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作 者:周英[1] 杨艳平[1] 陈嵘祎[1] 李顺凡[1] 樊翌明[1]
机构地区:[1]广东医学院附属医院皮肤科,广东湛江524001
出 处:《皮肤性病诊疗学杂志》2010年第6期395-397,400,共4页Journal of Diagnosis and Therapy on Dermato-venereology
摘 要:目的:总结肥大细胞瘤的临床病理特点。方法:1例婴儿孤立性肥大细胞瘤的皮损活检标本行组织病理、姬姆萨染色和透射电镜检查。结果:皮损组织病理检查显示真皮内大量肥大细胞弥漫性浸润,姬姆萨染色显示胞质中存在紫红色异染颗粒。电镜检查显示浸润细胞主要为形态正常的肥大细胞,也有一些嗜酸粒细胞和巨噬细胞。高密度的夏科-莱登结晶游离于间质中,并与损伤的核染色质、细胞膜碎片、肥大细胞释放的颗粒相混合。结论:肥大细胞瘤多在出生时发病,确诊有赖于组织病理检查。Objective:To summarize the clinicopathologic features of mastocytoma. Methods:The biopsy specimen of an infant with solitary mastocytoma was detected by HE,Giemsa stain and transmission electron microscopy(TEM).Results:HE stain showed there were numerous of mast cells in the entire dermis,and Giemsa stain demonstrated the presence of purple-red metachromatic granules within cytoplasm.TEM exhibited that the cellular infiltrate was mainly composed of mast cells with normal appearance,but some eosinophils and macrophages were also noticed.Electron dense Charcot-Leyden crystals were free in stromal tissue,and admixed with damaged nuclear chromatin,membrane debris,and granules released from mastocytes.Conclusion:Mastocytoma mostly onset at birth,and its definite diagnosis depends on the histopathology.
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