Tamaru Hiroto, Fujii Kenichi, Otsuji Satoru, Takiuchi Shin, Hasegawa Katsuyuki, Ishibuchi Kasumi, Ishii Rui, Yamamoto Wataru, Nakabayashi Sho, Yasuda Shingo, Kusumoto Hirofumi, Taniguchi Yusuke, Kakishita Mikio, Shimatani Yuji, Higashino Yorihiko
Department of Cardiology, Higashi Takarazuka Satoh Hospital, Takarazuka, Japan.
J Cardiol Cases. 2020 Nov 20;23(5):210-213. doi: 10.1016/j.jccase.2020.11.004. eCollection 2021 May.
The development of peri-stent contrast staining (PSS) after coronary intervention with implantation of a stent is observed in approximately 1-3% of patients treated with drug-eluting stent. Although the cumulative incidences of late in-stent restenosis and stent thrombosis are significantly higher in lesions with PSS than in those without the finding, the mechanisms for the development of PSS have not yet been fully elucidated. In this report, we describe a case of rapid development of PSS with ulcer formation caused by rupture of atherogenic neointima, which was observed by serial optical coherence tomography examinations over 6 months. Protrusion of the stent-jailed underlying necrotic core toward the lumen by the contracting force might have resulted in formation of atherogenic neointima within the stent. Subsequently, rupture of this necrotic core induced by iatrogenic neointimal injury due to balloon dilation and dissolution of the accumulated necrotic core may have resulted in PSS formation 6 months after the procedure. These findings may be helpful for consideration of etiology and therapeutic strategy for lesions with PSS. < The mechanisms of peri-stent contrast staining (PSS) formation late after drug-eluting stent (DES) implantation are diverse. Rupture of atherogenic neointima with subsequent dissolution of the stent-jailed underlying plaque debris could be one of the mechanisms of rapid PSS formation after implantation of DES. An accurate assessment of lesion morphology within the stent and patient-tailored management can reduce morbidity and mortality in patients who have undergone DES implantation.>.
在接受药物洗脱支架植入的冠状动脉介入治疗患者中,约1%-3%会出现支架周围造影剂染色(PSS)。尽管有PSS的病变中晚期支架内再狭窄和支架血栓形成的累积发生率明显高于无此表现的病变,但PSS发生的机制尚未完全阐明。在本报告中,我们描述了一例因动脉粥样硬化性新生内膜破裂导致PSS快速发展并形成溃疡的病例,该病例通过连续6个月的光学相干断层扫描检查得以观察。收缩力使支架内坏死核心向管腔突出,可能导致支架内形成动脉粥样硬化性新生内膜。随后,球囊扩张引起的医源性新生内膜损伤导致该坏死核心破裂,累积的坏死核心溶解,可能在术后6个月导致PSS形成。这些发现可能有助于考虑PSS病变的病因和治疗策略。<药物洗脱支架(DES)植入后晚期支架周围造影剂染色(PSS)形成的机制多种多样。动脉粥样硬化性新生内膜破裂,随后支架内斑块碎片溶解,可能是DES植入后快速PSS形成的机制之一。准确评估支架内病变形态并进行个体化管理,可以降低接受DES植入患者的发病率和死亡率。>