RASGRP1 Deficiency Associated with Diffuse Mesangial Sclerosis Infantile Nephrotic Syndrome and Epstein-Barr Virus-Induced Hodgkin's Lymphoma

被引:0
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作者
Nashrudin, Khairoon Nisa Mohamed [1 ,2 ]
Abidin, Mohd Azri Zainal [1 ,2 ]
Ng, Shi Eng [3 ]
Razali, Hadibiah [4 ]
Jawin, Vida [4 ]
Zakaria, Atiqah Farah [5 ]
Ali, Razana Mohd [6 ]
Othman, Ida Shahnaz [7 ]
Unni, Mohamed Najib Mohamed [7 ]
Hung, Christina Yuh-Ron [8 ]
Ismail, Intan Hakimah [1 ,2 ]
机构
[1] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Paediat, Clin Immunol Unit, Serdang 43400, Selangor, Malaysia
[2] Univ Putra Malaysia, Hosp Sultan Abdul Aziz Shah, Adv Med Res Allergy & Clin Immunol AMRAC, Serdang, Selangor, Malaysia
[3] Hosp Sultan Ismail, Dept Paediat, Johor Baharu, Malaysia
[4] Hosp Sultan Ismail, Paediat Haematooncol Unit, Johor Baharu, Malaysia
[5] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Otorhinolaryngol Head & Neck Surg, Serdang, Selangor, Malaysia
[6] Univ Putra Malaysia, Fac Med & Hlth Sci, Dept Pathol, Serdang, Selangor, Malaysia
[7] Hosp Tunku Azizah, Paediat Haematooncol Unit, Kuala Lumpur, Malaysia
[8] Invitae Corp, San Francisco, CA USA
关键词
RASGRP1; deficiency; Epstein-Barr virus; lymphoproliferation; diffused mesangial sclerosis; nephrotic syndrome; immunodeficiency; IMMUNODEFICIENCY;
D O I
10.1089/ped.2024.0062
中图分类号
R392 [医学免疫学];
学科分类号
100102 ;
摘要
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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页码:11 / 20
页数:10
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