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Regional migratory osteoporosis: a pathogenetic hypothesis based on three cases and a review of the literature.

机译:区域性迁徙性骨质疏松症:基于三例病例的病原学假设,并复习文献。

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Regional migratory osteoporosis (RMO) is a migrating arthralgia of the weight-bearing joints of the lower limb which mainly affects middle-aged males. Its aetiology is unknown. The association of RMO with generalised osteoporosis has recently been reported. A concurrent systemic osteoporosis was also reported in some cases of transient osteoporosis of the hip (TOH), a disorder closely related to RMO. In its turn, TOH is considered a reversible stage of avascular necrosis of the hip (AVN), and the aetiopathogenesis of both of them remains strongly debated. We report three cases of RMO associated with generalised severe idiopathic osteoporosis. Three men, in the fourth and fifth decades of life, complained of at least four episodes of arthralgia in the lower limbs, with a migratory pattern, radiographic focal osteoporosis and final clinical resolution. The most striking common feature of these patients was the presence of a severe systemic osteoporosis with a prevailing trabecular involvement. We suggest that a prolonged or exaggerated activation of regional acceleratory phenomena (RAP) is the cause of transient osteoporosis. Bone tissue microdamage due to osteoporosis may be the most frequent noxious stimulus that turns RAP on, and, bone tissue microfracture is the most prevalent consequence. When this pathogenetic pathway is activated, the progression from focal osteoporosis and bone marrow oedema to avascular necrosis is associated with the amount of structural damage.
机译:区域性迁徙性骨质疏松症(RMO)是下肢负重关节的迁移性关节痛,主要影响中年男性。其病因未知。最近已经报道了RMO与广泛性骨质疏松的关系。在一些短暂性髋部骨质疏松症(TOH)的病例中,也报告了并发的全身性骨质疏松症,这是一种与RMO密切相关的疾病。反过来,TOH被认为是可逆性的髋部血管坏死(AVN)阶段,并且两者的致病性仍然存在争议。我们报告了三例RMO与广泛的严重特发性骨质疏松症相关。在人生的第四和第五十年中,三名男子抱怨下肢关节痛至少四次,伴有pattern游模式,影像学上的局灶性骨质疏松症和最终的临床症状。这些患者最明显的共同特征是存在严重的全身性骨质疏松症,小梁受累占主导。我们建议,区域加速现象(RAP)的延长或过度激活是暂时性骨质疏松的原因。骨质疏松症引起的骨组织微损伤可能是打开RAP的最常见的有害刺激,而骨组织微骨折是最普遍的后果。当该致病途径被激活时,从局灶性骨质疏松和骨髓水肿到无血管坏死的进展与结构损伤的数量有关。

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