Ru Yong-Xin, Zhu Xiao-Fan, Gao Jing-Tao, Wang Hui-Jun, Zhao Shi-Xuan, Feng Min, Liu Jin-Hua, Liu En-Bing, Chen Yu-Mei, Zhen Yi-Zhou
Institute of Hematology & Blood Diseases Hospital, Chinese Academy of Medical Sciences and Peking Union Medical College, Tianjin, China.
Ultrastruct Pathol. 2008 May-Jun;32(3):81-8. doi: 10.1080/01913120802063099.
The objective of this study was to investigate the ultrastructural characteristics of nucleated cells in the bone marrow of patients with aplastic anemia (AA). This was done by observing the morphology of nucleated cells in bone marrow aspirates from 20 patients with AA by transmission electron microscopy. Erythroblasts were decreased in all cases and not observed in 6 cases. Nuclear abnormalities, such as pyknosis, karyolysis, karyorrhexis, apoptosis, and "Swiss cheese"-like changes, were found in 10 cases. Focal cytoplasmic necrotic changes and cytolysis were found in 3 cases. There were more megaloblasts in 4 cases. Abnormalities of granulocytes were found in 12 out of 18 cases. Megakaryocytes showed focal cytoplasmic necrotic changes. Most monocytes had dendritic features, including excessive cytoplasm, processes, and large round nuclei in all cases. Other monocytes illustrated typical monocytic features with twisted nuclei, plentiful RER, vacuoles, lysosomes, and prominent Golgi apparatus. Macrophages and hemophagocytes occurred in all cases. The incidence of lymphocytes was high in 17 out of 20 cases and occasionally lymphocytes were enlarged in 8 cases. More plasmacytes and plasmacytoid lymphocytes were found in 5 and 3 cases, respectively. The observations suggest that (1) the universal nuclear injury of erythroblasts may be related to the pathogenetic pathway of AA development; (2) the dendritic cells and hemophagocytes from the mononuclear phagocyte system may play a more critical role in hematopoietic failure of AA, directly and/or indirectly; and (3) besides T lymphocytes, increasing numbers of plasmacytes or plasmacytoid lymphocytes are associated with AA in some cases.
本研究的目的是探讨再生障碍性贫血(AA)患者骨髓中有核细胞的超微结构特征。通过透射电子显微镜观察20例AA患者骨髓穿刺物中有核细胞的形态来完成此项研究。所有病例中幼红细胞均减少,6例未观察到幼红细胞。10例发现核异常,如核固缩、核溶解、核碎裂、凋亡和“瑞士奶酪”样改变。3例发现局灶性细胞质坏死改变和细胞溶解。4例中有较多巨幼红细胞。18例中有12例发现粒细胞异常。巨核细胞表现出局灶性细胞质坏死改变。所有病例中大多数单核细胞具有树突状特征,包括细胞质过多、突起和大的圆形核。其他单核细胞表现出典型的单核细胞特征,核扭曲,粗面内质网丰富,有液泡、溶酶体和明显的高尔基体。所有病例中均有巨噬细胞和噬血细胞。20例中有17例淋巴细胞发生率高,8例偶尔有淋巴细胞增大。分别在5例和3例中发现更多的浆细胞和浆细胞样淋巴细胞。这些观察结果表明:(1)幼红细胞普遍的核损伤可能与AA发生发展的致病途径有关;(2)来自单核吞噬细胞系统的树突状细胞和噬血细胞可能在AA的造血衰竭中直接和/或间接发挥更关键的作用;(3)除T淋巴细胞外,在某些情况下,越来越多的浆细胞或浆细胞样淋巴细胞与AA有关。