INI1 negative hepatoblastoma, a vanishing entity representing malignant rhabdoid tumor
نویسندگان
چکیده
منابع مشابه
Frequent hSNF5/INI1 germline mutations in patients with rhabdoid tumor.
PURPOSE Germline hSNF5/INI1 mutations are responsible for hereditary cases of rhabdoid tumors (RT) that constitute the rhabdoid predisposition syndrome (RPS). Our study provides the first precise overview of the prevalence of RPS within a large cohort of RT. EXPERIMENTAL DESIGN hSNF5/INI1 coding exons were investigated by sequencing and by multiplex ligation-dependent probe amplification. R...
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A 36-month-old girl had a 3-week history of proptosis of the right eye. Computed tomography showed an ill-defined homogeneous mass filling the intraconal space. Histopathologic examination and immunohistochemistry findings of an incisional biopsy specimen were consistent with malignant undifferentiated tumor with rhabdoid features. Despite chemotherapy (a combination of vincristine sulfate and ...
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This is an Open Access article distributed under the terms of the Creative Commons Attribution Non-Commercial License (http://creativecommons.org/licenses/ by-nc/3.0) which permits unrestricted non-commercial use, distribution, and reproduction in any medium, provided the original work is properly cited. Malignant rhabdoid tumors (MRTs) are rare high-grade ma-lignancies in the renal or extraren...
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Malignant rhabdoid tumor is a distinct renal tumor in children. It had been regarded as a rhabdomyosarcomatoid variant of Wilms' tumor, but it is now thought as a separate entity. We report a case of malignant rhabdoid tumor of the kidney in a 26-month-old girl who presented with a left abdominal mass. Grossly, a large mass in the lower pole of the left kidney was well encapsulated and measured...
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ژورنال
عنوان ژورنال: Human Pathology: Case Reports
سال: 2018
ISSN: 2214-3300
DOI: 10.1016/j.ehpc.2018.02.001