Ko Seien, Komuro Jin, Katsumata Yoshinori, Shiraishi Yasuyuki, Kawakami Takashi, Yamada Yoshitake, Yuasa Shinsuke, Kohno Takashi, Kosaki Kenjiro, Fukuda Keiichi
Department of Cardiology, Keio University School of Medicine, Tokyo, Japan.
Department of Radiology, Keio University School of Medicine, Tokyo, Japan.
Pulm Circ. 2020 Nov 10;10(4):2045894020954310. doi: 10.1177/2045894020954310. eCollection 2020 Oct-Dec.
Noonan syndrome is known to have various cardiovascular defects, which include pulmonary artery stenosis. Pulmonary artery stenosis is characterized by obstruction of pulmonary artery blood flow that can cause elevated pulmonary artery pressure and ventilation-perfusion inequality, which can cause dyspnea on exertion and eventually, heart failure. Although the etiology of pulmonary artery stenosis related to congenital diseases is still unknown, balloon pulmonary angioplasty has being reported to be effective to selected patients with Alagille and Williams syndromes, but not from Noonan syndrome despite of modest prevalence of pulmonary artery stenosis. Here, we report the first Noonan syndrome patient with pulmonary artery stenosis who underwent successful balloon pulmonary angioplasty. The strategy used in balloon pulmonary angioplasty was planned with careful morphologic evaluation by computed tomographic angiography, and performed with scoring balloons in a graded approach with multiple sessions. After balloon pulmonary angioplasty, we confirmed maintained dilation of lesions and symptom alleviation, suggesting that balloon pulmonary angioplasty can be performed safely on pulmonary artery stenosis in a Noonan syndrome patient.
已知努南综合征有多种心血管缺陷,其中包括肺动脉狭窄。肺动脉狭窄的特征是肺动脉血流受阻,可导致肺动脉压力升高和通气-灌注不均,进而引起劳力性呼吸困难,并最终导致心力衰竭。尽管与先天性疾病相关的肺动脉狭窄的病因仍不清楚,但据报道,球囊肺动脉血管成形术对部分患有阿拉吉耶综合征和威廉姆斯综合征的患者有效,然而对于努南综合征患者,尽管肺动脉狭窄的患病率不低,但该方法却未见效。在此,我们报告首例接受球囊肺动脉血管成形术并获得成功治疗的患有肺动脉狭窄的努南综合征患者。球囊肺动脉血管成形术采用的策略是通过计算机断层血管造影进行仔细的形态学评估来制定的,并使用分级球囊以分次、分级的方式进行操作。球囊肺动脉血管成形术后,我们确认病变扩张得以维持且症状缓解,这表明球囊肺动脉血管成形术可安全地应用于努南综合征患者的肺动脉狭窄治疗。