[Erythrocytic and immunologic abnormalities in myeloid splenomegaly].

C Dao, J L Harousseau, C de Carbonniéres, J Bousser, G Bilski-Pasquier
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Abstract

Screening for red cell defects, and exploration of cellular and humoral immunity has been performed in 33 patients : 31 had agnogenic myelosclerosis with myeloid metaplasia, 3 had polycythemia vera with secondary myelosclerosis. No patient had the biological abnormalities characteristical of paroxysmal nocturnal hemoglobinuria (Marchiafava-Micheli). In 19 out of 21 cases, red cells had antigen i on their membrane, thus suggesting that splenic erythropoiesis could give rise to immature erythrocytes. Two patients had a monoclonal dysglobulinemia, 5 a positive Coombs test, 6 a rhumatoid factor in the serum, 3 antitissue antibodies, 1 LE cells, 3 a positive Paul-Bunnel-Davidsohn test without mononucleosis, 11 a negative skin test. Implications of the uncommon occurrence of these dissorders are discussed.

[髓性脾肿大的红细胞和免疫异常]。
对33例患者进行了红细胞缺陷筛查和细胞免疫和体液免疫的探索:31例为不可知性骨髓硬化伴骨髓化生,3例真性红细胞增多症伴继发性骨髓硬化。没有患者具有阵发性夜间血红蛋白尿的生物学异常特征(Marchiafava-Micheli)。21例中有19例红细胞膜上有抗原i,提示脾红细胞生成可产生未成熟红细胞。2例患者有单克隆性球蛋白异常血症,5例库姆斯试验阳性,6例血清类风湿性因子阳性,3例抗组织抗体,1例LE细胞,3例无单核细胞增多症的paul - bunnell - davidsohn试验阳性,11例皮肤试验阴性。本文讨论了这些疾病罕见发生的意义。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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