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肺泡蛋白沉着症的组织化学。对其形态发生机制的一项贡献(作者译)

[Histochemistry of the pulmonary alveolar proteinosis. A contribution to the formal pathogenesis (author's transl)].

作者信息

Kietz D, Möbius G, Eckert H

出版信息

Zentralbl Allg Pathol. 1976;120(1):45-50.

PMID:132072
Abstract

By means of histochemical methods the authors investigated 3 cases of the diffuse and 2 cases of the focal form of pulmonary alveolar proteinosis (2 women and 3 men, aged from 25 to 58 years). In the main the results of other investigators concerning distribution and occurrence of proteins and lipids are confirmed. In contrast to the results of other investigators, the authors detected acid mucopolysaccharides also in the granules of the intraal veolar substance. Presumable the injuring substance causes proliferation, desquamation, and breakdown of the alveolar cells. In this way both the granules and clots are formed, the latter ones are decomposed in steps of granules. Obviously parts of the blood are mixed with the granular part of the intraalveolar substance.

摘要

作者通过组织化学方法对3例弥漫型和2例局灶型肺泡蛋白沉积症患者(2名女性和3名男性,年龄在25至58岁之间)进行了研究。总体而言,其他研究者关于蛋白质和脂质分布及存在情况的结果得到了证实。与其他研究者的结果不同,作者还在肺泡内物质的颗粒中检测到了酸性粘多糖。推测损伤物质会导致肺泡细胞增殖、脱屑和分解。通过这种方式形成了颗粒和凝块,后者会逐步分解为颗粒。显然,部分血液与肺泡内物质的颗粒部分混合在一起。

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