From the *Department of Rheumatic and Immunologic Diseases, Orthopedic and Rheumatologic Institute; and †Section of Heart Failure & Cardiac Transplant Medicine, Department of Cardiovascular Medicine, Heart & Vascular Institute, Cleveland Clinic, Cleveland, OH.
J Clin Rheumatol. 2013 Oct;19(7):390-2; discussion 419. doi: 10.1097/RHU.0b013e3182a6acf0.
Churg-Strauss syndrome (CSS) is a rare small-vessel vasculitis typically associated with adult-onset asthma, peripheral and tissue hypereosinophilia, migratory pulmonary infiltrates, upper respiratory tract symptoms, and clinical evidence of systemic vasculitis. Cardiac involvement is a well-recognized complication with an estimated prevalence of 60%. Heart disease is associated with poor prognosis, accounting for almost 50% mortality in CSS. We present a case of a 48-year-old woman with CSS complicated by congestive heart failure with left ventricular ejection fraction of 25%, who was initially treated with long course of high-dose steroids without any clinical or echocardiographic improvement. She was referred to our hospital 1 year later and was initiated with cyclophosphamide 2 mg/kg per day and prednisone 60 mg/d followed by slow taper. Subsequently, the patient had remarkable improvement. Patient was then transitioned to azathioprine for 1.5 years with sustained disease remission. It may be difficult to determine myocardial disease activity status versus tissue damage in CSS with prolonged duration of heart failure symptoms. This is the first case report demonstrating that CSS cardiac disease may remain active despite 1 year of corticosteroid therapy, and significant improvement or remission can still be achieved by administering more aggressive cytotoxic immunosuppressive therapy.
变应性肉芽肿性血管炎(CSS)是一种罕见的小血管血管炎,通常与成人起病的哮喘、外周和组织嗜酸性粒细胞增多、游走性肺部浸润、上呼吸道症状和全身血管炎的临床证据相关。心脏受累是一种公认的并发症,估计患病率为 60%。心脏病与预后不良相关,CSS 患者的死亡率近 50%归因于心脏病。我们报告了一例 48 岁女性 CSS 并发充血性心力衰竭,左心室射血分数为 25%,最初接受了长时间大剂量类固醇治疗,但没有任何临床或超声心动图改善。1 年后她被转诊到我们医院,开始每天接受 2 毫克/公斤环磷酰胺和 60 毫克/天泼尼松治疗,并逐渐减量。随后,患者的病情显著改善。随后患者接受了 1.5 年的硫唑嘌呤治疗,疾病持续缓解。在心力衰竭症状持续时间较长的情况下,可能难以确定 CSS 心肌疾病活动状态与组织损伤。这是首例报告表明,尽管接受了 1 年的皮质类固醇治疗,CSS 心脏疾病仍可能保持活动状态,通过给予更积极的细胞毒性免疫抑制治疗仍可获得显著改善或缓解。