摘要
目的:探讨地中海贫血性骨病变的CT、MRI表现及诊断要点,提高该病的诊断水平。方法:回顾性分析17例地中海贫血性骨病变的CT、MRI资料,结合文献,探讨其影像特点及鉴别诊断。结果:17例胸腰椎椎体及附件均受累,其中4例合并颅骨病变,2例合并股骨及胫腓骨病变,5例合并肋骨、胸骨及肩胛骨病变。MRI见骨髓弥漫性信号异常,T_1WI骨髓高信号弥漫性降低,T_2WI呈等信号,STIR T_2WI呈高信号。CT示胸腰椎椎体呈栅栏状改变,骨小梁减少、增粗;其中5例肋骨、胸骨及肩胛骨膨胀改变,4例颅骨板障增厚、板障间呈放射状排列骨小梁;合并椎旁软组织肿块11例,合并肋骨旁软组织肿块4例,增强扫描肿块轻度均匀强化,穿刺活检示髓外造血组织。结论:地中海贫血性骨病变影像学表现有一定的特征,结合病史,可作出正确诊断。
Objective:To explore CT,MRI imaging findings and the diagnostic points of Mediterranean anemia bone lesions,so as to improve the diagnostic level of this disease. Methods:Retrospectively analyze 17 cases CT, MRI images of thalassemia os- teodystrophy combined with literature,to investigate the imaging features and differential diagnosis. Results: 17 cases of thoracic and lumbar vertebral body and accessories were involved,including 4 cases with skull lesions,2 cases with femoral,tibia and fibula lesions. MRI showed bone marrow diffuse abnormal signal,the signal on T1WI and T2WI were isointensity,and stir T2WI showed high signal;CT findings of thoracic and lumbar vertebral palisading change,bone trabeculae reduce,thickening;5 cases showed fibs,sternum and scapula expansion change,4 cases had skull diploic thickening and radial arrangement of the trabeculae in diploe;combined with paravertebral soft tissue mass in ll cases,combined rib adjacent soft tissue mass in 4 cases,the mass mild homogeneous enhanced in enhancement scanning and biopsy showed extramedullary hematopoietic tissue. Conclusion: Thalassemia osteodystrophy imaging has certain characteristics,combining with the history,we can make the correct diagnosis.
出处
《中国中西医结合影像学杂志》
2017年第3期288-290,共3页
Chinese Imaging Journal of Integrated Traditional and Western Medicine