Literature DB >> 18521207

The location and appearance of second malignancies in patients with bilateral retinoblastoma.

C Z Rubin1, N S Rosenfield, S J Abramson, D H Abramson, I J Dunkel.   

Abstract

Purpose. This paper describes the clinical history and radiographic appearance of second malignancies in patients with bilateral retinoblastoma.Subjects/methods. The imaging studies and clinical data of 14 patients with a history of bilateral retinoblastoma who were treated for second malignancies were reviewed.Results. A total of 17 tumors were identified in 14 patients during the period 1978-1996. The median age of occurrence of the second malignancy was 17 years (range 10-32 years). Fourteen of the 17 malignancies occurred in the facial structures and three developed in the lower extremities. The histologies included osteosarcoma (n = 5), malignant fibrous histiocytoma (n = 3), high-grade spindle cell sarcoma (n = 3), malignant mesenchymoma (n = 1), leiomyosarcoma (n = 4) and angiosarcoma (n = 1). The tumors were locally aggressive and had a similar appearance to those found in nonretinoblastoma patients. Six of the 14 patients are alive and disease free.Discussion. Most of the adolescent and young adult retinoblastoma survivors developed second malignancies in the irradiated facial structures but some occurred in distal sites. Radiologically, these tumors do not differ in appearance from those seen in non-retinoblastoma patients with the exception of their location.

Entities:  

Year:  1997        PMID: 18521207      PMCID: PMC2395350          DOI: 10.1080/13577149778353

Source DB:  PubMed          Journal:  Sarcoma        ISSN: 1357-714X


  11 in total

1.  CHROMOSOME DELETION IN A CASE OF RETINOBLASTOMA.

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3.  Radiation induced neoplasia following external beam therapy for children with retinoblastoma.

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5.  The surgical management of retinoblastoma.

Authors:  D H Abramson; R M Ellsworth
Journal:  Ophthalmic Surg       Date:  1980-09

6.  Mortality from second tumors among long-term survivors of retinoblastoma.

Authors:  C Eng; F P Li; D H Abramson; R M Ellsworth; F L Wong; M B Goldman; J Seddon; N Tarbell; J D Boice
Journal:  J Natl Cancer Inst       Date:  1993-07-21       Impact factor: 13.506

7.  Second nonocular tumors in retinoblastoma survivors. Are they radiation-induced?

Authors:  D H Abramson; R M Ellsworth; F D Kitchin; G Tung
Journal:  Ophthalmology       Date:  1984-11       Impact factor: 12.079

8.  Osteosarcoma and retinoblastoma: a shared chromosomal mechanism revealing recessive predisposition.

Authors:  M F Hansen; A Koufos; B L Gallie; R A Phillips; O Fodstad; A Brøgger; T Gedde-Dahl; W K Cavenee
Journal:  Proc Natl Acad Sci U S A       Date:  1985-09       Impact factor: 11.205

9.  Incidence of second primary tumours among childhood cancer survivors.

Authors:  M M Hawkins; G J Draper; J E Kingston
Journal:  Br J Cancer       Date:  1987-09       Impact factor: 7.640

10.  Patterns of multiple primary tumours in patients treated for cancer during childhood.

Authors:  J E Kingston; M M Hawkins; G J Draper; H B Marsden; L M Kinnier Wilson
Journal:  Br J Cancer       Date:  1987-09       Impact factor: 7.640

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  2 in total

1.  Nasal sinus leiomyosarcoma in a patient with history of non-hereditary unilateral treated retinoblastoma.

Authors:  Sarah G Fitzpatrick; Bradford A Woodworth; Carmela Monteiro; Raafat Makary
Journal:  Head Neck Pathol       Date:  2010-08-29

Review 2.  Leiomyosarcoma of the Nasal Cavity and Paranasal Sinuses: A Case Report and Comprehensive Review of the Literature.

Authors:  Sumita S Sam; Brian Stewart; Elham Nasri; Marino E Leon; Ernesto Martinez Duarte
Journal:  Head Neck Pathol       Date:  2022-02-14
  2 in total

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