HOMEPRODUCTSCOMPANYCONTACTFAQResearchDictionaryPharmaSign Up FREE or Login

Concurrent acute myeloid leukemia with inv(16)(p13.1q22) and chronic lymphocytic leukemia: molecular evidence of two separate diseases.

Abstract
Acute myeloid leukemia (AML) occurring concurrently with or after untreated chronic lymphocytic leukemia (CLL) is rare. We report a case of a 59-year-old man who was evaluated for anemia, thrombocytopenia, and leukocytosis with circulating blasts. On the basis of the morphology and immunophenotyping results, a preliminary diagnosis of chronic myelomonocytic leukemia with concurrent CLL was considered. Subsequently, cytogenetic analysis of the leukemic blood specimen revealed inv(16)(p13.1q22) with secondary trisomy 22 in a sideline clone. Fluorescence in situ hybridization confirmed the CBFbeta rearrangement associated with inv(16) in myeloblasts and myelomonocytic cells, but not in CLL cells. Therefore, a final diagnosis of AML with inv(16) with concurrent CLL was made. After standard chemotherapy for AML, the patient achieved complete remission for both his AML and CLL. The unique aspects of this case include concomitant AML and CLL, which do not share clonality, complex cytogenetic abnormalities with trisomy 22 as a secondary abnormality associated with inv(16), and achievement of remission for both AML and CLL by AML chemotherapy regimen. This case also represents one of the rare instances where a diagnosis of AML can be established even when the blast percentage in the marrow and blood is less than 20%.
AuthorsChuanyi M Lu, Joyce L Murata-Collins, Endi Wang, Imran Siddiqi, H Jeffrey Lawrence
JournalAmerican journal of hematology (Am J Hematol) Vol. 81 Issue 12 Pg. 963-8 (Dec 2006) ISSN: 0361-8609 [Print] United States
PMID16917916 (Publication Type: Case Reports, Journal Article)
Topics
  • Blast Crisis (diagnosis, drug therapy, genetics, pathology)
  • Bone Marrow (pathology)
  • Chromosome Inversion (genetics)
  • Chromosomes, Human, Pair 16 (genetics)
  • Chromosomes, Human, Pair 22 (genetics)
  • Humans
  • In Situ Hybridization, Fluorescence (methods)
  • Leukemia, Lymphocytic, Chronic, B-Cell (diagnosis, drug therapy, genetics, pathology)
  • Leukemia, Myeloid, Acute (diagnosis, drug therapy, genetics, pathology)
  • Male
  • Middle Aged
  • Neoplasms, Second Primary (diagnosis, drug therapy, genetics, pathology)
  • Remission Induction
  • Trisomy (genetics)

Join CureHunter, for free Research Interface BASIC access!

Take advantage of free CureHunter research engine access to explore the best drug and treatment options for any disease. Find out why thousands of doctors, pharma researchers and patient activists around the world use CureHunter every day.
Realize the full power of the drug-disease research graph!


Choose Username:
Email:
Password:
Verify Password:
Enter Code Shown: