Asymptomatic course of Forestier's disease (clinical case)

G. S. Karavaeva
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Abstract

Diffuse idiopathic skeletal hyperostosis, or Forestier's disease, is a rare disease of the musculoskeletal system, leading to calcification of ligaments and tendons and, as a consequence, to ankylosing due to bone proliferation in the places of the tendon and ligamentous apparatus of the spine. As radiation imaging shows, the disease features are uniform ossification of anterior longitudinal ligament, mainly of thoracic spine, as well as damage to entheses. The disease may be detected accidentally and not manifest itself for many years, or it may be asymptomatic. In some cases, Forestier's disease can be characterized by pain in the back, limited movement in the spine. The development theory of Forestier's disease, leading to calcification, is based on an excessive number of growth factors, such as insulin-like growth factor 1, insulin, transforming growth factor beta 1, prostaglandins I2 and endothelin 1, platelet growth factor, leading to the transformation of mesenchymal cells into fibroblasts and osteoblasts. There is an opinion that the lesion of the left longitudinal ligament occurs extremely rarely, unlike the right one, since due to the pulsation of the descending aorta there is a so-called protective effect and a mechanical barrier. A described clinical case is an accidental radiological finding.
弗赖斯节病无症状病程(附临床一例)
弥漫性特发性骨骼肥厚症,或弗赖斯季病,是一种罕见的肌肉骨骼系统疾病,导致韧带和肌腱钙化,结果,由于脊柱肌腱和韧带器官的骨增生而导致强直性。放射影像学表现为以胸椎为主的前纵韧带均匀骨化,并有椎弓根损伤。这种疾病可能是偶然发现的,多年不表现出来,也可能是无症状的。在某些情况下,弗赖斯节病的特点是背部疼痛,脊柱活动受限。导致钙化的foretier病的发展理论是基于过量的生长因子,如胰岛素样生长因子1、胰岛素、转化生长因子β 1、前列腺素I2和内皮素1、血小板生长因子,导致间充质细胞转化为成纤维细胞和成骨细胞。有一种观点认为,与右纵韧带不同,左纵韧带病变的发生极为罕见,因为降主动脉的搏动有一种所谓的保护作用和机械屏障。描述的临床病例是一个偶然的放射发现。
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