Literature DB >> 11104030

Deletion of Xq23 is a recurrent karyotypic abnormality in acute myeloid leukemia.

K F Wong1, L L Siu, C C So.   

Abstract

Deletion of chromosome Xq23 has been reported in a number of solid tumors, including soft tissue sarcoma, malignant melanoma, astrocytoma, and adenocarcinoma. The deleted Xq often occurs in a setting of very complex karyotypic changes. A similar abnormality has also been described in rare cases of acute myeloid leukemia (AML) but in no other hematologic malignancies. In this study, we report the occurrence of del(X)(q23) in two cases of AML.

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Year:  2000        PMID: 11104030     DOI: 10.1016/s0165-4608(00)00271-5

Source DB:  PubMed          Journal:  Cancer Genet Cytogenet        ISSN: 0165-4608


  2 in total

1.  RABGAP1L gene rearrangement resulting from a der(Y)t(Y;1)(q12;q25) in acute myeloid leukemia arising in a child with Klinefelter syndrome.

Authors:  Maria Cristina Roberti; Roberta La Starza; Cecilia Surace; Pietro Sirleto; Rita Maria Pinto; Valentina Pierini; Barbara Crescenzi; Cristina Mecucci; Adriano Angioni
Journal:  Virchows Arch       Date:  2009-01-28       Impact factor: 4.064

2.  Identification of i(X)(p10) as the sole molecular abnormality in atypical chronic myeloid leukemia evolved into acute myeloid leukemia.

Authors:  Carmelo Gurnari; Paola Panetta; Emiliano Fabiani; Anna Maria Nardone; Diana Postorivo; Giulia Falconi; Luca Franceschini; Manuela Rizzo; Vito Mario Rapisarda; Eleonora De Bellis; Francesco Lo-Coco; Maria Teresa Voso
Journal:  Mol Clin Oncol       Date:  2017-12-29
  2 in total

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