兰德尔塞发育机理研究

F. Grases, O. Söhnel, A. Costa-Bauza, T. Loučka
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引用次数: 0

摘要

本文研究了一名形成草酸钙二水合物(COD)结石的女性患者的腔内结石(也称为Randall's塞)的形成和发展机制。部分结石与乳突尖端相连,并与乳突内部相连,在集管内呈手指状延伸。腔内结缔组织由大小不规则(30 ~ 100 μm)的COD晶体、约5%的生物羟基磷灰石(BHAP)和有机质组成。患者尿中COD和无定形磷酸钙(ACP)中度过饱和。计算中使用了最近由Robertson改进的肾脏模型。计算得到的雷诺数表明,液体在小管中的流动为纯层流,速度分布为抛物线。在Henle上升环开始时,通过非均相成核形成COD晶体。尿中COD结晶的浓度有限,被认为与结晶尿时的结晶浓度相等。考虑了自由粒子机制和固定粒子机制。自由粒子机制假设形成单晶或晶体团块,通过大小阻挡CD。混凝土尿液过饱和时,COD结晶生长缓慢,单晶无法达到粒径,沉降速度大于液体平移流速。流体动力剪切引起分散在肾元内流动的液体中的COD固体颗粒聚集。尿液中存在的COD晶体数量不足以形成阻塞贝利尼管的分形凝聚体。同样,以波斯纳簇形式存在的分形尿磷酸盐团块也不足以阻塞贝利尼管。尿中形成的COD单晶或由COD晶体或磷酸钙团簇组成的分形团聚体不能阻塞CD的开口。未固定在CD内的固体物体总是被任何方向的CD(也向上排出的CD)的尿流冲走。我们的病人的塞的形成和发展可以用固定粒子机制来解释,假设Randall塞是由直接附着在小管壁上的晶体发展而来的。堵塞物被模拟为由源自下垫层顶部的连续的COD晶体层组成的固结物。当一个层的生长停止时,它的表面被有机物质覆盖,作为新层成核的基质。堵塞发育的时间估计为COD晶体到达管道另一侧所需的时间加上当堵塞表面被一层有机物覆盖并且磷酸盐颗粒被纳入固结时晶体生长中断的时间。根据布朗运动理论估计了到达固结表面的波斯纳团的通量。这些计算表明,在结痂核附着于管壁或乳头尖后大约4个月,患者的贝利尼管被兰德尔塞阻塞。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Mechanism of Randall’s Plugs Development
Mechanism of formation and development of intraluminal concretion, also called Randall's plug, extracted from a female patient forming calcium oxalate dihydrate (COD) calculi was examined. Some of these calculi were connected to the papillary tip, and had connections with the interior of the papilla with finger-like extensions in the collecting duct (CD). The intraluminal concretion consisted of inter-grown COD crystals of irregular size (30–100 μm), approximately 5% of biological hydroxyapatite (BHAP) and an organic matter. Urine of the patient was moderately supersaturated with respect to COD and amorphous calcium phosphate (ACP). Model of kidney, recently refined by Robertson, was used in calculations. Calculated Reynolds number indicated that the flow of liquid through tubules was purely laminar with parabolic velocity profile. COD crystals formed at the beginning of ascending loop of Henle by heterogeneous nucleation. Concentration of COD crystals in urine was limited and considered equal to concentration of crystals during crystaluria. The free particle and the fixed particle mechanisms were considered. The free particle mechanism assumes formation of a single crystal or agglomerate of crystals blocking the CD by virtue of size. The growth of COD crystals at concrete urinary supersaturation was too slow for a single crystal to attain size with settling velocity faster than the translation flow rate of liquid. Hydrodynamic shear caused aggregation of COD solid particles dispersed in a liquid flowing in the nephron. Number of COD crystals present in urine was not sufficient for formation of fractal agglomerate blocking the Bellini duct. Similarly, a fractal agglomerate of urinary phosphate present in the form of Posner's clusters was not large enough to obstruct the Bellini duct. The opening of the CD could not be obstructed by a single crystal of COD or fractal agglomerate composed of either COD crystals or calcium phosphate clusters, formed in urine by virtue of size. Solid objects not immobilised inside the CD were always washed out by urine flow from the CD of any orientation (also upward-draining CD). The formation and development of plug of our patient was explained by the fixed particle mechanism assuming that Randall's plug developes from crystal(s) attached directly to the tubule wall. The plug was modelled as concretion composed of successive layers of COD crystals originating on the top of underlying layer. When growth of a layer stopped, its surface was covered by organic matter that served as a substrate for nucleation of a new layer. The time of plug development was estimated as the time a COD crystal needed to reach the opposite side of the duct plus duration of interruptions of crystalline growth when plug surface was covered by a layer of organic matter and phosphatic particles were incorporated into concretion. The flux of Posner's clusters arriving to the concretion surface was estimated from theory of Brownian motion. These calculations suggested that obstruction of the Bellini duct of our patient by the Randall's plug occurred over a period of approximately 4 months after nucleus of concretion became attached to the duct wall or on the papillary tip.
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