Bone Scintigraphy in Engelmann-Camurati Disease

被引:5
|
作者
De Bonilla Damia, Alvaro [1 ]
Calvo Moron, Cinta [1 ]
De la Riva Perez, Pablo Antonio [1 ]
Cambil Molina, Teresa [1 ]
Molina Mora, Manuela [1 ]
Fernandez Fatou, Auxiliadora [1 ]
Castro Montano, Juan [1 ]
机构
[1] Hosp Univ Virgen Macarena, Dept Nucl Med, Seville, Spain
关键词
Engelmann-Camurati disease; progressive diaphyseal dysplasia; TGF beta 1 gene; bone scintigraphy; hyperostosis; PROGRESSIVE DIAPHYSEAL DYSPLASIA; MUTATION; PATIENT;
D O I
10.1097/RLU.0b013e3181e05ea3
中图分类号
R8 [特种医学]; R445 [影像诊断学];
学科分类号
1002 ; 100207 ; 1009 ;
摘要
Engelmann-Camurati Disease is a rare bone disorder with low incidence (1:1 million births). In this article, we describe the case of a patient who presented with pain in the upper and lower limbs. She had an important anxiety-depressive component in relation to pain and limitation of physical activity, crying, and anxiety symptoms. We carried out a bone scan that showed abnormal uptake of tracer in the diaphysis of long bones. Radiographic findings included cortical symmetrical thickening in the same locations, and general biochemistry was abnormal.
引用
收藏
页码:559 / 560
页数:2
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