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

机译:遗传性出血性毛细管扩诊肺动脉静脉畸形的自动检测及定量

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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Telangiectasia(HHT)是一种常染色体显性障碍,其特征在于在皮肤,粘膜和/或内脏器官中发育多个动脉静脉畸形。肺动脉静脉畸形(PAVM)是一种异常连接,在没有干预毛细床的排放静脉中,喂食动脉分流。这种情况可能导致矛盾的栓塞和出血并发症。由于自发的并发症率高,帕米斯患者应系统地筛选,达到近50%。胸部增强对比度CT扫描仪是参考筛选和后续检查。当经验丰富的运营商作为主要处理执行时,Pavms的经皮栓塞是一种安全,有效和持续的治疗。 Pavm检测和随时间的进展量化的准确性是栓塞治疗成功的关键。在本文中,我们提出了一种自动方法,用于依赖于血管变形的建模,即局部口径增加,依赖于船舶变形的建模。首先使用测地算子分段肺场和血管。通过粒度测量估计血管口径,并且通过使用测地算子,H-MaxDES来检测局部口径增加。可以根据选择H值的选择来调谐检测灵敏度,该H值沿其轴线模拟血管口径的不规则性,并且根据孔径的进给动脉的临床标准来执行PAVM选择。在20个患者数据集上测试开发的方法。允许的敏感性研究选择不规则参数,以最大化达到85.4%的真正正值。靶向亚宫内动脉树的血管树干的特异性假阳性还原过程允许精度从13%增加到67%,平均每次扫描的1.15误阳性。

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