Choi Y H, Im J G, Han B K, Kim J H, Lee K Y, Myoung N H
Departments of Radiology, Dankook University College of Medicine, Choongnam, Korea.
Chest. 2000 Jan;117(1):117-24. doi: 10.1378/chest.117.1.117.
To describe the radiologic and clinical findings of Churg-Strauss syndrome (CSS) and its thoracic manifestations.
We used retrospective analysis to review and characterize the radiographic, thin-section CT, and clinical findings of CSS.
The study involved nine patients with CSS. The patients included four men and five women, whose ages ranged from 18 to 60 years (median, 35 years). Thin-section CT scans and chest radiographs were retrospectively analyzed by three radiologists in consensus. Clinical data were obtained by chart review. Histologic samples were available in eight patients.
All patients had a history of asthma averaging 28 months (range, 4 to 72 months) prior to the initial symptom of vasculitis and marked peripheral blood eosinophilia (mean peak count, 8,726/microL; range, 3,000 to 32,000/microL; mean differential count, 41%; range, 19 to 67%). All patients had systemic vasculitis involving the lung and two to four extrapulmonary organs, most commonly the nervous system (n = 8) and skin (n = 7). Chest radiographs showed bilateral nonsegmental consolidation (n = 5), reticulonodular opacities (n = 3), bronchial wall thickening (n = 3), and multiple nodules (n = 1). The most common thin-section CT findings included bilateral ground-glass opacity (n = 9); airspace consolidation (n = 5), predominantly subpleural and surrounded by the ground-glass opacity; centrilobular nodules mostly within the ground-glass opacity (n = 8); bronchial wall thickening (n = 7); and increased vessel caliber (n = 5). Other findings were hyperinflation (n = 4), larger nodules (n = 4), interlobular septal thickening (n = 2), hilar or mediastinal lymph node enlargement (n = 4), pleural effusion (n = 2), and pericardial effusion (n = 2).
In CSS, thoracic organs are invariably involved with additional diverse manifestations. The possibility of CSS should be raised in patients with a history of asthma and hypereosinophilia who present with thin-section CT findings of bilateral subpleural consolidation with lobular distribution, centrilobular nodules (especially within the ground-glass opacity) or multiple nodules, especially in association with bronchial wall thickening.
描述变应性肉芽肿性血管炎(CSS)的影像学和临床特征及其胸部表现。
我们采用回顾性分析来评估和描述CSS的X线、薄层CT及临床特征。
本研究纳入9例CSS患者。患者包括4名男性和5名女性,年龄范围为18至60岁(中位数为35岁)。由3名放射科医生共同对薄层CT扫描和胸部X线片进行回顾性分析。通过查阅病历获取临床资料。8例患者有组织学样本。
所有患者在出现血管炎初始症状前均有哮喘病史,平均病程28个月(范围为4至72个月),外周血嗜酸性粒细胞显著增多(平均峰值计数为8,726/μL;范围为3,000至32,000/μL;平均分类计数为41%;范围为19%至67%)。所有患者均有累及肺部及两至四个肺外器官的系统性血管炎,最常见的是神经系统(n = 8)和皮肤(n = 7)。胸部X线片显示双侧非节段性实变(n = 5)、网状结节状阴影(n = 3)、支气管壁增厚(n = 3)及多发结节(n = 1)。最常见的薄层CT表现包括双侧磨玻璃样密度影(n = 9);气腔实变(n = 5),主要位于胸膜下并被磨玻璃样密度影包绕;小叶中心结节大多位于磨玻璃样密度影内(n = 8);支气管壁增厚(n = 7);以及血管管径增粗(n = 5)。其他表现包括肺过度充气(n = 4)、较大结节(n = 4)、小叶间隔增厚(n = 2)、肺门或纵隔淋巴结肿大(n = 4)、胸腔积液(n = 2)及心包积液(n = 2)。
在CSS中,胸部器官总是会受累并伴有其他多种表现。对于有哮喘病史且嗜酸性粒细胞增多的患者,若薄层CT表现为双侧胸膜下小叶分布的实变、小叶中心结节(尤其是位于磨玻璃样密度影内)或多发结节,特别是伴有支气管壁增厚时,应考虑CSS的可能。