scholarly journals Case Analysis of 14 Children with Malignant Rhabdoid Tumor of the Kidney

2021 ◽  
Vol Volume 13 ◽  
pp. 4865-4872
Author(s):  
Jing Li ◽  
Weiling Zhang ◽  
Huimin Hu ◽  
Yi Zhang ◽  
Yizhuo Wang ◽  
...  
Keyword(s):  
Case Analysis ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor

Congenital Cerebellar Malignant Rhabdoid Tumor in an Infant With Junctional Epidermolysis Bullosa

2006 ◽  
Vol preprint (2007) ◽  
pp. 1
Author(s):  
Henry Krous ◽  
Amy Chadwick ◽  
Elisabeth Haas ◽  
Eric Breisch ◽  
Homeyra Masoumi
Keyword(s):  
Epidermolysis Bullosa ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor ◽  
Junctional Epidermolysis Bullosa

MALIGNANT RHABDOID TUMOR MIMICKING HEPATOBLASTOMA: A CASE REPORT AND LITERATURE REVIEW

2006 ◽  
Vol preprint (2007) ◽  
pp. 1
Author(s):  
Lars Wagner ◽  
Jennifer Garrett ◽  
Edgard Ballard ◽  
D. Hill ◽  
Arie Perry ◽  
...  
Keyword(s):  
Case Report ◽  
Literature Review ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor

Epithelioid Sarcoma Arising in a Long-Term Survivor of an Atypical Teratoid/Rhabdoid Tumor in a Patient With Rhabdoid Tumor Predisposition Syndrome

2021 ◽  
pp. 109352662098649
Author(s):  
Tiffany G Baker ◽  
Michael J Lyons ◽  
Lee Leddy ◽  
David M Parham ◽  
Cynthia T Welsh
Keyword(s):  
Epithelioid Sarcoma ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor ◽  
Atypical Teratoid Rhabdoid Tumor ◽  
Diagnostic Challenge ◽  
Patient Demographics ◽  
Immunohistochemical Markers ◽  
Genetic Aberration ◽  
Atypical Teratoid ◽  
Rhabdoid Tumors

Rhabdoid tumor predisposition syndrome (RTPS) is defined as the presence of a SMARCB1 or SMARCA4 genetic aberration in a patient with malignant rhabdoid tumor. Patients with RTPS are more likely to present with synchronous or metachronous rhabdoid tumors. Based on the current state of rhabdoid tumor taxonomy, these diagnoses are based largely on patient demographics, anatomic location of disease, and immunohistochemistry, despite their nearly identical histologic and immunohistochemical profiles. Thus, the true distinction between such tumors remains a diagnostic challenge. Central nervous system atypical teratoid/rhabdoid tumor (AT/RT) is a rare, aggressive, primarily pediatric malignancy with variable histologic features and a well documented association with loss of SMARCB1 expression. Epithelioid sarcoma (ES) is a rare soft tissue tumor arising in patients of all ages and characteristically staining for both mesenchymal and epithelial immunohistochemical markers while usually demonstrating loss of SMARCB1 expression. To our knowledge we herein present the first documented case of a patient with RTPS who presented with metachronous AT/RT and ES.

scholarly journals Malignant rhabdoid tumor—The great mimicker: Two case reports

2021 ◽  
Vol 16 (4) ◽  
pp. 815-818
Author(s):  
Dasic Ivana ◽  
Cvejic Sofija ◽  
Pavicevic Polina ◽  
Rancic Smilja
Keyword(s):  
Case Reports ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor

scholarly journals Malignant rhabdoid tumor of the bladder and ganglioglioma in a 14 year-old male with a germline 22q11.2 deletion

2014 ◽  
Vol 207 (9) ◽  
pp. 415-419 ◽  
Author(s):  
Kristopher R. Bosse ◽  
Aseem R. Shukla ◽  
Bruce Pawel ◽  
Kudakwashe R. Chikwava ◽  
Mariarita Santi ◽  
...  
Keyword(s):  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor ◽  
22Q11.2 Deletion

scholarly journals Malignant Rhabdoid Tumor of the Lung in the Young Adult: A Case Report

2011 ◽  
Vol 2011 ◽  
pp. 1-4 ◽  
Author(s):  
Adel Attia ◽  
Moosa Suleman ◽  
Hesham Mosleh
Keyword(s):  
Case Report ◽  
Young Adult ◽  
Pediatric Oncology ◽  
Wilms Tumor ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor

Malignant rhabdoid tumor (MRT) is one of the most aggressive and lethal malignancies in pediatric oncology. Malignant rhabdoid tumor was initially described in 1978 as a rhabdomyosarcomatoid variant of a Wilms tumor because of its occurrence in the kidney and because of the resemblance of its cells to rhabdomyoblasts. The absence of muscular differentiation led Haas and colleagues to coin the term rhabdoid tumor of the kidney in 1981, Haas et al..

INI1 expression induces cell cycle arrest and markers of senescence in malignant rhabdoid tumor cells

2003 ◽  
Vol 194 (3) ◽  
pp. 303-313 ◽  
Author(s):  
Britta S. Reincke ◽  
Gary B. Rosson ◽  
Betty W. Oswald ◽  
Cynthia F. Wright
Keyword(s):  
Cell Cycle ◽  
Cell Cycle Arrest ◽  
Tumor Cells ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor ◽  
Cycle Arrest

Treatment of Stage IV Malignant Rhabdoid Tumor of the Kidney (MRTK) With ICE and VDCy

2006 ◽  
Vol 28 (5) ◽  
pp. 286-289 ◽  
Author(s):  
Masaki Yamamoto ◽  
Nobuhiro Suzuki ◽  
Naoki Hatakeyama ◽  
Nobuo Mizue ◽  
Tsukasa Hori ◽  
...  
Keyword(s):  
Stage Iv ◽  
Rhabdoid Tumor ◽  
Malignant Rhabdoid Tumor
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