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[1例恶性组织细胞增多症患者高铁蛋白血症的机制]

[Mechanism of hyperferritinemia in a case of malignant histiocytosis].

作者信息

Miyazawa K, Shiota M, Takakuwa Y, Kawanishi Y, Iwabuchi H, Nakano M, Yoshikawa O, Toyama K, Serizawa H, Nagasawa H

机构信息

1st Department of Internal Medicine, Tokyo Medical College.

出版信息

Nihon Ketsueki Gakkai Zasshi. 1990 May;53(3):575-81.

PMID:2386009
Abstract

We report a case of malignant histiocytosis diagnosed by liver-spleen biopsy under laparoscopy. A 49-year-old woman was admitted to our hospital with thrombocytopenia, moderate anemia and hypoproteinemia. Her bone marrow findings revealed erythroid and megakaryocyte hyperplasia, and the serum ferritin concentration was 2,250 ng/ml though she had not received any blood transfusions. Ferrokinetics analysis showed the pattern of ineffective erythropoiesis, and the half-lives of erythrocytes and platelets were both shortened. Her hepatosplenomegaly gradually increased accompanied by increasing serum ferritin level to 10,000 ng/ml. Liver-spleen biopsy was carried out under laparoscopy and revealed infiltration of atypical histiocytes with erythrophagocytosis, which were positive for S-100 and ferritin but negative for lysozyme. The rate of glycosylation in whole serum ferritin, analyzed by using concanavalin-A binding method, showed that her glycosylated ferritin content was only 8.3%, whereas in sera after iron overloading, it was about 70%. Serum isoferritin profiles by isoelectric focussing were studied, and isoferritin pattern from malignant histiocytosis was the same as that in iron overloading after neuraminidase treatment. These findings suggest that serum ferritin is synthesized in proliferating histiocytes and released in the plasma as a nonsecretory type (nonglycosylated ferritin) in this case.

摘要

我们报告一例通过腹腔镜下肝脾活检确诊的恶性组织细胞增多症。一名49岁女性因血小板减少、中度贫血和低蛋白血症入住我院。她的骨髓检查显示红系和巨核细胞增生,尽管未接受任何输血治疗,血清铁蛋白浓度仍为2250 ng/ml。铁动力学分析显示无效红细胞生成模式,红细胞和血小板的半衰期均缩短。她的肝脾肿大逐渐加重,同时血清铁蛋白水平升至10000 ng/ml。在腹腔镜下进行肝脾活检,结果显示有非典型组织细胞浸润并伴有红细胞吞噬现象,这些细胞S-100和铁蛋白呈阳性,但溶菌酶呈阴性。采用伴刀豆球蛋白-A结合法分析全血清铁蛋白的糖基化率,结果显示她的糖基化铁蛋白含量仅为8.3%,而铁过载后血清中的糖基化铁蛋白含量约为70%。通过等电聚焦研究血清异铁蛋白谱,发现恶性组织细胞增多症的异铁蛋白模式与神经氨酸酶处理后的铁过载情况相同。这些发现表明,在该病例中,血清铁蛋白是由增殖的组织细胞合成并以非分泌型(非糖基化铁蛋白)释放到血浆中的。

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