Literature DB >> 6339032

Ewing's tumor following bilateral retinoblastoma. A case report.

S Schifter, L Vendelbo, O M Jensen, S Kaae.   

Abstract

Retinoblastoma is found in a hereditary and nonhereditary form. Long survivors treated for the hereditary form seem to be predisposed for developing a second primary tumor later in life. The retinoblastoma genes are supposed to be responsible for this disposition. This report describes the development of a Ewing's tumor in a nine-year-old girl, who had both eyes removed in early life for retinoblastoma.

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Year:  1983        PMID: 6339032     DOI: 10.1002/1097-0142(19830501)51:9<1746::aid-cncr2820510930>3.0.co;2-g

Source DB:  PubMed          Journal:  Cancer        ISSN: 0008-543X            Impact factor:   6.860


  2 in total

1.  Second primary osteosarcoma with rosette-like structure in a patient with retinoblastoma.

Authors:  Kyoji Okada; Tadashi Hasegawa; Ukihide Tateishi; Eiji Itoi
Journal:  Virchows Arch       Date:  2004-07-28       Impact factor: 4.064

2.  Ewing's sarcoma as second malignancy following a short latency in unilateral retinoblastoma.

Authors:  Naveen Tahasildar; Vijay Goni; Kishan Bhagwat; Sujit Kumar Tripathy; Bijnya Birajita Panda
Journal:  J Orthop Traumatol       Date:  2011-08-09
  2 in total

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