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淋巴结髓系肉瘤与急性单核细胞性髓系白血病并存:一例报告及文献复习

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

作者信息

Khaja Misbahuddin, Omesh Toolsie, Niazi Masooma, Shaikh Danial, Mudunuru Sitarama Arvind, Reyes Olga Alexandra, Malik Sandeep

机构信息

Division of Pulmonary and Critical Care Medicine, Bronx Care Health System, Affiliated with Icahn School of Medicine at Mount Sinai, Bronx, New York, USA.

Division of Pathology, Bronx Lebanon Hospital Center, Affiliated with Icahn School of Medicine at Mount Sinai, Bronx, New York, USA.

出版信息

Case Rep Oncol. 2018 Nov 29;11(3):791-799. doi: 10.1159/000494830. eCollection 2018 Sep-Dec.

Abstract

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.

摘要

背景

急性髓系白血病(AML)是成人中最常见的白血病。根据法国-美国-英国(FAB)系统,单核细胞白血病被归类为M5。髓系肉瘤在3%至5%的AML患者中进一步发生。它被定义为髓系细胞在淋巴结、软组织、骨膜、骨骼、中枢神经系统(CNS)、脊髓、肠道、纵隔、前列腺、子宫或卵巢中的髓外肿瘤。

病例介绍

在此,我们描述了一名29岁女性的病例,她出现发热、牙龈肿胀、颈部疼痛和乏力,这些症状持续了1周。患者白细胞(WBC)计数为53.5 K/μL,外周血涂片显示髓母细胞(原始细胞)百分比为8%。颈部计算机断层扫描(CT)显示淋巴结病。颈部淋巴结细针穿刺显示有成群的非典型未成熟髓系细胞,混有偶尔的巨核细胞,以及嗜酸性髓系细胞浸润到淋巴结,符合髓系肉瘤。流式细胞术分析显示有中等大小至大的循环原始细胞,核不规则,染色质细腻,核仁明显,提示为AML伴单核细胞分化。患者对氟达拉滨、阿糖胞苷、粒细胞集落刺激因子(G-CSF)和伊达比星化疗反应良好;白细胞计数恢复正常,患者出院回家。

结论

淋巴结髓系肉瘤是AML罕见的伴随病症。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。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7ed7/6323399/acb38d96c488/cro-0011-0791-g01.jpg

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