131
Views
4
CrossRef citations to date
0
Altmetric
Letters to the Editor

Therapy-related myeloid sarcoma with an NPM1 mutation

, , , &
Pages 2130-2131 | Received 03 Jun 2010, Accepted 13 Jul 2010, Published online: 21 Sep 2010

References

  • Falini B, Lenze D, Hasserjian R, et al Cytoplasmic mutated nucleophosmin (NPM) defines the molecular status of a significant fraction of myeloid sarcomas. Leukemia 2007;21:1566–1570.
  • Pileri S, Ascani S, Cox M, et al Myeloid sarcoma: clinico-pathologic, phenotypic, and cytogenetic analysis of 92 adult patients. Leukemia 2007;21:340–350.
  • Andersen MT, Andersen MK, Christiansen DH, et al NPM1 mutations in therapy-related acute myeloid leukemia with uncharacteristic features. Leukemia 2008;22:951–955.
  • Falini B, Nicoletti I, Massimo F, et al Acute myeloid leukemia carrying cytoplasmic/mutated nucleophosmin (NPMc+ AML); biologic and clinical features. Blood 2007;109:874–885.
  • Schnittger S, Schoch C, Kern W, et al Nucleophosmin gene mutations are predictors of favorable prognosis in acute myelogenous leukemia with a normal karyotype. Blood 2005;106:3733–3739.
  • Swerdlow S, Campo E, Harris L, et al WHO classification of tumours of haematopoietic and lymphoid tissues. Lyon: IARC; 2008.
  • Thiede C, Koch S, Creutzig E, et al Prevalence and prognostic impact of NPM1 mutations in 1485 adult patients with acute myeloid leukemia. Blood 2006;107:4011–4020.

Reprints and Corporate Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

To request a reprint or corporate permissions for this article, please click on the relevant link below:

Academic Permissions

Please note: Selecting permissions does not provide access to the full text of the article, please see our help page How do I view content?

Obtain permissions instantly via Rightslink by clicking on the button below:

If you are unable to obtain permissions via Rightslink, please complete and submit this Permissions form. For more information, please visit our Permissions help page.