School of Clinical Medicine, Shandong Second Medical University, Weifang, China.
Department of Otorhinolaryngology, Linyi People's Hospital, Linyi, China.
Medicine (Baltimore). 2024 Oct 11;103(41):e40106. doi: 10.1097/MD.0000000000040106.
Relapsing polychondritis (RP) is a rare immune-mediated disease that leads to progressive cartilage destruction, notably affecting the ears, nose, and airways. Timely diagnosis is essential to prevent irreversible airway damage and life-threatening complications. This study presents a case of a 12-year-old child diagnosed with RP, emphasizing the critical need for timely identification of RP in children.
A 12-year-old girl was admitted with worsening hoarseness and cough, leading to respiratory distress and severe bradycardia, requiring transfer to the pediatric intensive care unit. After successful resuscitation and tracheal intubation, imaging showed significant subglottic swelling. She received antibiotics, corticosteroids, and nebulization. Despite initial stabilization, she required a tracheostomy 2 months post-discharge due to recurrent dyspnea. Six months later, she developed joint pain and a saddle nose deformity.
The patient was clinically diagnosed with RP in accordance with the diagnostic standards set forth by Micheet et al.
During the initial phase of treatment, the patient was administered antibiotics, corticosteroids, and nebulization therapy. Due to severe respiratory distress, an emergency tracheostomy was performed by ear, nose, and throat surgeons. After a definitive diagnosis, the patient was treated with tocilizumab, methotrexate, and corticosteroid therapy. Additionally, supportive measures including calcium supplementation, gastric protection, and immune support were provided.
Three years post-diagnosis, the patient's condition is stable.
Due to RP low prevalence, diagnosis in children is frequently delayed or overlooked. Notably, involvement of the major airways is more common and severe in pediatric patients compared to adults. It is crucial for Otolaryngologists to have a comprehensive understanding of this condition to effectively diagnose and manage complications associated with RP.
复发性多软骨炎(RP)是一种罕见的免疫介导性疾病,可导致进行性软骨破坏,主要影响耳朵、鼻子和气道。及时诊断对于预防气道不可逆损伤和危及生命的并发症至关重要。本研究报告了一例 12 岁儿童确诊为 RP 的病例,强调了及时识别儿童 RP 的重要性。
一名 12 岁女孩因声音嘶哑和咳嗽加重而入院,导致呼吸困难和严重心动过缓,需要转入儿科重症监护病房。在成功复苏和气管插管后,影像学显示声门下明显肿胀。她接受了抗生素、皮质类固醇和雾化吸入治疗。尽管最初病情稳定,但在出院后 2 个月因反复呼吸困难需要进行气管造口术。6 个月后,她出现关节疼痛和鞍鼻畸形。
根据 Micheet 等人制定的诊断标准,临床诊断该患者为 RP。
在治疗的初始阶段,患者接受了抗生素、皮质类固醇和雾化吸入治疗。由于严重的呼吸困难,耳鼻喉科医生紧急进行了气管切开术。明确诊断后,患者接受了托珠单抗、甲氨蝶呤和皮质类固醇治疗。此外,还提供了钙补充、胃保护和免疫支持等支持性措施。
诊断后 3 年,患者病情稳定。
由于 RP 发病率低,儿童的诊断经常被延迟或忽视。值得注意的是,与成人相比,儿童的主要气道受累更常见且更严重。耳鼻喉科医生全面了解这种疾病对于有效诊断和管理 RP 相关并发症至关重要。