Literature DB >> 11572252

Rare incidence of three consecutive primary tumors in the maxillofacial region: retinoblastoma, leiomyosarcoma, and choriocarcinoma: case report.

U Márta1, S Zsuzsanna, B József, N Zsolt, S Béla, S György.   

Abstract

Multiple primary tumors occur more commonly in the region of the head and neck than elsewhere in the body. The chance of this is particularly high in patients treated for retinoblastoma, in part because of a genetic predisposition, and in part because of the possibility of irradiation treatment. However, triple tumors occur in only 0.5% of multiple tumors. A rare case of a triple (metachronous) tumor is reported: 12 years after the treatment of bilateral retinoblastoma (enucleation and irradiation), secondary leiomyosarcoma developed in the maxillofacial region, followed 5 years later by choriocarcinoma. Surgery was performed on all three types of tumor. As a result, the female patient (currently 21 years old) is now free of complaints and has married. It is extremely rare for either leiomyosarcoma or choriocarcinoma (CHC) to appear in the maxillofacial region. The long-term, systematic control of such patients is absolutely necessary, for the multiple tumors tend to develop only after a long latency period of 10 to 20 years.

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Year:  2001        PMID: 11572252     DOI: 10.1097/00001665-200109000-00012

Source DB:  PubMed          Journal:  J Craniofac Surg        ISSN: 1049-2275            Impact factor:   1.046


  3 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

2.  Soft tissue, pelvic, and urinary bladder leiomyosarcoma as second neoplasm following hereditary retinoblastoma.

Authors:  L Venkatraman; J R Goepel; K Steele; S P Dobbs; R W Lyness; W G McCluggage
Journal:  J Clin Pathol       Date:  2003-03       Impact factor: 3.411

3.  Intramucosal leiomyosarcoma of the stomach following hereditary retinoblastoma in childhood - a case report and review of the literature.

Authors:  Ursula Pauser; Horst Grimm
Journal:  World J Surg Oncol       Date:  2008-12-14       Impact factor: 2.754

  3 in total

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