Lukina E A, Levina A A, Mokeeva R A
All-Union Scientific Centre for Haematology, Moscow, Russia.
Br J Haematol. 1993 Feb;83(2):326-9. doi: 10.1111/j.1365-2141.1993.tb08289.x.
Iron metabolism was studied in 10 patients with malignant histiocytosis (MH), in 16 patients with histiocytosis-X (Langerhans cell histiocytosis) and in 34 patients with reactive proliferation of the mononuclear phagocytes (MPS). Eight MH patients had a considerably increased level of serum ferritin (SF). The average level of SF was 6070 +/- 957 mg/l for MH patients, which is significantly greater than the SF level for HX and RH patients. The study of the serum ferritin profiles suggests that the main pathogenetic mechanism of hyperferritinaemia in MH is the synthesis and secretion of ferritin by neoplastic mononuclear phagocytes. From this, hyperferritinaemia in MH may be considered as pathognomic of this disease and used as an additional diagnostic criterion. In addition, SF is the most informative parameter for the clinical practice among the indices of the functional state of MPS.
对10例恶性组织细胞增多症(MH)患者、16例组织细胞增多症-X(朗格汉斯细胞组织细胞增多症)患者和34例单核吞噬细胞反应性增生(MPS)患者的铁代谢进行了研究。8例MH患者血清铁蛋白(SF)水平显著升高。MH患者的SF平均水平为6070±957mg/l,明显高于HX和RH患者的SF水平。血清铁蛋白谱研究表明,MH患者高铁蛋白血症的主要发病机制是肿瘤性单核吞噬细胞合成和分泌铁蛋白。由此可见,MH患者的高铁蛋白血症可被视为该疾病的特征,并用作额外的诊断标准。此外,在MPS功能状态指标中,SF是临床实践中最具信息价值的参数。