JAK2阳性骨髓增生异常肿瘤伴纤维化的骨髓肉瘤:病例报告和文献综述。

IF 1.4 4区 医学 Q4 MEDICINE, RESEARCH & EXPERIMENTAL
Jiaofeng Bai, Xuan Wang, Ruirui Zheng, Miao He, Yuexia Zhang, Zhichen Zhang, Xiaolan Yang, Yaozhu Pan
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引用次数: 0

摘要

髓样肉瘤(MS)多发于急性髓性白血病(AML)患者。在极少数情况下,MS可能是骨髓增生性肿瘤(MPN)、骨髓增生异常肿瘤(MDS)或MDS/MPN患者的一种胚泡转化形式。MS最常见的染色体改变是t(8;21)或inv(16),也有其他染色体改变的报道。Janus 激酶 2(JAK2)阳性 MDS 伴纤维化的 MS 病例极为罕见。在此,我们描述了这样一个病例。据我们所知,这是第一例JAK2 V617F突变阳性MDS病例同时伴有累及左侧第七肋骨后方的MS的报道。髓内急性髓细胞性白血病细胞遗传学与髓外疾病发生之间没有明确的关联。有趣的是,该患者髓内 MDS 和髓外肿块的样本出现了相同的 JAK2 V617F 突变。在接受阿扎胞苷和 Venetoclax 治疗方案后,患者的病情得到了完全缓解。胸部 CT 扫描显示,第七根肋骨后肿块消失了。该病例为今后治疗这种疾病提供了宝贵的信息。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Myeloid sarcoma in JAK2-positive myelodysplastic neoplasms with fibrosis: a case report and literature review.

Myeloid sarcoma (MS) occurs in patients with acute myeloid leukemia (AML). In rare cases, MS can represent a form of blast transformation in patients with myeloproliferative neoplasms (MPN), myelodysplastic neoplasms (MDS), or MDS/MPN. The most frequent chromosomal alterations in MS are t(8;21) or inv(16), with other alterations being reported. Cases of MS in Janus kinase 2 (JAK2)-positive MDS with fibrosis are exceedingly rare. Here, we describe such a case. To the best of our knowledge, this is the first report of a JAK2 V617F mutation-positive MDS case occurring concurrently with MS involving the posterior aspect of the left seventh rib. No clear association has been previously demonstrated between the intramedullary AML cytogenetics and extramedullary disease occurrence. Interestingly, samples from the intramedullary MDS and extramedullary mass in this patient presented the same JAK2 V617F mutation. Following a treatment regimen of azacitidine and venetoclax, the patient achieved complete remission. The chest CT scan showed that the seventh posterior rib mass disappeared. This case provides valuable information for the potential future treatment of this disease.

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来源期刊
CiteScore
3.20
自引率
0.00%
发文量
555
审稿时长
1 months
期刊介绍: _Journal of International Medical Research_ is a leading international journal for rapid publication of original medical, pre-clinical and clinical research, reviews, preliminary and pilot studies on a page charge basis. As a service to authors, every article accepted by peer review will be given a full technical edit to make papers as accessible and readable to the international medical community as rapidly as possible. Once the technical edit queries have been answered to the satisfaction of the journal, the paper will be published and made available freely to everyone under a creative commons licence. Symposium proceedings, summaries of presentations or collections of medical, pre-clinical or clinical data on a specific topic are welcome for publication as supplements. Print ISSN: 0300-0605
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