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胸腺瘤中的副肿瘤综合征:免疫学视角

Paraneoplastic syndromes in thymoma: an immunological perspective.

作者信息

Nelson Robert P, Pascuzzi Robert M

机构信息

Division of Hematology and Oncology, Indiana University School of Medicine, Indianapolis, IN, USA.

出版信息

Curr Treat Options Oncol. 2008 Dec;9(4-6):269-76. doi: 10.1007/s11864-008-0081-1. Epub 2009 Feb 6.

Abstract

T lymphocyte development occurs primarily during fetal life through cell-to-cell interactions with epithelial and dendritic cells. Evidence now supports the concept that thymic function continues during adulthood, which may explain why thymic neoplasms are associated with immunodeficiency and autoimmune illness. A broad variety of autoimmune conditions are observed in patients with thymic tumors, especially hematological and paraneurological syndromes, including aplastic anemia, pure red cell aplasia and myasthenia gravies, encephalomyelitis, cerebellar degeneration, sensory neuropathies, and Lambert-Eaton myasthenic syndrome. A more thorough understanding of the immunological dysfunction in patients with thymoma and thymic carcinoma promises to contribute to the overall understanding of human immunology and improve the clinical management of patients.

摘要

T淋巴细胞的发育主要发生在胎儿期,通过与上皮细胞和树突状细胞的细胞间相互作用实现。目前有证据支持胸腺功能在成年期仍持续存在的观点,这或许可以解释为什么胸腺肿瘤与免疫缺陷和自身免疫性疾病相关。胸腺肿瘤患者会出现各种各样的自身免疫性病症,尤其是血液学和副神经学综合征,包括再生障碍性贫血、纯红细胞再生障碍和重症肌无力、脑脊髓炎、小脑变性、感觉神经病变以及兰伯特-伊顿肌无力综合征。对胸腺瘤和胸腺癌患者免疫功能障碍的更深入了解,有望促进对人类免疫学的全面认识,并改善患者的临床管理。

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