File Download

There are no files associated with this item.

  Links for fulltext
     (May Require Subscription)
Supplementary

Article: Bone marrow transplantation for therapy-related acute myeloid leukemia in congenital retinoblastoma associated with 13q deletion syndrome

TitleBone marrow transplantation for therapy-related acute myeloid leukemia in congenital retinoblastoma associated with 13q deletion syndrome
Authors
KeywordsAML
Deletion 13q
Marrow transplantation
Retinoblastoma
Issue Date2004
PublisherSpringer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00277/index.htm
Citation
Annals Of Hematology, 2004, v. 83 n. 7, p. 481-483 How to Cite?
AbstractChildren with constitutional deletion of the long arm of chromosome 13 are at risk for retinoblastoma (RB) due to loss of the RB tumor suppressor gene. The prognosis is poor since the tumors are often bilateral, aggressive, and recurrent and the patients often harbor other congenital abnormalities. One further complication is that of therapy-related malignancies later in life. We report a case of allogeneic stem cell transplantation for therapy-related acute myeloid leukemia in an 8-year-old girl after multimodality treatment for refractory bilateral relapsing RB, with excellent outcome in both the ophthalmic and marrow disease. © Springer-Verlag 2004.
Persistent Identifierhttp://hdl.handle.net/10722/79851
ISSN
2021 Impact Factor: 4.030
2020 SCImago Journal Rankings: 1.079
ISI Accession Number ID
References

 

DC FieldValueLanguage
dc.contributor.authorHon, Cen_HK
dc.contributor.authorChan, GCFen_HK
dc.contributor.authorHa, SYen_HK
dc.contributor.authorMa, SKen_HK
dc.contributor.authorWong, KFen_HK
dc.contributor.authorAu, WYen_HK
dc.date.accessioned2010-09-06T07:59:28Z-
dc.date.available2010-09-06T07:59:28Z-
dc.date.issued2004en_HK
dc.identifier.citationAnnals Of Hematology, 2004, v. 83 n. 7, p. 481-483en_HK
dc.identifier.issn0939-5555en_HK
dc.identifier.urihttp://hdl.handle.net/10722/79851-
dc.description.abstractChildren with constitutional deletion of the long arm of chromosome 13 are at risk for retinoblastoma (RB) due to loss of the RB tumor suppressor gene. The prognosis is poor since the tumors are often bilateral, aggressive, and recurrent and the patients often harbor other congenital abnormalities. One further complication is that of therapy-related malignancies later in life. We report a case of allogeneic stem cell transplantation for therapy-related acute myeloid leukemia in an 8-year-old girl after multimodality treatment for refractory bilateral relapsing RB, with excellent outcome in both the ophthalmic and marrow disease. © Springer-Verlag 2004.en_HK
dc.languageengen_HK
dc.publisherSpringer Verlag. The Journal's web site is located at http://link.springer.de/link/service/journals/00277/index.htmen_HK
dc.relation.ispartofAnnals of Hematologyen_HK
dc.subjectAMLen_HK
dc.subjectDeletion 13qen_HK
dc.subjectMarrow transplantationen_HK
dc.subjectRetinoblastomaen_HK
dc.titleBone marrow transplantation for therapy-related acute myeloid leukemia in congenital retinoblastoma associated with 13q deletion syndromeen_HK
dc.typeArticleen_HK
dc.identifier.openurlhttp://library.hku.hk:4550/resserv?sid=HKU:IR&issn=0939-5555&volume=83&spage=481&epage=483&date=2004&atitle=Bone+marrow+transplantation+for+therapy-related+acute+myeloid+leukemia+in+congenital+retinoblastoma+associated+with+13q+deletion+syndromeen_HK
dc.identifier.emailChan, GCF:gcfchan@hkucc.hku.hken_HK
dc.identifier.authorityChan, GCF=rp00431en_HK
dc.description.naturelink_to_subscribed_fulltext-
dc.identifier.doi10.1007/s00277-004-0884-5en_HK
dc.identifier.pmid15170522-
dc.identifier.scopuseid_2-s2.0-3042771623en_HK
dc.identifier.hkuros88935en_HK
dc.relation.referenceshttp://www.scopus.com/mlt/select.url?eid=2-s2.0-3042771623&selection=ref&src=s&origin=recordpageen_HK
dc.identifier.volume83en_HK
dc.identifier.issue7en_HK
dc.identifier.spage481en_HK
dc.identifier.epage483en_HK
dc.identifier.isiWOS:000221733000017-
dc.publisher.placeGermanyen_HK
dc.identifier.scopusauthoridHon, C=7003617146en_HK
dc.identifier.scopusauthoridChan, GCF=16160154400en_HK
dc.identifier.scopusauthoridHa, SY=7202501115en_HK
dc.identifier.scopusauthoridMa, SK=37020910400en_HK
dc.identifier.scopusauthoridWong, KF=37096553800en_HK
dc.identifier.scopusauthoridAu, WY=7202383089en_HK
dc.identifier.issnl0939-5555-

Export via OAI-PMH Interface in XML Formats


OR


Export to Other Non-XML Formats