Hippel - Lindau病的多模态诊断。病例报告

IF 2.2 Q2 RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING
D. S. Stegura, R. Konovalov, M. Krotenkova, M. Dreval’, P. Anufriev, A. N. Kovaleva, D. D. Kuryshev
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引用次数: 0

摘要

希佩尔-林道病是一种罕见的遗传性联合病理,其特点是中枢神经系统、肾脏、胰腺、肾上腺发生多种良恶性肿瘤,引起广泛的临床表现。综合诊断方法使用各种成像技术,如超声、磁共振成像、计算机断层扫描和基因检测是成功治疗的一个组成部分。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Multimodal Approach in the Diagnosis of Hippel – Lindau Disease. Case Report
Hippel-Lindau  disease is a rare hereditary combined pathology characterized by development of a variety of benign and malignant tumors in the central nervous system, kidneys, pancreas, adrenal glands, which causes a wide range of clinical manifestations. A comprehensive diagnostic approach using various imaging techniques such as ultrasound, magnetic resonance imaging, computed tomography, and genetic testing is an integral part of successful treatment.
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来源期刊
Radiology Research and Practice
Radiology Research and Practice RADIOLOGY, NUCLEAR MEDICINE & MEDICAL IMAGING-
自引率
0.00%
发文量
17
审稿时长
17 weeks
期刊介绍: Radiology Research and Practice is a peer-reviewed, Open Access journal that publishes articles on all areas of medical imaging. The journal promotes evidence-based radiology practice though the publication of original research, reviews, and clinical studies for a multidisciplinary audience. Radiology Research and Practice is archived in Portico, which provides permanent archiving for electronic scholarly journals, as well as via the LOCKSS initiative. It operates a fully open access publishing model which allows open global access to its published content. This model is supported through Article Processing Charges. For more information on Article Processing charges in gen
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