Atypical teratoid and rhabdoid tumor. Report of a congenital case;Tumeur rhabdoïde et tératoïde atypique. À propos d'un cas congénital

Annales de Pathologie

Volumn 21, Issue 3, 2001, Pages 259-262

  Fernandez, ^a   Sévenet, Nicolas ^b   Bouvier Labit, Corinne ^a   Lena, Gabriel ^a   Figarella Branger, Dominique ^a  

^a TIMONE HOSPITAL   (France)

^b INSTITUT CURIE   (France)

Author keywords

Atypical teratoid and rhabdoid tumor; Cerebral tumor; Congenital; hSNF5 INII gene

Indexed keywords

ALPHA ACTIN; EPITHELIAL MEMBRANE ANTIGEN; VIMENTIN;

ARTICLE; BRAIN TUMOR; CASE REPORT; FACIAL NERVE PARALYSIS; GENE MUTATION; GENETIC ANALYSIS; HETEROZYGOSITY; HOMOZYGOSITY; HUMAN; IMMUNOREACTIVITY; NEUROECTODERM TUMOR; RHABDOID TUMOR; SCHOOL CHILD; TERATOMA; TUMOR LOCALIZATION;

ACTINS; BRAIN NEOPLASMS; CA-15-3 ANTIGEN; CHILD; DNA, NEOPLASM; HUMANS; IMMUNOHISTOCHEMISTRY; MALE; MUTATION; NEOPLASMS, MULTIPLE PRIMARY; NEUROECTODERMAL TUMORS, PRIMITIVE; RHABDOID TUMOR; TERATOMA; VIMENTIN;

EID: 18144450003     PISSN: 02426498     EISSN: None     Source Type: Journal    
DOI: None     Document Type: Article

References (10)

1. Central nervous system atypical teratoid/rhabdoid tumors of infancy and childhood: Definition of an entity
2. Characterization of a primary central nervous system atypical teratoid/rhabdoid tumor and derivated cell line: Immunophenotype and neoplastic properties
3. Atypical teratoid/rhabdoid tumor of the central nervous system: A highly malignant tumor of infancy and childhood frequently mistaken for medulloblastoma
4. Primary congenital rhabdoid tumor of the brain with neoplastic hydranencephaly
5. Monosomy 22 in rhabdoid or atypical tumors of the brain
6. Congenital disseminated malignant rhabdoid tumor. A distinct clinicopathological entity demonstrating abnormalities of chromosome 22q11
7. Truncating mutations of hSNF5/INII in aggressive paediatric cancer
8. Constitutional mutations of the hSNF5/INII gene predispose to a variety of cancers
9. Familial posterior fossa brain tumors of infancy secondary to germline mutation of the hSNF5 gene
10. Tumeur indifférenciée des tissus mous avec phénotype rhabdoïde (tumeur rhabdoïde extra-rénale). À propos d'un cas congénital associé à un médulloblastome dans la fratrie