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伴有硬化性白质脑病的多囊性脂膜性骨发育异常的放射学骨改变。

Radiologic bone changes of polycystic lipomembranous osteodysplasia with sclerosing leukoencephalopathy.

作者信息

Mäkelä P, Järví O, Hakola P, Virtama P

出版信息

Skeletal Radiol. 1982;8(1):51-4. doi: 10.1007/BF00361370.

Abstract

More than 50 cases of polycystic lipomembranous osteodysplasia (PLO) with sclerosing leukoencephalopathy (SL) have been described in Finland, Sweden, Japan, and in the USA. Radiographic bone changes, including symmetrical cystic lesions in the small bones of the extremities and trabecular loss in the distal ends of the long tubular bones, represent primary abnormalities in the diagnosis of the disease. Neuropsychiatric symptoms, frontal syndrome, and pyramidal signs make the patients dangerous to themselves. They are often involved in traffic accidents and are prone to multiple spontaneous or almost spontaneous fractures. PLO usually starts with slight bone pain around the age of 20 years. Progress is very slow during the next ten years, but faster after the age of 40 years. The patients usually die before the age of 50 years having total dementia and epileptiform convulsions.

摘要

芬兰、瑞典、日本和美国已报道了50多例伴有硬化性白质脑病(SL)的多囊性脂膜性骨发育异常(PLO)病例。影像学上的骨骼改变,包括四肢小骨的对称性囊性病变以及长管状骨远端的骨小梁缺失,是该疾病诊断中的主要异常表现。神经精神症状、额叶综合征和锥体束征会使患者对自身构成危险。他们常遭遇交通事故,且易发生多处自发性或近乎自发性骨折。PLO通常在20岁左右开始出现轻微骨痛。在接下来的十年中进展非常缓慢,但40岁以后进展加快。患者通常在50岁之前死于全面性痴呆和癫痫样惊厥。

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