| Literature DB >> 20048688 |
Anwar Al Nassan1, Maher Sughayer, Ismail Matalka, Khalil Ghandour, Main Masarweh, Arthur Zimmermann, Iyad Sultan.
Abstract
Malignant rhabdoid tumor (MRT) of the liver is a rare malignancy with grave prognosis. This entity should be considered in the differential diagnosis of any aggressive liver tumor with low levels of alpha fetoprotein. We report 2 cases of hepatic MRT presenting in infancy. In these 2 cases, we show that loss of INI1 facilitates making the correct diagnosis of primary hepatic MRT utilizing BAF 47 (INI1 gene product) immunostains. Difficulty encountered in making this rare diagnosis, including the need for repeated biopsies, can be avoided if MRT is considered in the differential diagnosis early on and BAF 47 immunohistochemistry is ordered.Entities:
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Year: 2010 PMID: 20048688 DOI: 10.1097/MPH.0b013e3181b79613
Source DB: PubMed Journal: J Pediatr Hematol Oncol ISSN: 1077-4114 Impact factor: 1.289