A Novel Case of Extreme Thrombocytosis in Acute Myeloid Leukemia Associated With Isochromosome 17q and Copy Neutral Loss of Heterozygosity-Reference-Cited by-同舟云学术

A Novel Case of Extreme Thrombocytosis in Acute Myeloid Leukemia Associated With Isochromosome 17q and Copy Neutral Loss of Heterozygosity

Published:2015-05-01 Issue:3 Volume:35 Page:366-369
ISSN:2234-3806
Container-title:Annals of Laboratory Medicine
language:en
Short-container-title:Ann Lab Med

Author:

You Eunkyoung¹²,Cho Sun Young²,Yang John Jeongseok²,Lee Hee Joo²,Lee Woo-In²,Lee Juhie³,Cho Kyung Sam⁴,Cho Eun Hae⁵,Park Tae Sung²

Affiliation:

1. Department of Medicine, Graduate School, Kyung Hee University, Seoul, Korea

2. Departments of Laboratory Medicine, School of Medicine, Kyung Hee University, Seoul, Korea

3. Departments of Pathology, School of Medicine, Kyung Hee University, Seoul, Korea

4. Departments of Hematology-Oncology, School of Medicine, Kyung Hee University, Seoul, Korea

5. Green Cross Genome, Yongin, Korea

Funder

Kyung Hee University

Publisher

Annals of Laboratory Medicine

Subject

Biochemistry, medical,Clinical Biochemistry,General Medicine

Link

https://synapse.koreamed.org/pdf/10.3343/alm.2015.35.3.366

Reference9 articles.

1. Isochromosome 17q in Blast Crisis of Chronic Myeloid Leukemia and in Other Hematologic Malignancies Is the Result of Clustered Breakpoints in 17p11 and Is Not Associated With Coding TP53 Mutations

2. Isochromosomes in neoplasia

3. Myeloid neoplasms with isolated isochromosome 17q represent a clinicopathologic entity associated with myelodysplastic/myeloproliferative features, a high risk of leukemic transformation, and wild-type TP53

4. Acute myeloid leukemia associated with t(1;3)(p36;q21) and extreme thrombocytosis: a clinical study with literature review

5. t(1;3)(p36;q21). Atlas Genet Cytogenet Oncol Haematol. 2002. Last accessed on May 18, 2010. Available at: http://AtlasGeneticsOncology.org/Anomalies/t0103.html

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