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免疫母细胞性淋巴结病(Immunobla-stic Lymphadenopathy),亦称“伴有异常蛋白血症的血管—免疫母细胞性淋巴结病”(AILD)、“淋巴肉芽肿病X”“慢性多源性免疫增生综合征”,是近几年才被确定的一种新的疾病。自1973年Luckes、1974年Frizzera等确认本病以来,引起了临床和病理学者的注意,相继有不少病例报告。近五年来,仅就笔者所查阅到的国外文献中已有132例。国内廖清奎等于1978年报告第一例。可见本病并非罕见。
Immunobla-stic Lymphadenopathy, also known as “AILD” with anaphylactoid disease (AILD), “Lymphatic Granulomatosis X” “Chronic polygenic immunopathies Syndrome ”is a new disease that has only been confirmed in recent years. Since the confirmation of this disease by Luckes in 1973 and Frizzera in 1974, it has attracted the attention of clinicians and pathologists, and many cases have been reported one after another. In the past five years, only 132 foreign documents have been consulted by the author. Domestic Liao Qingkui equals the first case of 1978 report. Shows that the disease is not uncommon.