医学
复发性多软骨炎
软骨炎
气道
声门下狭窄
外科
气管狭窄
皮肤病科
作者
Shu‐Jen Chang,Chong-Chen Lu,Yu-Mei Chung,Shinn-Shing Lee,Chung‐Tei Chou,De-Feng Huang
标识
DOI:10.1016/s1726-4901(09)70151-0
摘要
Relapsing polychondritis (RP) is a rare multisystemic disease characterized by recurrent inflammation of cartilaginous and noncartilaginous tissues. When laryngotracheal or bronchial cartilages are involved, the disease can be life-threatening and needs aggressive treatment. Upper airway complaints are rare as initial presentations of RP. Here, however, we present a case of RP, with initial manifestations of cough and dyspnea that were treated as bronchial asthma for 6 months. Subglottic stenosis was found in April 2003, during a bronchoscopic examination, and emergency tracheostomy was performed. Auricular and nasal chondritis and bilateral scleritis developed 3 months after tracheostomy. High doses of methylprednisolone and immunosuppressive agents were used, and active inflammation in the eyes and ears was controlled, but the patient's upper airway was completely collapsed. This case is reported with the hope of increasing awareness about the potential for early upper airway involvement in RP.
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