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膝关节滑膜软骨瘤病:儿童期罕见。

Synovial chondromatosis of the knee joint: a rarity during childhood.

作者信息

Kistler W

机构信息

Kinderchirurgische Klinik, Kinderspital, Luzern, Switzerland.

出版信息

Eur J Pediatr Surg. 1991 Aug;1(4):237-9. doi: 10.1055/s-2008-1042496.

Abstract

Synovial chondromatosis is a rare disease, especially in children. We report on a 12-year old girl who suffered twice a knee trauma. She then developed an arthritis of her right knee joint and finally showed all signs of synovial chondromatosis arthroscopically. Treatment consisted of removal of loose as well as stalked chondromatous bodies by means of arthroscopy. According to Milgram (1975) the evolution of the disease progresses through three stages, starting with synovial metaplasia producing chondromas which are then shed into the joint. Kay, Freemont and Davies (1989) doubt this theory.

摘要

滑膜软骨瘤病是一种罕见疾病,尤其在儿童中更为罕见。我们报告了一名12岁女童,她曾两次遭受膝关节创伤。随后她出现了右膝关节关节炎,最终经关节镜检查显示出滑膜软骨瘤病的所有体征。治疗方法是通过关节镜切除游离的以及带蒂的软骨瘤体。根据米尔格拉姆(1975年)的研究,该病的发展过程分为三个阶段,始于滑膜化生产生软骨瘤,然后软骨瘤脱落进入关节。凯、弗里蒙特和戴维斯(1989年)对此理论表示怀疑。

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