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[儿童霍奇金病与自身免疫:11例病例报告]

[Hodgkin disease and autoimmunity in children: 11 case reports].

作者信息

Jarrassé C, Pagnier A, Edan C, Landman-Parker J, Mazingue F, Mansuy L, Bertrand Y, Paillard C, Pellier I, Margueritte G, Plantaz D

机构信息

Service d'oncohématologie pédiatrique, CHU de Grenoble, BP 217, 38043 Grenoble, France.

出版信息

Arch Pediatr. 2011 Apr;18(4):376-82. doi: 10.1016/j.arcped.2011.01.025.

Abstract

The association of lymphoma and autoimmune manifestations has been predominantly studied in adults affected by non-Hodgkin lymphoma. Few publications exist in the literature concerning Hodgkin lymphoma, particularly in children and adolescents. The objectives of this study were to define the characteristics of the link between Hodgkin disease and autoimmunity in childhood. The present 25-year retrospective study was conducted in all centers affiliated with the French Society of Paediatric Oncology (SFCE). Eleven children with Hodgkin disease presented manifestations of disimmunity preceding or following their diagnosis. Four patients had thrombocytopenic purpura, the remaining 7 each had a different autoimmune pathology: lupus syndrome, antiphospholipid syndrome with transient ischemic attack, Evans syndrome, leukocytoclastic vasculitis, autoimmune hemolytic anemia, autoimmune thyroiditis, and juvenile idiopathic arthritis. Lymphoma relapse occurred in 3 patients. Two children died, death being directly attributed to the autoimmune disease in 1 case. Our data suggest that development of autoimmunity is related to significant morbidity. Possible pathophysiological mechanisms include lymphocyte proliferation secondary to chronic inflammation, cell-mediated immune deficiency in Hodgkin disease, molecular mimetics, and antineoplastic phenomena are discussed. A study with a larger patient population is needed to identify the group of children at high risk of autoimmunity for whom additional investigations and modified therapy may be indicated.

摘要

淋巴瘤与自身免疫表现之间的关联主要在非霍奇金淋巴瘤成年患者中进行了研究。关于霍奇金淋巴瘤的文献报道较少,尤其是在儿童和青少年中。本研究的目的是明确儿童期霍奇金病与自身免疫之间联系的特征。本项为期25年的回顾性研究在法国儿科肿瘤学会(SFCE)下属的所有中心开展。11例霍奇金病患儿在诊断之前或之后出现了自身免疫表现。4例患有血小板减少性紫癜,其余7例各有不同的自身免疫性疾病:狼疮综合征、伴有短暂性脑缺血发作的抗磷脂综合征、伊文氏综合征、白细胞破碎性血管炎、自身免疫性溶血性贫血、自身免疫性甲状腺炎和幼年特发性关节炎。3例患者出现淋巴瘤复发。2例患儿死亡,其中1例直接死于自身免疫性疾病。我们的数据表明自身免疫的发生与显著的发病率相关。讨论了可能的病理生理机制,包括慢性炎症继发的淋巴细胞增殖、霍奇金病中的细胞介导免疫缺陷、分子模拟以及抗肿瘤现象。需要开展一项纳入更多患者的研究,以确定自身免疫高风险儿童群体,针对他们可能需要进行额外的检查和调整治疗。

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