Komishke Bailey, Foulds Jessica L, McMillan Tamara, Avdimiretz Nicholas
Pediatrics, Stollery Children's Hospital, Edmonton, Alberta, Canada.
Pediatrics, University of Alberta Faculty of Medicine and Dentistry, Edmonton, Alberta, Canada.
BMJ Case Rep. 2021 Mar 4;14(3):e239434. doi: 10.1136/bcr-2020-239434.
A 17-year-old previously healthy man presented with a 4-week history of progressive bilateral leg swelling with discomfort and erythema, but no signs of arthritis or erythema nodosum. An incidental finding of a query pulmonary nodule on chest X-ray prompted chest CT for further evaluation, revealing bilateral hilar and mediastinal lymphadenopathy. The patient then underwent endobronchial ultrasound and transbronchial needle aspiration biopsies of mediastinal lymph nodes. Biopsies and bronchoalveolar lavage samples were negative for microbiology, including mycobacterial culture. Pathology demonstrated non-caseating granulomas consistent with a diagnosis of sarcoidosis. Weeks later, he developed arthralgias of the left metacarpophalangeal joints and erythema nodosum and was diagnosed with Löfgren syndrome, a phenomenon rarely described in the paediatric population. This case highlights an approach to lower extremity swelling as well as hilar lymphadenopathy in the paediatric population. In addition, it emphasises the importance of multidisciplinary teamwork for accurate and timely diagnoses.
一名17岁既往健康的男性,出现双侧腿部进行性肿胀4周,伴有不适和红斑,但无关节炎或结节性红斑体征。胸部X线偶然发现一个可疑肺结节,遂行胸部CT进一步评估,结果显示双侧肺门及纵隔淋巴结肿大。该患者随后接受了支气管内超声检查及纵隔淋巴结经支气管针吸活检。活检及支气管肺泡灌洗样本的微生物学检查(包括分枝杆菌培养)均为阴性。病理显示非干酪样肉芽肿,符合结节病诊断。数周后,他出现左手掌指关节疼痛及结节性红斑,被诊断为勒夫格伦综合征,这种现象在儿科人群中鲜有报道。该病例突出了儿科人群下肢肿胀及肺门淋巴结肿大的处理方法。此外,它强调了多学科团队合作对于准确及时诊断的重要性。