Histopathological findings of late-phase restenosis after directional coronary atherectomy with drug-coated balloon angioplasty: a case report

被引:3
作者
Yamamoto, Hiroyuki [1 ,2 ]
Emoto, Takuo [3 ]
Takeda, Shintaro [3 ]
Takaya, Tomofumi [1 ,2 ,4 ]
机构
[1] Hyogo Brain & Heart Ctr, Div Cardiovasc Med, 520 Saisho Kou, Himeji, Hyogo 6700981, Japan
[2] Hyogo Prefectural Harima Himeji Gen Med Ctr, Div Cardiovasc Med, Dept Internal Med, 3-264 Kamiya Cho, Himeji, Hyogo 6708560, Japan
[3] Kobe Univ, Grad Sch Med, Div Cardiovasc Med, Dept Internal Med,Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan
[4] Kobe Univ, Grad Sch Med, Div Exploratory & Adv Search Cardiol, Chuo Ku, 7-5-1 Kusunoki Cho, Kobe, Hyogo 6500017, Japan
关键词
Case report; Directional coronary atherectomy; Drug-coated balloon; Late-phase restenosis; Neovascularization;
D O I
10.1093/ehjcr/ytac259
中图分类号
R5 [内科学];
学科分类号
1002 ; 100201 ;
摘要
Background Drug-coated balloon angioplasty after directional coronary atherectomy (DCA) allows for a stentless strategy providing good short-term outcomes; however, late-phase restenosis and its mechanism remain unclear. Moreover, histopathological evaluation for late-phase restenosis post-drug-coated balloon angioplasty after DCA has never been reported. Case summary We report the first case of late-phase restenosis post-drug-coated balloon angioplasty after DCA, wherein tissue analysis using intravascular coronary imaging and histopathology suggested neovascularization in newly developed neointimal proliferation. A 52-year-old man with a history of dyslipidaemia presented with exertional angina pectoris. He underwent percutaneous coronary intervention (PCI) with drug-coated balloon angioplasty after DCA for the proximal left anterior descending artery. Although coronary angiography after nine months revealed no restenosis, he experienced recurrent chest discomfort after 25 months. Coronary angiography confirmed late-phase restenosis, and intravascular ultrasound showed progressively developed neointima above the underlying residual plaque. Optical coherence tomography suggested developing neovascularization within the neointima. Stentless PCI with drug-coated balloon angioplasty after DCA was re-performed, and collected restenotic sample. The histopathological evaluation confirmed less-cellular neointimal proliferation with rich neovascularization and concomitant diffuse vascular endothelial growth factor (VEGF) expression. Discussion Late-phase restenosis post-drug-coated balloon angioplasty after DCA comprised less-cellular neointima, suggesting inhibition of cell proliferation by drug-coated balloon efficacy. However, diffuse VEGF expression and concomitant rich neovascularization with haemorrhage and inflammation might indicate neointimal proliferation. Further large-scale investigations of the restenotic mechanism should be performed to avoid long-term target vascular failure after drug-coated balloon angioplasty post-DCA.
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