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先天性纤维蛋白原异常中的骨骼变化。

Skeletal changes in congenital fibrinogen abnormalities.

作者信息

Lagier R, Bouvier C A, Van Strijthem N

出版信息

Skeletal Radiol. 1980;5(4):233-9. doi: 10.1007/BF00580596.

Abstract

We report an anatomico-radiologic study of humerus, femur, and tibia from a case of total congenital afibrinogenemia. Juxtatrabecular hemorrhages occur mainly in metaphyses and seem to be related to normal lines of stress. They may lead to the formation of intraosseous cysts and to a remodelling of bone trabeculae. The radiologic lesions in a second case, diagnosed as congenital dysfibrinogenemia, are similar to those found in Case 1 (femoral trabeculae remodelling) but also resemble some alterations described in hemophilia (pseudotumor of the right iliac bone). Anatomic study of the lesions in Case 2 was not possible. The significance of these observations could be better defined by a more extended skeletal study (radiologic and when feasible anatomic) of patients with congenital clotting defects and especially with inherited disorders of the fibrinogen molecule. It would also be worthwhile investigating manifest or latent hemostatic disorders (particularly at the fibrinogen level) in patients with solitary or aneurysmal bone cysts, and even with bone infarct or unexplained trabecular remodelling.

摘要

我们报告了一例完全先天性无纤维蛋白原血症患者肱骨、股骨和胫骨的解剖放射学研究。小梁旁出血主要发生在干骺端,似乎与正常应力线有关。它们可能导致骨内囊肿的形成和骨小梁的重塑。第二例被诊断为先天性异常纤维蛋白原血症的放射学病变与第一例(股骨小梁重塑)相似,但也类似于血友病中描述的一些改变(右髂骨假肿瘤)。对第二例病变进行解剖学研究是不可能的。通过对先天性凝血缺陷患者,尤其是纤维蛋白原分子遗传性疾病患者进行更广泛的骨骼研究(放射学研究以及可行时的解剖学研究),可以更好地明确这些观察结果的意义。对孤立性或动脉瘤性骨囊肿患者,甚至是骨梗死或不明原因小梁重塑患者,研究明显或潜在的止血障碍(特别是在纤维蛋白原水平)也将是值得的。

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