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Hemophagocytic syndrome associated with Kikuchis disease.

机译:与菊池病相关的吞噬血细胞综合征。

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摘要

A 13-yr-old female was admitted to our hospital with fever, seizure, and cervical lymphadenopathy. Laboratory data showed pancytopenia, elevation of serum transaminase, lactate dehydrogenase, triglyceride, and ferritin levels. Lymph node biopsy revealed features of Kikuchi's disease and there were signs of histiocytosis and hemophagocytic phenomenon in bone marrow. She recovered after treatment with intravenous immunoglobulin and corticosteroids therapy. Hemophagocytic syndrome can be associated with Kikuchi's disease especially in childhood and seems to have a less aggressive clinical course and better prognosis.
机译:一名13岁的女性因发烧,癫痫发作和宫颈淋巴结肿大入院。实验室数据显示全血细胞减少症,血清转氨酶升高,乳酸脱氢酶,甘油三酸酯和铁蛋白水平。淋巴结活检显示菊池病的特征,骨髓中有组织细胞增多和吞噬细胞现象的迹象。静脉注射免疫球蛋白和糖皮质激素治疗后,她康复了。噬血细胞综合征可能与菊池氏病有关,尤其是在儿童时期,临床病程较轻,预后较好。

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