De Cata Angelo, Inglese Michele, Rubino Rosa, Molinaro Francesca, Mazzoccoli Gianluigi
Division of Internal Medicine, Department of Medical Sciences, IRCCS Scientific Institute and Regional General Hospital "Casa Sollievo della Sofferenza", San Giovanni Rotondo, FG, Italy.
Clin Exp Med. 2016 May;16(2):109-24. doi: 10.1007/s10238-015-0341-x. Epub 2015 Feb 12.
The group of diseases classified as seronegative spondyloarthritis or enthesoarthritis is characterized by typical osteoarticular and extra-articular manifestations. Diverse patterns of disease can affect different members of the same family and may show different features in the same patient, with clinical overlaps thwarting the differential diagnosis. An anatomo-pathological hallmark in enthesoarthritis is the inflammatory process in the synovio-entheseal sites. The inflammatory microenvironment of synovio-entheseal complex, named enthesitis, is characterized, after an initial inflammatory/erosive phase, by a subsequent phase of neobone apposition, which seems to progress independently from the previous erosive phase, suggesting that the physiopathogenetic mechanisms that underlay the two phases are driven by different pivots. The structural damage is characterized by excessive neobone formation, with the syndesmophyte as a typical lesion. The process underlying their formation is not fully understood, although there are many useful information to clarify the physiopathogenetic puzzle. The primum movens of the enthesitic process is the micro-trauma to which entheses are subject, especially in the lower limbs, for biomechanical reasons. The inflammatory process is facilitated by the sequential structure of the organ enthesis, constitutionally devoid of sub-enthesitic cortical bone and closely related to the underlying trabecular bone and the medullary vascular system. The reparative attempt from the vascular system, thanks to the activating action of certain loco-regional cytokines, such as TNF α, conditions the possible deposit in the enthesis of molecules derived from other organic sites and able, especially in HLA-B27+ subjects, to activate and self-renew an immune-mediated inflammatory process following the initial mechanical process.
归类为血清阴性脊柱关节炎或附着点炎的一组疾病具有典型的骨关节炎和关节外表现。不同的疾病模式可影响同一家族的不同成员,且在同一患者身上可能表现出不同特征,临床重叠使得鉴别诊断变得困难。附着点炎的一个解剖病理学特征是滑膜 - 附着点部位的炎症过程。滑膜 - 附着点复合体的炎症微环境,即附着点炎,在初始的炎症/侵蚀阶段之后,其特征是随后出现新骨附着阶段,这一阶段似乎独立于先前的侵蚀阶段进展,这表明构成这两个阶段基础的生理病理机制由不同的关键因素驱动。结构损伤的特征是新骨过度形成,骨桥为典型病变。尽管有许多有用信息来阐明生理病理难题,但它们形成的潜在过程尚未完全了解。附着点炎过程的首要动因是附着点所遭受的微创伤,特别是在下肢,这是由生物力学原因导致的。器官附着点的连续结构促进了炎症过程,该结构本质上缺乏附着点下皮质骨,且与下方的小梁骨和髓腔血管系统密切相关。由于某些局部细胞因子(如TNFα)的激活作用,来自血管系统的修复尝试决定了源自其他有机部位的分子在附着点沉积的可能性,并且尤其在HLA - B27阳性个体中,能够在初始机械过程之后激活并自我更新免疫介导的炎症过程。