[纯合子白细胞增生症合并胸腺瘤和肺癌:病例报告和文献综述]。

X L Chen, Z J Cai, R Zheng, W Q Lin
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引用次数: 0

摘要

纯合子白细胞增生症(PWCA)是一种罕见的血液病。在本病例研究中,一名 67 岁的男子出现了严重的中性粒细胞减少症,并伴有胸腺瘤和肺癌。对他进行了全面的诊断,包括血常规检查、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,如纯红细胞增生症和骨髓增生异常综合征。最终确诊为胸腺瘤相关的 PWCA。持续使用人粒细胞集落刺激因子(G-CSF)治疗该患者的PWCA无效。使用环孢素治疗后,患者的白细胞和中性粒细胞计数增加,随后在胸腺切除术后第 8 天恢复到正常水平。术后 40 天,PWCA 复发,并伴有 COVID-19 感染。患者最终死于严重感染。因此,在病因不明的重症中性粒细胞减少症病例中,必须及时评估纵隔和骨髓状况。
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[Pure white cell aplasia combined with thymoma and lung cancer: a case report and literature review].

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.

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CiteScore
0.80
自引率
0.00%
发文量
100
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