Divisions of Allergy, Asthma, and Clinical Immunology Department of Internal Medicine, Gwangju, Korea.
Gastroenterology, Department of Internal Medicine, Gwangju, Korea.
Gut Liver. 2019 Mar 15;13(2):183-190. doi: 10.5009/gnl18266.
BACKGROUND/AIMS: Although eosinophilic liver infiltration (ELI) is not rare, few data exist regarding its clinical characteristics and etiology. Therefore, we evaluated these aspects to better understand the clinical implications of this lesion type, which is reasonably common in Korea.
Patients suspected of having ELI, based on abdominal computed tomography results obtained between January 2010 and September 2017, were enrolled in this retrospective study. The presumptive etiologies of ELI were categorized as parasite infections, hypereosinophilic syndrome (HES), eosinophilic granulomatosis with polyangiitis (EGPA), malignancies, and unidentified. Clinical courses and treatment responses were also evaluated.
The mean age of the enrolled patients (male, 237/328) was 62 years. Most patients (63%) were diagnosed incidentally and had peripheral eosinophilia (90%). Only 38% of the enrolled patients (n=126) underwent further evaluations to elucidate the etiology of the suspected ELI; 82 (25%) had parasite infections, 31 (9%) had HES, five (2%) had EGPA, and five (2%) had drug reactions in conjunction with eosinophilia and systemic symptoms. Almost half of the other enrolled patients had cancer. Radiologic resolution was achieved in 191 patients (61%; median time to radiologic resolution, 185 days). Resolution of peripheral eosinophilia was achieved in 220 patients (79%). In most cases, the course of ELI was benign.
This large ELI study is unique in that the incidence rate, underlying diseases, and clinical courses were comprehensively evaluated. Clinicians should investigate the etiology of ELI, as several of the underlying diseases require intervention rather than observation.
背景/目的:尽管嗜酸性粒细胞性肝浸润(ELI)并不罕见,但关于其临床特征和病因的数据很少。因此,我们评估了这些方面,以更好地了解这种病变类型的临床意义,这种病变类型在韩国相当常见。
本回顾性研究纳入了 2010 年 1 月至 2017 年 9 月期间根据腹部计算机断层扫描结果怀疑患有 ELI 的患者。将 ELI 的推测病因分为寄生虫感染、高嗜酸性粒细胞综合征(HES)、嗜酸性粒细胞肉芽肿伴多血管炎(EGPA)、恶性肿瘤和未确定原因。还评估了临床过程和治疗反应。
纳入患者的平均年龄(男性 237/328)为 62 岁。大多数患者(63%)是偶然诊断的,外周血嗜酸性粒细胞增多(90%)。只有 38%(n=126)的患者进行了进一步评估以阐明疑似 ELI 的病因;82 例(25%)有寄生虫感染,31 例(9%)有 HES,5 例(2%)有 EGPA,5 例(2%)有药物反应伴嗜酸性粒细胞增多和全身症状。其他纳入患者中有近一半患有癌症。191 例(61%;影像学缓解的中位时间为 185 天)患者的影像学缓解。220 例(79%)患者的外周血嗜酸性粒细胞增多缓解。在大多数情况下,ELI 的病程是良性的。
这项大型 ELI 研究的独特之处在于全面评估了发病率、基础疾病和临床过程。临床医生应调查 ELI 的病因,因为一些基础疾病需要干预而不是观察。