Unusual Cortical Bone Features in a Patient with Gorlin-Goltz Syndrome: A Case Report

被引:2
|
作者
Tarnoki, Adam Domonkos [1 ]
Tarnoki, David Laszlo [1 ]
Kiss, Katalin Klara [1 ]
Bata, Pal [1 ]
Karlinger, Kinga [1 ]
Banvolgyi, Andras [2 ]
Wikonkal, Norbert [2 ]
Berczi, Viktor [1 ]
机构
[1] Semmelweis Univ, Dept Radiol & Oncotherapy, H-1085 Budapest, Hungary
[2] Semmelweis Univ, Dept Dermatol Venerol & Skin Oncol, H-1085 Budapest, Hungary
关键词
Basal Cell Nevus Syndrome; Lower Extremity; Tomography; X-Ray Computed; RISK;
D O I
10.5812/iranjradiol.5316
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
Gorlin-Goltz syndrome (GGS) consists of ectodermal and mesodermal abnormalities. In this case report we will investigate lower extremity lesions of GGS. A 52-year-old man with GGS underwent skull and lower extremity computer tomography. Radiographic findings included cervical spondylosis, transparent areas with slurred margins, and cerebral falx calcification. Tibial and fibular specific cortical lesions (thin cortical and subcortical cystic lesions) were seen on the radiography, which was confirmed by computer tomography. To our knowledge, this is the first report of such a long lesion of the tibia and fibula. Specific lower extremity cortical lesions (thin cortical and subcortical cystic lesions) may occur and these abnormalities can be found on radiography or CT, which are most probably attributed to retinoid treatment.
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页数:4
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