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Automatic detection and quantification of pulmonary arterio-venous malformations in hereditary hemorrhagic telangiectasia

机译:遗传性出血性毛细血管扩张症中肺动静脉畸形的自动检测和定量

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Hereditary hemorrhagic telangiectasia (HHT) is an autosomic dominant disorder, which is characterized by the development of multiple arterio-venous malformations in the skin, mucous membranes, and/or visceral organs. Pulmonary Arterio-Venous Malformation (PAVM) is an abnormal connection where feeding arteries shunt directly into draining veins with no intervening capillary bed. This condition may lead to paradoxical embolism and hemorrhagic complications. PAVMs patients should systematically be screened as the spontaneous complication rate is high, reaching almost 50%. Chest enhanced contrast CT scanner is the reference screening and follow-up examination. When performed by experienced operators as the prime treatment, percutaneous embolization of PAVMs is a safe, efficient and sustained therapy. The accuracy of PAVM detection and quantification of its progression over time is the key of embolotherapy success. In this paper, we propose an automatic method for PAVM detection and quantification relying on a modeling of vessel deformation, i.e. local caliber increase, based on mathematical morphology. The pulmonary field and vessels are first segmented using geodesic operators. The vessel caliber is estimated by means of a granulometric measure and the local caliber increase is detected by using a geodesic operator, the h-maxdomes. The detection sensitivity can be tuned up according to the choice of the h value which models the irregularity of the vessel caliber along its axis and the PAVM selection is performed according to a clinical criterion of >3 mm diameter of the feeding artery of the PAVM. The developed method was tested on a 20 patient dataset. A sensitivity study allowed choosing the irregularity parameter to maximize the true positive ratio reaching 85.4% in average. A specific false positive reduction procedure targeting the vessel trunks of the arterio-venous tree near mediastinum allows a precision increase from 13% to 67% with an average number of 1.15 false positives per scan.
机译:遗传性出血性毛细血管扩张症(HHT)是一种常染色体显性遗传疾病,其特征是皮肤,粘膜和/或内脏器官出现了多个动静脉畸形。肺动静脉畸形(PAVM)是一种异常连接,在这种连接中,供血动脉直接分流到引流静脉中,而没有介入的毛细血管床。这种情况可能导致自相矛盾的栓塞和出血并发症。由于自发并发症发生率高,达到近50%,应该系统地筛查PAVMs患者。胸部增强CT扫描仪是参考筛查和随访检查。当由经验丰富的操作员进行主要治疗时,PAVM的经皮栓塞术是一种安全,有效和持续的治疗方法。 PAVM检测的准确性及其随时间的进展量化是栓塞治疗成功的关键。在本文中,我们基于数学形态学,提出了一种基于血管变形的模型(即局部口径增加)的PAVM检测和定量自动方法。首先使用测地线对肺野和血管进行分段。借助于口径测量法来估计容器的口径,并通过使用测地线算子h-maxdomes来检测局部口径的增加。可以根据模拟血管口径沿其轴的不规则性的h值的选择来调整检测灵敏度,并根据PAVM进食动脉直径> 3 mm的临床标准进行PAVM选择。在20位患者的数据集上测试了开发的方法。敏感性研究允许选择不规则参数以使真实阳性率最大化,平均阳性率达到85.4%。针对纵隔附近动静脉树血管主干的特定误报减少程序可将精度从13%提高到67%,每次扫描平均误报为1.15。

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