Atlas of Genetics and Cytogenetics in Oncology and Haematology


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t(5;17)(q13;q21)

Clinics and Pathology

Disease T-cell leukemia/lympoma
Epidemiology only 2 cases so far
Clinics a 31 yr old male patient and a 22 yr old female patient with organomegaly
Prognosis insufficient data

Cytogenetics

Additional anomalies complex karyotype in one case; no case yet with the t(5;17) as the sole anomaly

External links

Other databaset(5;17)(q13;q21) Mitelman database (CGAP - NCBI)
Other databaset(5;17)(q13;q21) CancerChromosomes (NCBI)

To be noted

Additional cases are needed to delineate the epidemiology of this rare entity:
you are welcome to submit a paper to our new Case Report section.

Bibliography

17p anomalies in lymphoid malignancies: diagnostic and prognostic implications.
Schoch C, Rieder H, Stollmann-Gibbels B, Freund M, Tischler HJ, Silling-Engelhardt G, Fonatsch C
Leukemia & lymphoma. 1995 ; 17 (3-4) : 271-279.
PMID 8580796
 
Translocation (5;17)(q13;q21) in a case with precursor T-lymphoblastic lymphoma/leukemia.
Zamora L, Espinet B, Solˆ© F, Salido M, Rodon N, Florensa L, Woessner S
Cancer genetics and cytogenetics. 2002 ; 132 (1) : 81-82.
PMID 11801318
 

Contributor(s)

Written02-2002Jean-Loup Huret

Citation

This paper should be referenced as such :
Huret JL . t(5;17)(q13;q21). Atlas Genet Cytogenet Oncol Haematol. February 2002 .
URL : http://AtlasGeneticsOncology.org/Anomalies/t0517ID1210.html

© Atlas of Genetics and Cytogenetics in Oncology and Haematology
indexed on : Mon May 12 18:12:26 2008


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