Guo Ge, Zheng Danfeng, Wang Xiaohua, Wang Xinyu
Department of Radiology, Peking University Third Hospital, Beijing, 100191, China.
Department of Pathology, Peking University Third Hospital, Beijing, 100191, China.
Radiol Case Rep. 2024 Apr 13;19(7):2590-2595. doi: 10.1016/j.radcr.2024.02.087. eCollection 2024 Jul.
Erdheim-Chester Disease (ECD) is a rare form of histiocytosis characterized by xanthomatous infiltration of affected organs. We present a case of a 62-year-old man with ECD initially presenting with constrictive pericarditis. Comprehensive imaging revealed systemic involvement, including the skeleton, orbit, pituitary, lung, kidney, and retroperitoneum, despite the absence of related symptoms. The diagnosis of ECD was eventually confirmed through histopathological evidence from a CT-guided biopsy. The patient responded well to interferon-α2b treatment, with gradual symptom amelioration and improvement in imaging and laboratory findings over a 5-month follow-up period. This case highlights the importance of considering ECD in the differential diagnosis of constrictive pericarditis and the utility of multimodal imaging for accurate diagnosis and management of this rare disease. The patient's positive response to treatment also highlights the potential for effective management of ECD, particularly with early diagnosis and intervention.
厄德里希-切斯特病(ECD)是一种罕见的组织细胞增多症,其特征为受累器官出现黄色瘤样浸润。我们报告一例62岁男性ECD患者,最初表现为缩窄性心包炎。尽管没有相关症状,但综合影像学检查显示全身受累,包括骨骼、眼眶、垂体、肺、肾和腹膜后。最终通过CT引导下活检的组织病理学证据确诊为ECD。患者对干扰素-α2b治疗反应良好,在5个月的随访期内症状逐渐改善,影像学和实验室检查结果也有所改善。该病例强调了在缩窄性心包炎的鉴别诊断中考虑ECD的重要性,以及多模态成像对准确诊断和管理这种罕见疾病的实用性。患者对治疗的积极反应也凸显了有效管理ECD的潜力,尤其是早期诊断和干预。