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Print ISSN: 1792-1074 Online ISSN: 1792-1082
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September-2015 Volume 10 Issue 3

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Case Report

Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report

  • Authors:
    • Qian Wu
    • Bo Xiao
    • Li Li
    • Li Feng
  • View Affiliations / Copyright

    Affiliations: Department of Neurology, Xiangya Hospital, Central South University, Changsha, Hunan 410008, P.R. China
  • Pages: 1561-1564
    |
    Published online on: June 17, 2015
       https://doi.org/10.3892/ol.2015.3389
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Abstract

Atypical teratoid/rhabdoid tumor (AT/RT) is an aggressive embryonic brain tumor that is predominantly found in young children. The present study reports the unusual case of an adult male AT/RT patient with a history of another type of tumor, hereditary multiple exostoses (EXT or HME), who survived for 18 years. The patient's first and chief complaint was a 1‑month history of progressive projectile vomiting. The patient was admitted twice for treatment, and on the second admission, a craniotomy was performed to remove a intracranial mass. However, no radiotherapy or chemotherapy treatment was administered. Pathology revealed monotonous medium‑ to large‑sized neoplastic cells. The patient succumbed to a pulmonary infection and respiratory failure 14 days after the initial treatment. The prognosis for AT/RT is extremely poor; furthermore, the patient presented with another tumor. There may have been an association between the two tumors that worsened the clinical phenotype and prognosis of this patient. Additionally, symptomatic treatment for this condition is insufficient; early surgery and radiotherapy may be more useful for preventing the aggressive progression of these tumors.
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Copy and paste a formatted citation
Spandidos Publications style
Wu Q, Xiao B, Li L and Feng L: Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report. Oncol Lett 10: 1561-1564, 2015.
APA
Wu, Q., Xiao, B., Li, L., & Feng, L. (2015). Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report. Oncology Letters, 10, 1561-1564. https://doi.org/10.3892/ol.2015.3389
MLA
Wu, Q., Xiao, B., Li, L., Feng, L."Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report". Oncology Letters 10.3 (2015): 1561-1564.
Chicago
Wu, Q., Xiao, B., Li, L., Feng, L."Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report". Oncology Letters 10, no. 3 (2015): 1561-1564. https://doi.org/10.3892/ol.2015.3389
Copy and paste a formatted citation
x
Spandidos Publications style
Wu Q, Xiao B, Li L and Feng L: Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report. Oncol Lett 10: 1561-1564, 2015.
APA
Wu, Q., Xiao, B., Li, L., & Feng, L. (2015). Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report. Oncology Letters, 10, 1561-1564. https://doi.org/10.3892/ol.2015.3389
MLA
Wu, Q., Xiao, B., Li, L., Feng, L."Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report". Oncology Letters 10.3 (2015): 1561-1564.
Chicago
Wu, Q., Xiao, B., Li, L., Feng, L."Atypical teratoid/rhabdoid tumor with hereditary multiple exostoses in an 18-year-old male: A case report". Oncology Letters 10, no. 3 (2015): 1561-1564. https://doi.org/10.3892/ol.2015.3389
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