骨髓纤维化
原发性血小板增多症
真性红细胞增多症
医学
费城染色体
慢性粒细胞白血病
髓系白血病
荧光原位杂交
断点群集区域
白血病
病理
骨髓
内科学
癌症研究
肿瘤科
染色体易位
染色体
生物
生物化学
受体
基因
作者
Elahe Razmara lak,Sedigheh Sharifzadeh,Mani Ramzi,Maral Mokhtari,Reza Asadpouri,Elham Abedi,Gholamhossein Tamaddon
出处
期刊:Cardiovascular and Hematological Agents in Medicinal Chemistry
[Bentham Science Publishers]
日期:2023-06-15
卷期号:22 (2): 240-245
标识
DOI:10.2174/1871525721666230614110621
摘要
Introduction: Myeloproliferative neoplasms (MPNs) are divided into BCR-ABL positive Chronic myeloid leukemia (CML) and BCR-ABL negative MPNs including Polycythemia vera (PV), Essential Thrombocythemia (ET) and Primary myelofibrosis (PMF). Evaluation of the Philadelphia chromosome in MPNs is a diagnostic requirement for classic CML. Case Report: In 2020, a 37-year-old woman with negative cytogenetic testing for Janus kinase2 (JAK2), Calreticulin (CALR), myeloproliferative leukemia virus oncogene (MPL), and positive for BCR-ABL1 mutation with reticular fibrosis in bone marrow was diagnosed as CML. Some years ago, the patient had been diagnosed with PMF with evidence of histiocytic necrotizing lymphadenitis or Kikuchi-Fujimoto disease (KFD). The BCR-ABL fusion gene was initially evaluated which was negative. Then, Cutaneous squamous cell carcinoma (cSCC) was confirmed by Dermatopathologist with palpable splenomegaly and high white blood cell (WBC) count with basophilia. Finally, BCR-ABL was detected positive by the fluorescence in situ hybridization (FISH) and quantitative real-time polymerase chain reaction (qRT-PCR). In fact, the co-occurrence of PMF with CML was identified. Conclusion: This case study highlighted the importance of some cytogenetic methods in the detection and classification of MPNs. It is recommended that physicians pay more attention to it and be aware of the planning treatment.
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