成年患者继发性噬血细胞性淋巴组织细胞病的特点和预后与恶性病因的关系

N. Magy-Bertrand, A. Pastissier, J. Razanamahery, S. Humbert, T. Soumagne, É. Daguindau, C. Chirouze, G. Piton
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引用次数: 0

摘要

成人嗜血球性淋巴组织细胞增多症(HLH)可能继发于癌症或其他疾病。我们的目的是比较成人中继发性HLH的特征和结果,这取决于癌症状态。体重减轻超过10%,头痛和淋巴结肿大在恶性HLH (M-HLH)中更为常见。M-HLH患者存在较高的磷酸酶碱性水平和CRP水平。M-HLH组在第一个月和2年随访期间死亡率有较高的趋势。一些临床特征和生物学异常与成人继发性HLH中恶性肿瘤的可能性增加有关。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Characteristics and Outcomes of Adult Patients with Secondary Hemophagocytic Lymphohistiocytosis Depending on Malignancy Etiology
Hemophagocytic lymphohistiocytosis (HLH) may be secondary to cancer or other conditions in adults. We aimed to compare characteristics and outcomes of secondary HLH depending on cancer status among adults. Weight loss over 10 %, headache and enlarged lymph nodes were more frequent in malignant- HLH (M-HLH). Higher phosphatase alkaline level and CRP level were present in M-HLH. Mortality rate tended to be higher in M-HLH group in the first month and during the two years follow-up. Some clinical features and biological abnormalities are associated with an increased probability of malignancy in secondary HLH among adults.
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