Hodgkin lymphoma in patient with primary immunodeficiency: clinical features and treatment approaches

Author:

Utesheva K. I.1ORCID,Belyaeva E. S.1ORCID,Valiev T. T.2ORCID,Odzharova A. A.1ORCID

Affiliation:

1. N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia

2. N.N. Blokhin National Medical Research Center of Oncology, Ministry of Health of Russia; I.M. Sechenov First Moscow State Medical University, Ministry of Health of Russia (Sechenov University)

Abstract

Primary immunodeficiencies (PID) are genetically determined irreversible disorders of structure and/or functions of the immune system's cellular and humoral components, accompanied by frequent infectious diseases and contributing to the development of malignant neoplasms. Lymphomas are the most frequent oncological disease in PID patients: non-Hodgkin's lymphomas occur in 60 % of malignant neoplasms cases, Hodgkin lymphoma - in 20 %, leukemias - in 10 %, solid tumors - in 10 %. The risk of malignant lymphoproliferative diseases in PID patients amounts to 4-25 %, with the overall incidence of cancer 100-200 times higher than in immunocompetent population. Results of malignant neoplasms treatment in children with PID remain unsatisfactory due to the high rate of relapsed, refractory disease and anticancer therapy complications.This paper presents a clinical case of Hodgkin lymphoma with atypical localization in a female PID patient. peculiarities of this case are eye socket soft tissue involvement, slow response to therapy, and a high rate of infectious complications.

Publisher

Publishing House ABV Press

Subject

Oncology,Hematology

Reference7 articles.

1. Mueller B.U., Pizzo P.A. Cancer in children with primary or secondary immunodeficiencies. J Pediatr 1995;126(1):1-10.

2. Ochs H.D., Hitzig W.H. History of primary immunodeficiency diseases. Curr Opin Allergy Clin Immunol 2012;12(6):577-87. DOI: 10.1097/ACI.0b013e32835923a6

3. Tran H., Nourse J., Hall S. et al. Immunodeficiencyassociated lymphomas. Blood Rev 2008;22(5):261-81.

4. Ярилин А.А. Иммунология. М.: ГЭОТАР-Медиа, 2010. 749 с. [Yarilin A.A. Immunology. Moscow: GEOTAR-Media, 2010. 749 p. (In Russ.)].

5. Saar K., Chrzanowska K.H., Stumm M. et al. The gene for the ataxia-telangiectasia variant, Nijmegen breakage syndrome, aps to a 1-cM interval on chromosome 8q21. Am J Hum Genet 1997;60:605-10.

同舟云学术

1.学者识别学者识别

2.学术分析学术分析

3.人才评估人才评估

"同舟云学术"是以全球学者为主线,采集、加工和组织学术论文而形成的新型学术文献查询和分析系统,可以对全球学者进行文献检索和人才价值评估。用户可以通过关注某些学科领域的顶尖人物而持续追踪该领域的学科进展和研究前沿。经过近期的数据扩容,当前同舟云学术共收录了国内外主流学术期刊6万余种,收集的期刊论文及会议论文总量共计约1.5亿篇,并以每天添加12000余篇中外论文的速度递增。我们也可以为用户提供个性化、定制化的学者数据。欢迎来电咨询!咨询电话:010-8811{复制后删除}0370

www.globalauthorid.com

TOP

Copyright © 2019-2024 北京同舟云网络信息技术有限公司
京公网安备11010802033243号  京ICP备18003416号-3