嗜酸性粒细胞在坏死中的作用主要发生在单系统朗格汉斯细胞组织细胞增多症

Y. Kawabata, N. Tomichi, M. Tanino, T. Ogura, M. Kawamoto, Y. Fukushima, K. Kurashima, Y. Shimizu
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摘要

背景:单系统朗格汉斯细胞组织细胞增多症(LCH)表现为大量嗜酸性粒细胞浸润,偶尔出现坏死和囊肿/腔形成,但坏死的原因尚不清楚。嗜酸性粒细胞在单系统LCH坏死中的作用尚未被研究,因此,我们从病理学角度研究了它们的作用。方法:49例(病变50例,男30例,女19例;1998年初至2011年底22家机构的LCH患者均符合LCH病理标准。器官来源为33个肺和17个其他器官。47例为单系统LCH, 2例为不累及“危险器官”的多系统LCH。探讨了嗜酸性粒细胞与坏死、各种组织破坏的相互关系及随后的结果。我们还详细检查了早期LCH病变的细胞特征。采用常规组织病理学和免疫组织化学检查,包括抗嗜酸性粒细胞抗体。结果:30例肺LCH的破坏特征及后续表现如下:血管破坏6例;囊肿/腔形成,22;组织缺损填充,15;弹性组织,30;网状纤维破坏,17。2例死亡嗜酸性粒细胞无纤维化伴微小坏死。在细胞期病变中观察到大量朗格汉斯细胞和嗜酸性粒细胞,两者相互关联。17例非肺性LCH的破坏特征及后续表现为:不同程度的凝固性坏死,无纤维化,8例;空腔形成和细胞脱落,5;和网状光纤网络的破坏,15。在大多数坏死病灶中可见大量死亡的嗜酸性粒细胞伴脱颗粒,并可见少量沙克-莱顿晶体。坏死灶中中性粒细胞的脱粒仅限于活细胞。结论:这些发现提示LCH坏死前嗜酸性粒细胞的脱颗粒与坏死后各种组织破坏之间存在密切关系。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
The role of eosinophils in necrosis mainly in single-system Langerhans cell histiocytosis
Background: Single-system Langerhans cell histiocytosis (LCH) shows massive infiltration of eosinophils and occasional necrosis and cyst/cavity formation, but the cause of the necrosis remains unclear.The role of eosinophils in necrosis in single-system LCH has not been examined yet, and therefore,we investigated their role pathologically. Methods: Biopsy/lobectomy specimens were collected in 49 cases (50 lesions, 30 males, 19 females; mean age 31 years) satisfying the pathological criteria of LCH from 22 institutions from the beginning of 1998 to the end of 2011. Sources of organs were 33 lungs and 17 other organs. Forty-seven cases showed single-system LCH and 2 cases showed multiple-system LCH without involvement of “Risk Organs”. The interrelationship between eosinophils and necrosis, various kinds of tissue destruction, and subsequent findings were investigated. Cellular features of the earliest LCH lesion were also examined in detail. Ordinal histopathological and immunohistochemical examinations that included anti-eosinophilic antibodies were used. Results: Destructive features and subsequent findings of pulmonary LCH from 30 cases were as follows: vascular destruction, 6; cyst/cavity formations, 22; filling of tissue defect, 15;and elastic tissue, 30,and reticuline fiber destruction, 17. Tiny necroses accompanying degranulation of dead eosinophils without fibrosis werepresent in 2 cases. Large numbers of Langerhans cells and eosinophils were observed in the cellular-stage lesions and were associated with each other. Destructive features and subsequent findings of non-pulmonary LCH from 17 cases were as follows: coagulative necrosis of various extent without fibrosis, 8; cavity formation and cell shedding, 5; and reticuline fiber network destruction, 15. Large numbers of dead eosinophils accompanying degranulation were noted in most of the necrotic lesions along with a few Charcot-Leyden crystals. Degranulation of neutrophils in the necrotic lesions was limited to live cells. Conclusions: These findings suggest an intimate relationship between preceding degranulation of eosinophils in necrosis and various kinds of tissue destruction following necrosis in LCH.
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