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[纯红细胞再生障碍性贫血合并胸腺瘤和肺癌:1例报告及文献复习]

[Pure white cell aplasia combined with thymoma and lung cancer: a case report and literature review].

作者信息

Chen X L, Cai Z J, Zheng R, Lin W Q

机构信息

Department of Hematology, the First Hospital of Putian City, Putian 351100, China.

Department of Hematology, the First Hospital of Putian City, Putian 351100, China School of Clinical Medicine, Fujian Medical University, Fuzhou 350000, China.

出版信息

Zhonghua Xue Ye Xue Za Zhi. 2024 Aug 14;45(8):789-793. doi: 10.3760/cma.j.cn121090-20240113-00018.

Abstract

Pure white cell aplasia (PWCA) is a rare hematologic disorder. In this case study, a 67-year-old man presented with severe neutropenia along with thymoma and lung cancer. A comprehensive diagnostic approach was done which included routine blood test, bone marrow cytology, bone marrow pathology, flow cytometry, and thymic pathology. Other potential causes, such as pure red blood cell aplasia and myelodysplastic syndrome, were ruled out. The final diagnosis was determined to be thymoma-related PWCA. Continuous treatment with human granulocyte colony-stimulating factor (G-CSF) was ineffective for treating PWCA in this patient. The patient's white blood cell and neutrophil count increased following treatment with cyclosporine and subsequently returned to normal levels by the 8th day after thymectomy. A recurrence of PWCA was identified 40 days after the operation and coincided with COVID-19 infection. The patient eventually succumbed to a severe infection. Therefore, in cases of severe neutropenia with an unclear etiology, prompt evaluation of mediastinal and bone marrow status is imperative.

摘要

纯白细胞再生障碍(PWCA)是一种罕见的血液系统疾病。在本病例研究中,一名67岁男性出现严重中性粒细胞减少症,同时伴有胸腺瘤和肺癌。采取了综合诊断方法,包括血常规、骨髓细胞学检查、骨髓病理学检查、流式细胞术和胸腺病理学检查。排除了其他潜在病因,如纯红细胞再生障碍和骨髓增生异常综合征。最终诊断为胸腺瘤相关的PWCA。连续使用人粒细胞集落刺激因子(G-CSF)治疗该患者的PWCA无效。患者接受环孢素治疗后白细胞和中性粒细胞计数升高,随后在胸腺切除术后第8天恢复正常水平。术后40天发现PWCA复发,同时合并COVID-19感染。患者最终死于严重感染。因此,对于病因不明的严重中性粒细胞减少症病例,必须及时评估纵隔和骨髓状况。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/ef87/11535556/226819e1b8fd/cjh-45-08-789-g001.jpg

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