2006
DOI: 10.1002/ajh.20716
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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 tr… Show more

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Cited by 17 publications
(12 citation statements)
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“…Our cases support the idea that AML and CLL might demonstrate two separate disease processes, which is CLL originates from abnormal CD5+CD19 positive lymphoid clone whereas AML originates from myeloid from CD34, CD117, CD13, CD33, and MPO positive myeloid clone. Lu CM et al showed that in a patient AML and CLL developed from different clones [13]. We only showed immunophenotypic features of AML and CLL were different.…”
Section: Discussionmentioning
confidence: 52%
“…Our cases support the idea that AML and CLL might demonstrate two separate disease processes, which is CLL originates from abnormal CD5+CD19 positive lymphoid clone whereas AML originates from myeloid from CD34, CD117, CD13, CD33, and MPO positive myeloid clone. Lu CM et al showed that in a patient AML and CLL developed from different clones [13]. We only showed immunophenotypic features of AML and CLL were different.…”
Section: Discussionmentioning
confidence: 52%
“…Therapy-related acute monoblastic leukemia (M5) in CLL, as in the present case, has rarely been reported [Lavabre-Bertrand et al 1989]. Our review of previously published cases demonstrates that AML and CLL may be diagnosed concurrently or after a variable latency period (<2-13 years) [Bracey et al 1989;Robertson et al 1994;Mateu et al 1997;Meloni et al 2000;Molero et al 2001;Lam et al 2005;Lu et al 2006;Hatoum et al 2007;Park et al 2009]. Rarely, the development of AML may not manifest with peripheral circulating blasts [Robertson et al 1994].…”
Section: Discussionmentioning
confidence: 58%
“…The present patient did not have any high-risk genetic mutations, however, overt DIC may reflect the aggressive disease manifestation. A few cases with normal karyotype or good-risk cytogenetics such as t(15;17) or inv(16) have also been reported [Molero et al 2001;Lu et al 2006;Hatoum et al 2007]. Unlike the majority of patients, who have poor outcomes [Bracey et al 1989;Robertson et al 1994;Mateu et al 1997], patients with good-risk cytogenetics may have good outcomes [Molero et al 2001;Lu et al 2006;Hatoum et al 2007;Park et al 2009].…”
Section: Discussionmentioning
confidence: 99%
“…18,19 Postoje i hipoteze da ove bolesti nastaju istodobno iz istog klona matične stanice ili je, pak, riječ o dva odvojena procesa. 7,15,[19][20][21][22][23][24] Istodobno prisutni KLL i MDS dijagnostički su izazov. U bolesnika s KLL-om i citopenijom treba pomišljati i na istodobno prisutan MDS.…”
Section: Raspravaunclassified