A clinical case of manifestation of primary immunodeficiency diagnosed before as Burkitt’s lymphoma

Q4 Medicine
O. Urbas, Z. Vovk, O. A. Holodnykh, U.I. Alekseieva, A.L. Ivanenko
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引用次数: 0

Abstract

Lymphoma is a group of neoplastic diseases characterized by the clonal proliferation of lymphoid cells, manifested by the response of various stages of differentiation of normal B-lymphocytes, less often T-lymphocytes or natural killer cells. The etiology of most lymphomas is unknown. Some of the proven causal-consequence factors are: viral infections and immunodeficiency conditions. Purpose - to draw the attention of non-immunologists to the peculiarities of detecting the primary immunodeficiency (PID) states and the problem of their late diagnosis based on the data of a clinical case. Clinical case. A clinical observation of severe non-genetically differentiated PID is given. Screening signs of PID in the form of recurrent infectious respiratory tract syndrome and frequent long-term use of antibacterial drugs are highlighted, which should alert doctors to clinical and immunological markers of primary immunodeficiency. The presence of Burkitt's lymphoma in the boy also does not exclude the possibility of the manifestation of an immunodeficiency state, both secondary to the drug treatment of lymphoma, and primary, which can manifest itself in puberty. Common variable immunodeficiency is one of those PIDs that "starts" with Burkitt's lymphoma. Conclusions. The problem of low detection of probable PID in children in Ukraine is urgent. Primary care physicians are the first to be able to partially solve this problem by examining the infectious history and laboratory screening tests. There is incomplete awareness of related medical specialties regarding the signs of PID in lymphoproliferative syndrome in children. This clinical case demonstrates signs of PID at an early age. Low detection is also associated with poor capacity and quality and/or lack of immunological laboratory testing, particularly in public facilities. The research was carried out in accordance with the principles of the Helsinki Declaration. The informed consent of the of the child’s parents was obtained for the research No conflict of interests was declared by the authors.
先前诊断为伯基特淋巴瘤的原发性免疫缺陷临床表现1例
淋巴瘤是以淋巴样细胞无性增生为特征的一组肿瘤疾病,表现为正常b淋巴细胞的不同分化阶段的应答,较少出现t淋巴细胞或自然杀伤细胞。大多数淋巴瘤的病因尚不清楚。一些已证实的因果因素是:病毒感染和免疫缺陷状况。目的:根据一个临床病例的数据,引起非免疫学家对原发性免疫缺陷(PID)状态检测的特殊性和后期诊断问题的注意。临床病例。本文对重度非遗传分化型PID进行了临床观察。强调以复发性感染性呼吸道综合征和频繁长期使用抗菌药物为表现形式的PID的筛查征象,应提醒医生注意原发性免疫缺陷的临床和免疫标志物。Burkitt淋巴瘤在男孩身上的存在也不排除免疫缺陷状态表现的可能性,无论是继发于淋巴瘤的药物治疗,还是原发性免疫缺陷状态,都可以在青春期表现出来。常见的可变免疫缺陷是一种从伯基特淋巴瘤开始的免疫缺陷。结论。乌克兰儿童可能的PID检出率低的问题迫在眉睫。初级保健医生是第一个能够通过检查感染史和实验室筛查测试来部分解决这个问题的人。相关医学专业对儿童淋巴细胞增生性综合征的PID体征认识不全。这个临床病例在早期表现出PID的迹象。低检出率还与能力和质量差和/或缺乏免疫学实验室检测有关,特别是在公共设施中。这项研究是按照《赫尔辛基宣言》的原则进行的。本研究获得了儿童父母的知情同意,作者未声明存在利益冲突。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Suchasna pediatriia Ukrayina
Suchasna pediatriia Ukrayina Medicine-Pediatrics, Perinatology and Child Health
CiteScore
0.40
自引率
0.00%
发文量
50
审稿时长
8 weeks
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