Antúnez-Conde Raúl, Navarro Cuéllar Carlos, Ochandiano Santiago, Díez-Montiel Alberto, Montes Pablo, Monteserín Eduardo, Agea Marc, Gascón Dafne, Navarro Ignacio, Arenas Gema, Tousidonis Manuel, Salmerón José Ignacio
Oral and Maxillofacial Surgery Department, Hospital General Universitario Gregorio Marañón, C/Dr. Esquerdo, 46, 28007 Madrid, Spain.
Life (Basel). 2021 Oct 20;11(11):1116. doi: 10.3390/life11111116.
The appearance of cervical adenopathies can occur in many pathologies in a non-specific manner; Erdheim-Chester disease (ECD) is characterized by xanthogranulomatous and xanthomatous infiltration of different tissues with numerous foamy histiocytes. Bone lesions are frequent and radiological features are pathognomonic for diagnosis, but lymph node involvement is exceptional and is not a form of presentation reported in the literature. Recurrent BRAFV600E mutation and others have been discovered in recent years. Since then, several treatments targeting the BRAF and MEK pathways have been developed with high success rates; even so, interferon-α continues to be one of the most widely used treatments. The best imaging test for the study and monitoring of the disease is PET-CT. The prognosis of ECD is relatively poor, with a survival of 43% of patients after 32 months follow-up. Higher survival rates have been reported in patients treated with interferon. The authors present an exceptional case of ECD with cervical adenopathies as a debut, highlighting the need for the knowledge of the disease for differential diagnosis, early treatment, and the importance of communication between the clinician and the pathologist. The main features of the disease and a brief discussion of current diagnosis and treatment are reviewed.
颈部淋巴结病可非特异性地出现在多种病理状况中; Erdheim-Chester病(ECD)的特征是不同组织出现黄色瘤性和黄色瘤样浸润,伴有大量泡沫状组织细胞。骨病变常见,放射学特征对诊断具有特异性,但淋巴结受累罕见,且并非文献报道的一种表现形式。近年来已发现复发性BRAFV600E突变及其他突变。自那时起,已开发出几种针对BRAF和MEK通路的治疗方法,成功率很高;即便如此,干扰素-α仍然是最广泛使用的治疗方法之一。用于该疾病研究和监测的最佳影像学检查是PET-CT。ECD的预后相对较差,随访32个月后患者生存率为43%。接受干扰素治疗的患者报告有较高的生存率。作者介绍了一例以颈部淋巴结病为首发表现的罕见ECD病例,强调了了解该疾病以进行鉴别诊断、早期治疗的必要性,以及临床医生与病理学家之间沟通的重要性。文中回顾了该疾病的主要特征以及对当前诊断和治疗的简要讨论。