Atypical Teratoid Rhabdoid Tumor of the Cauda Equina in a Child

Report of a Very Unusual Case

James M. Shiflett, Betty L. Herrington, David A. Joyner, Ali Saad

Research output: Contribution to journalArticle

Abstract

Atypical teratoid/rhabdoid tumors (AT/RT) are highly aggressive malignant primitive neoplasms that commonly occur in children younger than 2 years of age. The prognosis is generally dismal with a median survival time of <1 year. The majority of AT/RT occur in the posterior fossa and less frequently the supratentorium. Primary pediatric spinal AT/RT are exceedingly rare and only 15 cases have been reported to date. Here we report a very unusual case of primary spinal AT/RT extensively involving the spinal cord from T11 down to the cauda equina. In this patient, the tumor was highly aggressive and resulted in extensive dissemination into the nerve roots and paraspinal soft tissue rapidly resulting in the patient’s death 1 month after diagnosis. to the best of our knowledge, this degree of involvement of the spine by a primary AT/RT has not been described before.

Original languageEnglish (US)
JournalApplied Immunohistochemistry and Molecular Morphology
DOIs
StateAccepted/In press - Jan 16 2018
Externally publishedYes

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Cauda Equina
Neoplasms
Spinal Cord
Spine
Atypical Teratoid Tumor
Typical Teratoid Rhabdoid Tumor
Pediatrics
Survival

All Science Journal Classification (ASJC) codes

  • Pathology and Forensic Medicine
  • Histology
  • Medical Laboratory Technology

Cite this

Atypical Teratoid Rhabdoid Tumor of the Cauda Equina in a Child : Report of a Very Unusual Case. / Shiflett, James M.; Herrington, Betty L.; Joyner, David A.; Saad, Ali.

In: Applied Immunohistochemistry and Molecular Morphology, 16.01.2018.

Research output: Contribution to journalArticle

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