RASGRP1缺失与弥漫性系膜硬化、婴儿肾病综合征和eb病毒诱导的霍奇金淋巴瘤相关

IF 1.1 4区 医学 Q4 ALLERGY
Khairoon Nisa Mohamed Nashrudin, Mohd Azri Zainal Abidin, Shi Eng Ng, Hadibiah Razali, Vida Jawin, Atiqah Farah Zakaria, Razana Mohd Ali, Ida Shahnaz Othman, Mohamed Najib Mohamed Unni, Christina Yuh-Ron Hung, Intan Hakimah Ismail
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引用次数: 0

摘要

背景:RAS鸟苷释放蛋白1 (RASGRP1)缺乏以免疫失调和eb病毒相关淋巴细胞增生为特征。弥漫性系膜硬化是婴儿肾病综合征的罕见病因之一。病例介绍:在这里,我们描述了一个7岁的女孩,她在5个月大时被诊断为弥漫性系膜硬化,随后在3岁时发展为慢性双侧颈部肿胀。临床评估和调查显示了一个复杂的临床情况,包括复发性宫颈淋巴结病和复发性感染。进一步的评估显示免疫缺陷,自身免疫性淋巴增生性综合征样疾病,慢性EBV感染,最终霍奇金淋巴瘤。基因检测发现了一个RASGRP1纯合子功能缺失变异,父母双方都是携带者。结论:这是马来西亚首次报道的RASGRP1缺乏病例,我们强调了当疾病表现为不同表现时临床医生面临的挑战。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
RASGRP1 Deficiency Associated with Diffuse Mesangial Sclerosis Infantile Nephrotic Syndrome and Epstein-Barr Virus-Induced Hodgkin's Lymphoma.

Background: RAS guanyl-releasing protein 1 (RASGRP1) deficiency is characterized by immune dysregulation and Epstein-Barr virus (EBV)-related lymphoproliferation. Diffuse mesangial sclerosis is one of the infrequent causes of infantile nephrotic syndrome. Case Presentation: Here, we described a 7-year-old girl who was diagnosed with diffuse mesangial sclerosis at 5 months old and subsequently developed chronic bilateral neck swelling at the age of 3 years. Clinical assessment and investigations revealed a complex clinical picture, including recurrent cervical lymphadenopathy and recurrent infections. Further evaluation revealed immunological deficiencies, autoimmune lymphoproliferative syndrome-like illness, chronic EBV infection, and ultimately Hodgkin lymphoma. Genetic testing identified a RASGRP1 homozygous loss-of-function variant with both parents being carriers. Conclusion: This is the first reported case of RASGRP1 deficiency in Malaysia, and we highlight the challenges clinicians face when the disease manifests in varied presentations.

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来源期刊
CiteScore
2.00
自引率
0.00%
发文量
23
审稿时长
>12 weeks
期刊介绍: Pediatric Allergy, Immunology, and Pulmonology is a peer-reviewed journal designed to promote understanding and advance the treatment of respiratory, allergic, and immunologic diseases in children. The Journal delivers original translational, clinical, and epidemiologic research on the most common chronic illnesses of children—asthma and allergies—as well as many less common and rare diseases. It emphasizes the developmental implications of the morphological, physiological, pharmacological, and sociological components of these problems, as well as the impact of disease processes on families. Pediatric Allergy, Immunology, and Pulmonology coverage includes: -Functional and genetic immune deficiencies- Interstitial lung diseases- Both common and rare respiratory, allergic, and immunologic diseases- Patient care- Patient education research- Public health policy- International health studies
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