Werner Oscar, Pommier Victor, Guillaumont Sophie, Vincenti Marie
Paediatric and Congenital Cardiology Department, M3C Regional Reference Centre, Clinical Investigation Centre, University Hospital, 371 Avenue du Doyen Giraud, 34295 Montpellier, France.
Paediatric Cardiology and Rehabilitation Unit, St-Pierre Institute, Palavas-Les-Flots, France.
Eur Heart J Case Rep. 2023 Oct 9;7(10):ytad495. doi: 10.1093/ehjcr/ytad495. eCollection 2023 Oct.
Kawasaki disease (KD) is a rare paediatric condition that can lead to giant coronary aneurysms. Follow-up of such complex coronary lesions remains a challenge, and their management is difficult to standardize.
Our present case concerns a 17-year-old boy who suffered a giant aneurysm of the left coronary artery, complicated by an asymptomatic stenosis. During regular follow-up, his annual cardiopulmonary exercise test revealed signs of ischaemia (ST depression and premature ventricular complexes). After several further stress tests with inconsistent results, he underwent invasive coronary angiography that revealed significant stenosis with a positive fractional flow reserve (FFR).
We discuss the challenges of diagnosing and managing coronary artery stenosis in paediatric patients with KD, particularly in cases with calcified and thrombosed lesions. A multimodal approach is crucial, including non-invasive imaging, and coronary angiography with optical coherence tomography and FFR. The evaluation of the lesion and its follow-up is an important factor in anticipating the best therapeutic choice for each patient.
川崎病(KD)是一种罕见的儿科疾病,可导致巨大冠状动脉瘤。对这类复杂冠状动脉病变的随访仍然是一项挑战,并且其管理难以标准化。
我们目前的病例是一名17岁男孩,患有左冠状动脉巨大动脉瘤,并伴有无症状狭窄。在定期随访期间,他的年度心肺运动试验显示有缺血迹象(ST段压低和室性早搏)。在进行了几次结果不一致的进一步负荷试验后,他接受了有创冠状动脉造影,结果显示有严重狭窄且血流储备分数(FFR)为阳性。
我们讨论了诊断和管理KD儿科患者冠状动脉狭窄的挑战,特别是在病变钙化和血栓形成的病例中。多模式方法至关重要,包括无创成像以及采用光学相干断层扫描和FFR的冠状动脉造影。对病变的评估及其随访是为每个患者预测最佳治疗选择的重要因素。