Morawietz L, Classen R-A, Schröder J H, Dynybil C, Perka C, Skwara A, Neidel J, Gehrke T, Frommelt L, Hansen T, Otto M, Barden B, Aigner T, Stiehl P, Schubert T, Meyer-Scholten C, König A, Ströbel P, Rader C P, Kirschner S, Lintner F, Rüther W, Bos I, Hendrich C, Kriegsmann J, Krenn V
Institute für Pathologie, University Hospital Charité, Berlin, Germany.
J Clin Pathol. 2006 Jun;59(6):591-7. doi: 10.1136/jcp.2005.027458.
The introduction of clearly defined histopathological criteria for a standardised evaluation of the periprosthetic membrane, which can appear in cases of total joint arthroplasty revision surgery.
Based on histomorphological criteria, four types of periprosthetic membrane were defined: wear particle induced type (detection of foreign body particles; macrophages and multinucleated giant cells occupy at least 20% of the area; type I); infectious type (granulation tissue with neutrophilic granulocytes, plasma cells and few, if any, wear particles; type II); combined type (aspects of type I and type II occur simultaneously; type III); and indeterminate type (neither criteria for type I nor type II are fulfilled; type IV). The periprosthetic membranes of 370 patients (217 women, 153 men; mean age 67.6 years, mean period until revision surgery 7.4 years) were analysed according to the defined criteria.
Frequency of histopathological membrane types was: type I 54.3%, type II 19.7%, type III 5.4%, type IV 15.4%, and not assessable 5.1%. The mean period between primary arthroplasty and revision surgery was 10.1 years for type I, 3.2 years for type II, 4.5 years for type III and 5.4 years for type IV. The correlation between histopathological and microbiological diagnosis was high (89.7%), and the inter-observer reproducibility sufficient (85%).
The classification proposed enables standardised typing of periprosthetic membranes and may serve as a tool for further research on the pathogenesis of the loosening of total joint replacement. The study highlights the importance of non-infectious, non-particle induced loosening of prosthetic devices in orthopaedic surgery (membrane type IV), which was observed in 15.4% of patients.
引入明确的组织病理学标准,用于标准化评估假体周围膜,这种膜可出现在全关节置换翻修手术病例中。
基于组织形态学标准,定义了四种类型的假体周围膜:磨损颗粒诱导型(检测到异物颗粒;巨噬细胞和多核巨细胞占据至少20%的面积;I型);感染型(有中性粒细胞、浆细胞且磨损颗粒极少或无的肉芽组织;II型);混合型(I型和II型的特征同时出现;III型);以及不确定型(既不符合I型标准也不符合II型标准;IV型)。根据既定标准分析了370例患者(217名女性,153名男性;平均年龄67.6岁,翻修手术前平均时间7.4年)的假体周围膜。
组织病理学膜类型的频率为:I型54.3%,II型19.7%,III型5.4%,IV型15.4%,不可评估的为5.1%。初次关节置换与翻修手术之间的平均时间,I型为10.1年,II型为3.2年,III型为4.5年,IV型为5.4年。组织病理学诊断与微生物学诊断之间的相关性较高(89.7%),观察者间的可重复性足够(85%)。
所提出的分类方法能够对假体周围膜进行标准化分型,并可能作为进一步研究全关节置换松动发病机制的工具。该研究强调了在骨科手术中假体装置非感染性、非颗粒诱导性松动(IV型膜)的重要性,在15.4%的患者中观察到了这种情况。