Ewing Sarcoma with 7;22 translocation: Three new cases and clinicopathological characterization

Fetal and Pediatric Pathology

Volumn 31, Issue 6, 2012, Pages 341-348

  Shulman, Sarah Catherine ^a   Katzenstein, Howard ^b   Bridge, Julia ^c   Bannister, Lucas L ^a   Qayed, Muna ^b   Oskouei, Shervin ^d   Shehata, Bahig M ^a  

^a Children's Healthcare of Atlanta ^*  (United States)

^b CHILDREN'S HEALTHCARE OF ATLANTA   (United States)

^c UNIVERSITY OF NEBRASKA MEDICAL CENTER   (United States)

^d EMORY UNIVERSITY SCHOOL OF MEDICINE   (United States)

Author keywords

Ewing sarcoma (ES); T(7; 22); Translocation

Indexed keywords

TRANSCRIPTION FACTOR; TRANSCRIPTION FACTOR ER81; TRANSCRIPTION FACTOR ERG; TRANSCRIPTION FACTOR ETS; TRANSCRIPTION FACTOR ETV4; TRANSCRIPTION FACTOR FEV; TRANSCRIPTION FACTOR FLI 1; UNCLASSIFIED DRUG;

AGE DISTRIBUTION; ARTICLE; CASE REPORT; CHILD; CHROMOSOME 22; CHROMOSOME 7; CLINICAL ASSESSMENT; EWING SARCOMA; FEMALE; FLUORESCENCE IN SITU HYBRIDIZATION; HIGH RISK POPULATION; HISTOPATHOLOGY; HUMAN; INFANT; KARYOTYPING; PRIORITY JOURNAL; SCHOOL CHILD; SEX DIFFERENCE; SYSTEMATIC REVIEW;

ABNORMAL KARYOTYPE; BONE NEOPLASMS; CHILD; CHROMOSOMES, HUMAN, PAIR 22; CHROMOSOMES, HUMAN, PAIR 7; COMBINED MODALITY THERAPY; DISEASE-FREE SURVIVAL; DNA, NEOPLASM; FATAL OUTCOME; FEMALE; HUMANS; IN SITU HYBRIDIZATION, FLUORESCENCE; INFANT; ONCOGENE PROTEINS, FUSION; SARCOMA, EWING; TRANSLOCATION, GENETIC; TUMOR MARKERS, BIOLOGICAL;

EID: 84867728037     PISSN: 15513815     EISSN: 15513823     Source Type: Journal    
DOI: 10.3109/15513815.2012.659397     Document Type: Article

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