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Journal Article
12/2010
Sarcomas of the vulva account for only 1-3% of all vulvar malignancies. Most common vulvar sarcomas are leiomyosarcomas, malignant fibrohistiocytomas, and... 
tumors of vulva | Malignant rhabdoid tumor | vulvar sarcomas | malignant extrarenal rhabdoid tumor
Web Resource
Pediatric Blood & Cancer, ISSN 1545-5009, 08/2019, Volume 66, Issue 8, pp. e27784 - n/a
Malignant rhabdoid tumors (MRTs) are rare, highly aggressive embryonal neoplasms caused by biallelic alterations of the SMARCB1 gene. MRTs may occur in any... 
yolk sac tumor | malignant rhabdoid tumor | SMARCB1‐deficient tumor | SNP array analysis | ONCOLOGY | PEDIATRICS | SMARCB1-deficient tumor | COMBINATION | HEMATOLOGY | CHEMOTHERAPY | CHILDREN | Analysis | Tumors | Malignant rhabdoid tumor | Yolk sac | Neoplasms | Soft tissues | Mimicry | Yolk
Journal Article
World Neurosurgery, ISSN 1878-8750, 2016, Volume 85, pp. 197 - 204
Background Atypical teratoid/rhabdoid tumors (AT/RTs) are highly malignant neoplasms that rarely occur in adults. Due to the complex histology of AT/RTs, the... 
Neurosurgery | Brain tumor | Rhabdoid tumor | Clinical management | Pineal tumor | Atypical teratoid/rhabdoid tumor | Genomics | SURGERY | MALIGNANT RHABDOID TUMOR | GLIOMA | ACTIN CYTOSKELETON ORGANIZATION | CLINICAL NEUROLOGY | GLIOBLASTOMA | PLEOMORPHIC XANTHOASTROCYTOMA | CENTRAL-NERVOUS-SYSTEM | OF-THE-LITERATURE | YOUNG-ADULT | A-CASE-REPORT | BRAIN | Pituitary Neoplasms - surgery | Pituitary Neoplasms - diagnosis | Humans | Middle Aged | Teratoma - diagnosis | Male | Rhabdoid Tumor - pathology | Teratoma - surgery | Chemoradiotherapy, Adjuvant | SMARCB1 Protein | DNA Mutational Analysis | Teratoma - radiotherapy | Diagnosis, Differential | Infratentorial Neoplasms - genetics | Rhabdoid Tumor - surgery | Infratentorial Neoplasms - radiotherapy | Pituitary Neoplasms - genetics | Gene Silencing | Rhabdoid Tumor - radiotherapy | Pituitary Neoplasms - pathology | Combined Modality Therapy | Transcription Factors - genetics | DNA-Binding Proteins - genetics | Infratentorial Neoplasms - pathology | Chromosomal Proteins, Non-Histone - genetics | Magnetic Resonance Imaging | Teratoma - pathology | Neurologic Examination | Rhabdoid Tumor - genetics | Biopsy | Genetic Markers - genetics | Brain - pathology | Infratentorial Neoplasms - surgery | Teratoma - genetics | Brain - surgery | Rhabdoid Tumor - diagnosis | Infratentorial Neoplasms - diagnosis | Medical colleges | Adults | Tumors
Journal Article
Child's Nervous System, ISSN 0256-7040, 1/2018, Volume 34, Issue 1, pp. 165 - 167
Rhabdoid tumors are highly malignant tumors predominantly affecting the pediatric population. When these tumors occur outside of the kidneys, they are referred... 
Neurosciences | Malignant extrarenal rhabdoid tumor | Medicine & Public Health | Neurosurgery | Intradural | Lumbar | Pediatric | MERT | Sacral | SURGERY | SPINE | PEDIATRICS | CLINICAL NEUROLOGY
Journal Article
Pediatric and Developmental Pathology, ISSN 1093-5266, 6/2017, Volume 20, Issue 3, pp. 262 - 266
Introduction Malignant rhabdoid tumor (MRT) is defined as a high-grade sarcoma derived from an uncertain cell of origin. Its diagnosis is associated with poor... 
Malignant rhabdoid tumor | Soft tissue tumor | Oncology | Sarcoma | Pediatric | SMARCB1/INI1 | SURVIVAL | sarcoma | PATHOLOGY | oncology | pediatric | CHILDREN | INI1 | malignant rhabdoid tumor | SARCOMAS | PEDIATRICS | MUTATIONS | EXPRESSION | soft tissue tumor
Journal Article
Modern Pathology, ISSN 0893-3952, 09/2018, Volume 31, Issue 9, pp. 1442 - 1456
Small cell carcinoma of the ovary, hypercalcemic type is a rare, aggressive malignancy which usually occurs in young women and is characterized by mutations in... 
OVARY | SMALL-CELL-CARCINOMA | MIXED MULLERIAN TUMOR | ATYPICAL TERATOID/RHABDOID TUMOR | HYPERCALCEMIC TYPE | SMARCA4 MUTATIONS | PATHOLOGY | OF-THE-LITERATURE | EXPRESSION | ENDOMETRIOID ADENOCARCINOMA | INI1 GENE | Malignant rhabdoid tumor | Sarcoma | Ovariectomy | Cytology | Malignancy | Hysterectomy | Ovaries | Cervix | Hypercalcemia | Uterus | Morphology | Mutation | Uterine cancer | Endometrium | Tumors
Journal Article