Department of Radiology, Addenbrooke's Hospital, University of Cambridge, Cambridge, UK.
Br J Radiol. 2012 Jul;85(1015):905-9. doi: 10.1259/bjr/33890893. Epub 2011 Oct 18.
Erlenmeyer flask deformity is a common radiological finding in patients with Gaucher's disease; however, no definition of this deformity exists and the reported prevalence of the deformity varies widely. To devise an easily applied definition of this deformity, we investigated a cohort of knee radiographs in which there was consensus between three experienced radiologists as to the presence or absence of Erlenmeyer flask morphology.
Using the presence or absence of Erlenmeyer flask morphology as a benchmark, we measured the diameter of the femur at the level of the physeal scar and serially at defined intervals along the metadiaphysis.
A measured ratio in excess of 0.57 between the diameter of the femoral shaft 4 cm from the physis to the diameter of the physeal baseline itself on a frontal radiograph of the knee predicted the Erlenmeyer flask deformity with 95.6% sensitivity and 100% specificity in our series of 43 independently diagnosed adults with Gaucher's disease. Application of this method to the distal femur detected the Erlenmeyer flask deformity reproducibly and was simple to carry out.
Unlike diagnostic assignments based on subjective review, our simple procedure for identifying the modelling deformity is based on robust quantitative measurement: it should facilitate comparative studies between different groups of patients, and may allow more rigorous exploration of the pathogenesis of the complex osseous manifestations of Gaucher's disease to be undertaken.
埃伦迈尔氏瓶畸形是戈谢氏病患者常见的影像学表现;然而,目前尚无关于这种畸形的定义,且已有报道的畸形发生率差异很大。为了设计一种易于应用的该畸形定义,我们研究了一组膝关节 X 线片,其中三位有经验的放射科医生对埃伦迈尔氏瓶形态的存在或不存在达成了共识。
使用埃伦迈尔氏瓶形态的存在或不存在作为基准,我们测量了骺板瘢痕水平处和骨干骺端沿特定间隔处的股骨直径。
在我们的 43 例独立诊断为戈谢氏病的成年人系列中,膝关节正位 X 线片上,骺板基线处 4cm 处的股骨骨干直径与骺板基线本身直径之比大于 0.57,可预测埃伦迈尔氏瓶畸形,其灵敏度为 95.6%,特异性为 100%。该方法应用于股骨远端可重复性地检测到埃伦迈尔氏瓶畸形,且操作简单。
与基于主观评估的诊断分类不同,我们用于识别成骨畸形的简单程序是基于可靠的定量测量:它应有助于不同患者群体之间的比较研究,并可能允许更严格地探索戈谢氏病复杂骨骼表现的发病机制。