| Literature DB >> 22082606 |
Jodi M Carter1, Carolyn O'Hara, George Dundas, Dawna Gilchrist, Mark S Collins, Katherine Eaton, Alexander R Judkins, Jaclyn A Biegel, Andrew L Folpe.
Abstract
Epithelioid malignant peripheral nerve sheath tumors arising in preexisting schwannomas are extremely rare. We report an unusual example occurring in a patient with multiple schwannomas (schwannomatosis), all but 1 of which showed "neuroblastoma-like" histology. By immunohistochemistry, both the epithelioid malignant peripheral nerve sheath tumor and the schwannomas showed a complete loss of the Smarcb1 protein. Subsequent genetic evaluation revealed the presence of a novel germline mutation in the SMARCB1/INI1 gene in the patient and in 3 of her children, 2 of whom were diagnosed with atypical teratoid/rhabdoid tumors of the brain.Entities:
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Year: 2012 PMID: 22082606 PMCID: PMC3241826 DOI: 10.1097/PAS.0b013e3182380802
Source DB: PubMed Journal: Am J Surg Pathol ISSN: 0147-5185 Impact factor: 6.394