单位：[1]Departments of Nuclear Medicine,Beijing Friendship Hospital of Capital Medical University, Xi Cheng District, Beijing, China.医技科室影像中心核医学科首都医科大学附属北京友谊医院[2]Departments of Radiology, Beijing Friendship Hospital of Capital Medical University, Xi Cheng District, Beijing, China.首都医科大学附属北京友谊医院
A 5-year-old boy was admitted due to shortness of breath. Blood gas analysis showed hypoxemia. However, thoracic and abdominal CT, brain MRI, and MR angiography were all normal. A Tc-MAA pulmonary scintigraphy revealed right-to-left shunting of the blood. Further genetic analysis showed the mutations in the activin receptor-like kinase 1 gene, and a diagnosis of hereditary hemorrhagic telangiectasia was made.
第一作者单位：[1]Departments of Nuclear Medicine,Beijing Friendship Hospital of Capital Medical University, Xi Cheng District, Beijing, China.
通讯作者：
通讯机构：[1]Departments of Nuclear Medicine,Beijing Friendship Hospital of Capital Medical University, Xi Cheng District, Beijing, China.[*1]Department of NuclearMedicine, Beijing Friendship Hospital of Capital Medical University, 95 Yong An Rd, Xi Cheng District, Beijing 100050, China.
推荐引用方式(GB/T 7714)：
Yang Fang,Yuan Leilei,Ma Daqing,et al.Tc-99m-MAA Pulmonary Scintigraphy in Hereditary Hemorrhagic Telangiectasia[J].CLINICAL NUCLEAR MEDICINE.2016,41(8):671-673.doi:10.1097/RLU.0000000000001249.
