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细小病毒B19感染的巨大早幼红细胞的新型细胞形态学。

Novel cytomorphology of the giant proerythroblasts of parvovirus B19 infection.

作者信息

Koduri P R

机构信息

Division of Hematology, Cook County Hospital, Chicago, Illinois, USA.

出版信息

Am J Hematol. 1998 Jun;58(2):95-9. doi: 10.1002/(sici)1096-8652(199806)58:2<95::aid-ajh1>3.0.co;2-v.

Abstract

The morphology of the giant proerythroblasts (GPE) in air-dried and Wright-Giemsa-stained smears of bone marrow in 16 patients with pure red cell aplasia (PRCA) caused by parvovirus B19 infection is described. B19 infection was diagnosed by the presence of the virus or viral DNA and/or IgM antibodies. Twelve patients had chronic hemolytic anemia and aplastic crisis and 4 patients had AIDS with chronic PRCA. In patients with chronic hemolytic anemia and aplastic crisis, GPE were not detectable in bone marrow biopsies that showed any degree of recovery of erythropoiesis. The GPE morphology was quite variable. The early (basophilic) GPE measured 25 to 35 microm in diameter, had a narrow rim of intensely blue and often vacuolated cytoplasm with pseudopodia, round nuclei with compact uncondensed chromatin, and an indistinct and inclusion-like purple-colored tinctorial change. The "intermediate" and "late" GPE measured 25 to 45 microm in diameter and showed cytoplasmic swelling, gradual loss of cytoplasmic basophilia, and fraying of the cytoplasm with focal rupture; the nuclei showed an increase in volume, a highly uncondensed and coarse sieve-like chromatin, and 1 to 3 prominent, pale to moderate purple inclusion-like nucleoli or inclusions. Bare nuclei similar in size and chromatin pattern to those of the GPE were present in proximity to the GPE and may have arisen from the GPE by dissolution of the cytoplasm. The glassy intranuclear inclusions with central clearing, the so-called lantern cells described in formalin-fixed tissues of patients with B19 infection, were absent in all cases. These findings suggest that direct toxic cell injury rather than apoptosis may be involved in the pathogenesis of erythroid aplasia in B19 infection.

摘要

描述了16例由细小病毒B19感染引起的纯红细胞再生障碍性贫血(PRCA)患者骨髓涂片经空气干燥和瑞氏 - 吉姆萨染色后的巨大早幼红细胞(GPE)形态。通过病毒或病毒DNA和/或IgM抗体的存在诊断B19感染。12例患者患有慢性溶血性贫血和再生障碍危象,4例患者患有艾滋病并伴有慢性PRCA。在患有慢性溶血性贫血和再生障碍危象的患者中,在显示任何程度红细胞生成恢复的骨髓活检中未检测到GPE。GPE形态变化很大。早期(嗜碱性)GPE直径为25至35微米,有窄的深蓝色边缘,细胞质常有空泡,有伪足,细胞核圆形,染色质致密未凝聚,有不清晰的、类似包涵体的紫色染色变化。“中期”和“晚期”GPE直径为25至45微米,显示细胞质肿胀,细胞质嗜碱性逐渐丧失,细胞质有磨损并伴有局灶性破裂;细胞核体积增大,染色质高度未凝聚且呈粗筛状,有1至3个突出的、淡至中度紫色的类似包涵体的核仁或包涵物。与GPE大小和染色质模式相似的裸核存在于GPE附近,可能是由于GPE细胞质溶解产生的。在所有病例中均未发现B19感染患者福尔马林固定组织中描述的具有中央清亮的玻璃样核内包涵体,即所谓的灯笼细胞。这些发现表明,直接的毒性细胞损伤而非凋亡可能参与了B19感染中红系再生障碍的发病机制。

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