Atypical teratoid/rhabdoid tumor with retained INI1 (SMARCB1) expression and loss of BRG1 (SMARCA4)
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作者:
Bookhout, Christine
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Univ N Carolina, Dept Surg Pathol, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Surg Pathol, Chapel Hill, NC 27599 USA
Bookhout, Christine
[1
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Bouldin, Thomas W.
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Univ N Carolina, Dept Surg Pathol, Chapel Hill, NC 27599 USAUniv N Carolina, Dept Surg Pathol, Chapel Hill, NC 27599 USA
Bouldin, Thomas W.
[1
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Ellison, David W.
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St Jude Childrens Res Hosp, Dept Neuropathol, 332 N Lauderdale St, Memphis, TN 38105 USAUniv N Carolina, Dept Surg Pathol, Chapel Hill, NC 27599 USA
Ellison, David W.
[2
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机构:
[1] Univ N Carolina, Dept Surg Pathol, Chapel Hill, NC 27599 USA
[2] St Jude Childrens Res Hosp, Dept Neuropathol, 332 N Lauderdale St, Memphis, TN 38105 USA
Atypical teratoid/rhabdoid tumor (AT/RT) is a rare, highly aggressive malignancy of the central nervous system (CNS) usually diagnosed in infancy or childhood, most often characterized by loss of expression of the SMARCB1 gene product integrase interactor 1 (INI1) protein. We report a case of AT/RT in a 3month old boy with retained expression of INI1 by immunohistochemistry. Additional testing demonstrated loss of expression of the SMARCA4 gene product Brahma-related gene 1 (BRG1) protein by immunohistochemistry, confirmed by next generation sequencing showing a nonsense mutation in SMARCA4. This case illustrates that positivity for INI1 does not rule out a diagnosis of AT/RT, and additional testing, including BRG1/SMARCA4 analysis, is warranted in cases where clinical suspicion is high.
机构:
Childrens Hosp Los Angeles, Dept Pathol & Lab Med, Los Angeles, CA USA
Univ So Calif, Keck Sch Med, Los Angeles, CA 90033 USAUniv Hosp Munster, Inst Neuropathol, D-48129 Munster, Germany