Assistance Publique des Hôpitaux de Marseille (APHM), Hôpital Nord, Service de Médecine Interne, Aix-Marseille Université (AMU), Marseille, France.
Assistance Publique des Hôpitaux de Marseille (APHM), Hôpital de la Timone, Service de Médecine Interne, Gériatrie et Thérapeutique, Aix-Marseille Université (AMU), Marseille, France.
Rheumatol Int. 2022 Nov;42(11):2013-2018. doi: 10.1007/s00296-022-05137-w. Epub 2022 May 7.
Giant cell arteritis (GCA) is the most frequent vasculitis affecting adults aged > 50 years. Cardiac involvement in GCA is considered rare, and only a few cases of pericarditis have been reported. The aim of this study was to determine the characteristics and prognosis of GCA patients suffering from pericardial involvement at diagnosis.
We conducted a single-centre, retrospective chart review of patients with GCA in internal medicine departments (from 2000 to 2020). Patients were identified through a centralized hospital database. We retrospectively collected demographic, clinicobiological, histological, imaging, treatment and outcome data. Patients with pericardial effusion, defined as an effusion visible on the CT-scan performed at GCA diagnosis were compared to those without pericardial involvement.
Among the 250 patients with GCA, 23 patients (9.2%) had pericardial effusion on CT-scan. The comparison between the groups revealed similar distribution of age, gender, cranial symptoms and ocular ischaemic complications. Patients with pericardial effusion had a higher frequency of weight loss. They also had lower haemoglobin levels and higher platelet levels (p = 0.006 and p = 0.002, respectively), and they more frequently had positive temporal artery biopsy. There were no differences concerning the treatment, relapses, follow-up duration or deaths.
This case series sheds light on GCA as a cause of unexplained pericardial effusion or symptomatic pericarditis among adults aged > 50 years and elevated inflammatory biological markers. Fortunately, pericardial involvement is a benign GCA manifestation. In that context, the search for constitutional symptoms, cranial symptoms and associated signs of polymyalgia rheumatica is crucial for rapidly guiding GCA diagnosis.
巨细胞动脉炎(GCA)是最常见的影响 50 岁以上成年人的血管炎。GCA 中心脏受累被认为很少见,仅有少数心包炎病例报告。本研究旨在确定诊断时患有心包受累的 GCA 患者的特征和预后。
我们对内科部门的 GCA 患者(2000 年至 2020 年)进行了单中心回顾性病历回顾。通过集中式医院数据库识别患者。我们回顾性收集人口统计学、临床生物学、组织学、影像学、治疗和结局数据。在 CT 扫描诊断 GCA 时发现有心包积液的患者与无心包受累的患者进行比较。
在 250 例 GCA 患者中,23 例(9.2%)在 CT 扫描上有心包积液。两组之间的比较显示,年龄、性别、颅部症状和眼部缺血性并发症的分布相似。有心包积液的患者体重减轻的频率更高。他们的血红蛋白水平较低,血小板水平较高(p=0.006 和 p=0.002),并且更频繁地出现阳性颞动脉活检。治疗、复发、随访时间或死亡方面没有差异。
本病例系列研究表明,GCA 是 50 岁以上成年人不明原因心包积液或有症状心包炎以及炎症生物标志物升高的原因。幸运的是,心包受累是 GCA 的良性表现。在这种情况下,寻找全身性症状、颅部症状和与风湿性多肌痛相关的体征对于快速指导 GCA 诊断至关重要。