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Lymphoproliferative disorders of the orbit: an immunological approach to diagnosis and pathogenesis.

机译:眼眶淋巴增生性疾病:一种诊断和发病机理的免疫学方法。

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摘要

A prospective immunological study of patients with proptosis due to intraorbital lesions composed largely or exclusively of lymphoid tissue indicates that the use of antisera to specific heavy and light chain antibody components can be helpful in distinguishing between polyclonal and truly neoplastic monoclonal disorders. On the basis of combined histological and immunological information it is possible to delineate 4 categories of patient: those with unequivocal chronic inflammation, those with a virtually pure lymphoproliferative lesion and a polyclonal profile, and those with a monoclonal lymphomatous disorder which may be histologically comparable to the previous category or, in a fourth group, be unmistakably malignant on cytological grounds. The first of these groups will normally respond to corticosteroid treatment, but the others, including the polyclonal lymphoproliferative masses, need radiotherapy. The finding of reduced numbers of circulating T cells in the presence of low plasma levels of IgA, and of autoantibodies in the serum of a third of the patients, could mean that individuals developing lymphoproliferative lesions in the orbit, whether hyperplastic or neoplastic, are partially immunodeficient.
机译:对因眶内病变主要或仅由淋巴组织组成的眼眶突出而进行的前瞻性免疫学研究表明,针对特定重链和轻链抗体成分使用抗血清有助于区分多克隆和真正的肿瘤性单克隆疾病。根据组织学和免疫学的综合信息,可以描绘出四类患者:患有明确的慢性炎症的患者,患有真正的单纯淋巴增生性病变和多克隆型的患者以及患有单克隆淋巴瘤性疾病(在组织学上可与之相比)的患者。前一类,或者在第四类中,以细胞学为依据毫无疑问是恶性的。这些组中的第一组通常会对皮质类固醇激素治疗产生反应,但其他组(包括多克隆淋巴增生性肿块)需要放疗。在血浆中IgA水平低的情况下发现循环T细胞数量减少以及三分之一的患者血清中存在自身抗体,这可能意味着在眼眶中发展为增生性或赘生性的淋巴增生性病变的个体部分免疫缺陷。

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