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系统性肥大细胞增多症中肥大细胞的超微结构特征。

Ultrastructural features of mast cells in systemic mastocytosis.

作者信息

Naveh Y, Ludatscher R, Gellei B, Haim S, Friedman A

出版信息

Acta Derm Venereol. 1975;55(6):443-50.

PMID:55036
Abstract

A 3-year-old boy with systemic mastocytosis has been observed since the age of 4 months when he was first diagnosed as suffering from urticaria pigmentosa. Involvement of skin, liver, spleen and bones was observed. The electron microscopy of skin and liver revealed varied alterations in the morphology of mast cells. The most important findings were irregularly-shaped cells and unusual long and interdigitated cytoplasmic villi, with consequent aggregation of mast cells which was more prominent in the dermis. Proliferation and accumulation of mitochondria in one part of the cell and deeply indented nuclei were frequent. The problem, whether the morphological changes encountered--especially the complex interdigitation of villi--should be interpreted as a sign of expected neoplastic development, is discussed.

摘要

一名3岁全身性肥大细胞增多症男孩自4个月大首次被诊断为色素性荨麻疹以来就受到观察。观察到皮肤、肝脏、脾脏和骨骼受累。皮肤和肝脏的电子显微镜检查显示肥大细胞形态有多种改变。最重要的发现是细胞形状不规则以及异常长且相互交错的细胞质绒毛,随之而来的是肥大细胞聚集,在真皮中更为明显。细胞的一部分线粒体增殖和聚集以及细胞核深陷很常见。文中讨论了所遇到的形态学变化——尤其是绒毛的复杂交错——是否应被解释为预期肿瘤发展迹象的问题。

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