Orzincolo C, Castaldi G, Scutellari P N, Vita F, Bagni B
Servizio di Radiologia e Medicina Nucleare, Arcispedale S. Anna, Ferrara.
Radiol Med. 1993 Jan-Feb;85(1-2):23-7.
The authors evaluated the prevalence of the thalassemia trait in a general population affected with femoral neck fractures. Our research was aimed at assessing whether hemoglobinopathy might affect osteoporosis, which is responsible for femoral fractures. Two hundred and thirty-eight patients admitted to St. Anna Hospital, Ferrara, for proximal femoral fractures, were retrospectively studied. The patients were 68 males and 170 females, aged 58 to 83 years (mean age: 70.4 years). The thalassemia trait was seen in 11.76% of cases, versus in 7-8% of the general population. The high prevalence of heterozygous beta-thalassemic subjects probably means that the beta-thalassemia condition is a further "variable" which is responsible for the more frequent occurrence of fractures of the proximal femur and is certainly related to an osteopenic condition much more severe than usual.
作者评估了股骨颈骨折普通人群中地中海贫血特征的患病率。我们的研究旨在评估血红蛋白病是否可能影响导致股骨骨折的骨质疏松症。对费拉拉圣安娜医院收治的238例股骨近端骨折患者进行了回顾性研究。患者包括68名男性和170名女性,年龄在58至83岁之间(平均年龄:70.4岁)。地中海贫血特征在11.76%的病例中出现,而普通人群中的比例为7%-8%。杂合子β地中海贫血患者的高患病率可能意味着β地中海贫血状况是导致股骨近端骨折更频繁发生的另一个“变量”,并且肯定与比平常严重得多的骨质减少状况有关。