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婴儿皮质增生症(卡菲病):骨小梁周围细胞的超微结构和免疫组织化学特征

Infantile cortical hyperostosis (Caffey disease): ultrastructural and immunohistochemical characterization of the peritrabecular cells.

作者信息

Quacci D, Pazzaglia U E, Dell'Orbo C, Ennas M G

机构信息

Dipartimento di CitoMorfologia, Universitá degli Studi, Cagliari, Italy.

出版信息

Histol Histopathol. 1990 Apr;5(2):187-92.

PMID:1724929
Abstract

The ultrastructure and the immunohistochemical pattern of the cells which are responsible for the bone resorption in the cortical infantile hyperostosis were investigated. The osteoclasts present a great positivity to MB1 antigen and a low positivity to OKM5. Mononuclear cells with primary lysosomes, looking like osteoclast ones are present in high concentration in peritrabecular spaces. These cells show a high positivity to OKM5 antigen and a low positivity to MB1 antigen. The mononuclear granulated cells are positive to tartrate-resistent acid phosphatase. The possible common origin and their co-operation in bone resorption is discussed.

摘要

对婴儿皮质性骨肥厚中负责骨吸收的细胞的超微结构和免疫组织化学模式进行了研究。破骨细胞对MB1抗原呈强阳性,对OKM5呈弱阳性。在骨小梁周围间隙中高浓度存在带有初级溶酶体、看似破骨细胞的单核细胞。这些细胞对OKM5抗原呈强阳性,对MB1抗原呈弱阳性。单核颗粒细胞对抗酒石酸酸性磷酸酶呈阳性。讨论了它们在骨吸收中可能的共同起源及其合作关系。

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