个案报道和文献复习:同胞兄弟同时感染微小病毒B19致纯红细胞再生障碍性贫血
A Case Report and Review of the Literature: Pure Red Cell Aplasia Occurs in Two Brothers Caused by Infected with Parvovirus B19
摘要: 目的:本研究报道了同胞兄弟二人因贫血症状就诊,均诊断为微小病毒B19致纯红细胞再生障碍性贫血,旨在提高对微小病毒B19感染特点的了解,尤其是提高其对造血系统影响的认识。方法:回顾性分析1例微小病毒B19感染致纯红细胞再生障碍性贫血的临床资料,对患者进行人微小病毒B19 (DNA)定量检测、骨髓穿刺等检查,同时查阅文献进行总结分析。本病例报道已获得病人家属的知情同意。结果:患者临床表现为发热、乏力,血常规以贫血为主要表现,白细胞偏低,微小病毒B19 (DNA)定量检测结果显示拷贝数较高,IgM抗体阳性,骨髓提示红系比例极低。结论:同胞兄弟二人同时感染微小病毒B19致纯红细胞再生障碍性贫血较为少见。病毒DNA检测及IgM抗体检查,并结合骨髓结果,可明确诊断,治疗无需特殊处理,部分需应用大剂量静注人免疫球蛋白冲击,预后相对较好。
Abstract: Objective: In this study, we reported a case of pure red cell aplasia caused by parvovirus B19 in two brothers with anemia, in order to improve the understanding of the characteristics of parvovirus B19 infection, especially its effect on hematopoietic system. Methods: The clinical data of the case of pure red cell aplasia caused by parvovirus B19 infection were retrospectively analyzed. The patients were examined by quantitative detection of human parvovirus B19 (DNA), Bone Marrow Examination, etc. At the same time, the literature is summarized and analyzed. This case report has obtained the informed consent from the patient’s family. Results: The clinical manifestations of patients were fever, and hypodynamia. Blood analysis suggests anemia and leukopenia. Quantitative detection of parvovirus B19 (DNA) indicated a high copy number and IgM antibody was positive. And bone marrow indicates a very low percentage of erythroids. Conclusion: It is rare that two brothers got pure red cell aplasia at the same time because of infecting with parvovirus B19. It can be diagnosed through viral DNA detection, IgM antibody examination, and Bone Marrow Examination. The treatment is normal, but some patients should use large doses of intravenous immunoglobulins. All patients had achieved good curative effect.
文章引用:杨洁, 王瑞仓, 杨永宾, 李杰, 袁军, 李燕, 郝洪岭. 个案报道和文献复习:同胞兄弟同时感染微小病毒B19致纯红细胞再生障碍性贫血[J]. 临床医学进展, 2019, 9(11): 1328-1333. https://doi.org/10.12677/ACM.2019.911205

参考文献

[1] 李增庆, 黄咏梅, 乔福元, 等. 巢式PCR检测人微小病毒B19非结构蛋白DNA的应用价值[J]. 华中科技大学学报(医学版), 2004, 33(4): 412-415.
[2] Kinney, J.S., Andemon, L.J., Farrar, J., et al. (1998) Risk of Adverse Out-comes of Pregnancy after Human Parvovirus B19 Infection. The Journal of Infectious Diseases, 157, 663-667. [Google Scholar] [CrossRef] [PubMed]
[3] Bonsch, C., Zuercher, C., Lieby, P., et al. (2010) The Globoside Re-ceptor Triggers Structural Changes in the B19 Virus Capsid That Facilitate Virus Internalization. Journal of Virology, 84, 11737-11746. [Google Scholar] [CrossRef
[4] Heegaard, E.D. and Brown, K.E. (2002) Human Parvovirus B19. Clin-ical Microbiology Reviews, 15, 485-505. [Google Scholar] [CrossRef
[5] Kerr, J.R. (2015) A Review of Blood Diseases and Cytope-nias Associated with Human Parvovirus B19 Infection. Reviews in Medical Virology, 25, 224-240. [Google Scholar] [CrossRef] [PubMed]
[6] Brown, K.E., Hibbs, J.R., Galinela, G., et al. (1994) Resistance to Parvovi-rus B19 Infection Due to Lack of Virus Receptor (Erythrocyte P Antigen). The New England Journal of Medicine, 330, 1192-1196. [Google Scholar] [CrossRef
[7] Mofat, S., Yaegashi, N., Tada, K., et al. (1998) Human Parvovirus B19 Nonstructural (NS1) Protein Induces Apoptosis in Erythroid Lineage Cells. Journal of Virology, 72, 3018-3028.
[8] Young, N.S. (1996) Parvovirus Infection and Its Treatment. Clinical & Experimental Immunology, 104, 26-30. [Google Scholar] [CrossRef
[9] 陈朝晖, 张宏艳. 人类微小病毒B19致小儿心脏损害15例临床分析[J]. 临床荟萃, 2007, 22(16): 1176-1177.
[10] Abdolahi, A., Shoar, S., Sheikhbahaei, S., et al. (2014) Status of Immunity against PVB19 in HIV-Infected Patients According to CD4(+) Cell Count, and Antiretroviral Therapy Regi-men Groups. Nigerian Medical Journal, 55, 20-23. [Google Scholar] [CrossRef] [PubMed]
[11] Hirokawa, M. (2016) Progress in the Clinical Management of Pure Red Cell Aplasia and Future Prospects. Rinsho Ketsueki, 57, 110-116.
[12] 李栋林, 梁廷波. 实体器官移植后纯红细胞再生障碍性贫血的病因与诊治[J]. 中华医学杂志, 2006, 86(42): 3020-3022.
[13] Staley, E.M., Schwartz, J. and Pham, H.P. (2016) An Update on ABO Incompatible Hematopoietic Progenitor Cell Transplantation. Transfusion and Apheresis Science, 54, 337-344. [Google Scholar] [CrossRef] [PubMed]
[14] Mouthon, L., Guillevin, L. and Tellier, Z. (2005) Intravenous Immunoglobulins in Autoimmune or Parvovirus B19-Mediated Pure Red-Cell Aplasia. Autoimmunity Reviews, 4, 264-269. [Google Scholar] [CrossRef] [PubMed]
[15] Uik, N., Miyamura, T., Obama, K., Takahira, H., Sato, H. and Kozuru, M. (1993) Parvovirus B19-Associated Haemophagocytosis in Evans Syndrome: A Plastic Crisis Accompanied by Severe Thrombocytopenia. British Journal of Haematology, 84, 530-532. [Google Scholar] [CrossRef] [PubMed]
[16] Sekiguchi, Y., Shimada, A., Imai, H., Wakabayashi, M., Sugimoto, K., Nakamura, N., Sawada, T., Komatsu, N. and Noguchi, M. (2014) A Case of Recurrent Autoimmune He-molytic Anemia during Remission Associated with Acute Pure Red Cell Aplasia and Hemophagocytic Syndrome Due to Human Parvovirus B19 Infection Successfully Treated by Steroid Pulse Therapy with a Review of the Literature. Inter-national Journal of Clinical and Experimental Pathology, 7, 2624-2635.
[17] Puigví, L., Baumann, T., Fernández, S., Castro, P., Pereira, A. and Merino, A. (2017) Massive Erythrophagocytosis by Peripheral Monocytes and Neutrophils in Parvovirus-B19 Autoimmune Hemolytic Anemia. Annals of Hematology, 96, 881-882. [Google Scholar] [CrossRef] [PubMed]
[18] Bihari, C., Rastogi, A. and Saxenaetal, P. (2013) Parvovirus B19 Associated Hepatitis. Hepatitis Research and Treatment, 2013, Article ID: 472027.
[19] Furukawa, M., Kaji, K., Ma-suda, H., Ozaki, K. and Asada, S. (2017) Severe Aplastic Anemia Following Parvovirus B19-Associated Acute Hepatitis. Case Reports in Hepatology, 2017, Article ID: 1359486. [Google Scholar] [CrossRef] [PubMed]