...
首页> 外文期刊>Case Reports in Oncology >Co-Occurrence of Myeloid Sarcoma of the Lymph Node and Acute Monocytic Myeloid Leukemia: A Case Report and Literature Review
【24h】

Co-Occurrence of Myeloid Sarcoma of the Lymph Node and Acute Monocytic Myeloid Leukemia: A Case Report and Literature Review

机译:淋巴结髓样肉瘤与急性单核细胞样髓性白血病共存:一例并文献复习

获取原文
   

获取外文期刊封面封底 >>

       

摘要

Background: Acute myeloid leukemia (AML) is the most common leukemia in adults. According to the French-American-British (FAB) system, monocytic leukemia is classified as M5. Myeloid sarcoma further occurs in 3–5% of AML. This is defined as an extramedullary tumor of myeloid cells in the lymph nodes, soft tissues, periosteum, bone, central nervous system (CNS), spinal cord, intestine, mediastinum, prostate, uterus, or ovaries. Case Presentation: Here, we describe the case of a 29-year-old female who presented with fever, swelling of gums, neck pain, and weakness, which had persisted for 1 week. The patient had a white blood cell (WBC) count of 53.5 K/μL, and a peripheral smear revealed a myeloid blast cell (blast) percentage of 8%. Computed tomography (CT) of the neck indicated lymphadenopathy. Fine needle aspiration of the cervical lymph node showed groups of atypical immature myeloid cells, mixed with occasional megakaryocytes, and infiltration of eosinophilic myeloid cells into the lymph node, consistent with myeloid sarcoma. Flow cytometry analysis revealed intermediate to large circulating blasts, with irregular nuclei, fine chromatin, and distinct nucleoli, indicative of AML, with monocytic differentiation. The patient responded well to chemotherapy with fludarabine, cytarabine, granulocyte colony stimulating factor (G-CSF), and idarubicin; WBC counts returned to normal and patient was discharged to home. Conclusion: Myeloid sarcoma of the lymph node is a rare co-occurrence with AML. Results of our study are consistent with the conclusion that early diagnosis and appropriate treatment improve survival.
机译:背景:急性髓细胞白血病(AML)是成人中最常见的白血病。根据法国-美国-英国(FAB)系统,单核细胞白血病被分类为M5。髓样肉瘤在AML的3–5%中进一步发生。这定义为淋巴结,软组织,骨膜,骨骼,中枢神经系统(CNS),脊髓,肠,纵隔,前列腺,子宫或卵巢中的髓样细胞的髓外肿瘤。病例介绍:在这里,我们描述了一个持续发热1周,发烧,牙龈肿胀,颈部疼痛和无力的29岁女性的病例。该患者的白细胞(WBC)计数为53.5 K /μL,外周涂片显示髓样母细胞(blast)的百分比为8%。颈部计算机断层扫描(CT)提示淋巴结肿大。宫颈淋巴结的细针抽吸显示非典型的未成熟骨髓细胞群,与偶尔的巨核细胞混合,嗜酸性粒细胞浸润到淋巴结中,与髓样肉瘤一致。流式细胞仪分析显示,中,大型循环母细胞具有不规则的核,染色质细和核仁,表明是AML,具有单核细胞分化。患者对氟达拉滨,阿糖胞苷,粒细胞集落刺激因子(G-CSF)和伊达比星的化疗反应良好。 WBC计数恢复正常,患者出院回家。结论:淋巴结髓样肉瘤与AML罕见并存。我们的研究结果与早期诊断和适当治疗可提高生存率的结论一致。

著录项

相似文献

  • 外文文献
  • 中文文献
  • 专利
获取原文

客服邮箱:kefu@zhangqiaokeyan.com

京公网安备:11010802029741号 ICP备案号:京ICP备15016152号-6 六维联合信息科技 (北京) 有限公司©版权所有
  • 客服微信

  • 服务号