Philadelphia Chromosome Positive Chronic Myelogenous Leukemia Blastic Crisis in a Patient with Unusual Primary Myelofibrosis Characteristics; A Case Report.

Elahe Razmara Lak, Sedigheh Sharifzadeh, Mani Ramzi, Maral Mokhtari, Reza Asadpouri, Elham Abedi, Gholamhossein Tamaddon
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Abstract

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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费城染色体阳性慢性髓性白血病患者的痉挛性危象,具有不寻常的原发性骨髓纤维化特征;病例报告。
导言:骨髓增殖性肿瘤(MPNs)分为BCR-ABL阳性的慢性髓性白血病(CML)和BCR-ABL阴性的MPNs,包括红细胞增多症(PV)、原发性血小板增多症(ET)和原发性骨髓纤维化(PMF)。评估多发性骨髓瘤中的费城染色体是诊断典型 CML 的必要条件:2020 年,一名 37 岁女性被诊断为 CML,其细胞遗传学检测 Janus kinase2(JAK2)、Calreticulin(CALR)、骨髓增生性白血病病毒癌基因(MPL)阴性,BCR-ABL1 突变阳性,骨髓网状纤维化。几年前,患者曾被诊断为 PMF,并伴有组织细胞坏死性淋巴结炎或菊池-藤本氏病(KFD)。最初对 BCR-ABL 融合基因进行了评估,结果呈阴性。随后,皮肤病理学家确诊为皮肤鳞状细胞癌(cSCC),患者可触及脾脏肿大,白细胞(WBC)计数高且伴有嗜碱性粒细胞增多。最后,荧光原位杂交(FISH)和实时定量聚合酶链反应(qRT-PCR)检测出 BCR-ABL 阳性。事实上,PMF与CML是同时存在的:本病例研究强调了一些细胞遗传学方法在多发性骨髓瘤的检测和分类中的重要性。结论:本病例研究强调了一些细胞遗传学方法在多发性骨髓瘤的检测和分类中的重要性,建议医生对此给予更多关注,并在规划治疗时加以注意。
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来源期刊
Cardiovascular and Hematological Agents in Medicinal Chemistry
Cardiovascular and Hematological Agents in Medicinal Chemistry Medicine-Cardiology and Cardiovascular Medicine
CiteScore
2.70
自引率
0.00%
发文量
34
期刊介绍: Cardiovascular & Hematological Agents in Medicinal Chemistry aims to cover all the latest and outstanding developments in medicinal chemistry and rational drug design for the discovery of new Cardiovascular & Hematological Agents. Each issue contains a series of timely in-depth reviews written by leaders in the field covering a range of current topics in Cardiovascular & Hematological medicinal chemistry. Cardiovascular & Hematological Agents in Medicinal Chemistry is an essential journal for every medicinal chemist who wishes to be kept informed and up-to-date with the latest and most important developments in cardiovascular & hematological drug discovery.
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