论文部分内容阅读
坏死性淋巴结炎是由藤本等以非独立性疾患的综合征于1972年报告的。在病理上是以淋巴结副皮质区肿胀,特异性坏死灶,无多核白细胞浸润为特征。此后,相继出现过同样的报告,迄今为止已被确立为一个独立的疾患。可是在小儿科,关于本病的临床、预后等了解不多,而其病因亦尚不明确。病例患儿女,12岁1个月。大约在1980年5月,无特殊诱因即开始发热,颈部左侧淋巴结肿大,
Necrotizing lymphadenitis was reported in 1972 by Fujimoto et al as a syndrome of non-independent disorders. Pathologically based on the paraneoplastic lymph node swelling, specific necrosis, non-multicellular leukocyte infiltration is characterized. Since then, the same report has appeared one after another, so far has been established as an independent disease. However, in pediatrics, about the clinical, prognosis of the disease to understand, and its etiology is not yet clear. Cases of children, 12-year-old for 1 month. About May 1980, no special incentive to start fever, neck lymph nodes on the left,