
Gollin SM, Storto PD, Malone PS, Barnes L, Washington JA, Chidambaram A, Janecka IP.
Genes Chromosomes Cancer. 1992;4(2):146-52.
Cytogenetic analysis of a cemento-ossifying fibroma from a patient with nonfamilial bilateral multicentric retinoblastoma revealed three reciprocal translocations with the karyotype 46,XY,t(1;18)(q21;q21.3),t(3; 10)(p13;q22),t(6;11)(p22;p15).
1373315
 MALE Infant
Cytogenetic abnormalities in an ossifying fibroma from a patient with bilateral retinoblastoma.
Gollin SM, Storto PD, Malone PS, Barnes L, Washington JA, Chidambaram A, Janecka IP.
Genes Chromosomes Cancer. 1992;4(2):146-52.
Cytogenetic abnormalities in an ossifying fibroma from a patient with bilateral retinoblastoma.