Parvaiz Rasheed Tabinda, Jabeen Maryam, Ahsan Iqbal Sheikh, Khurram Saleem Muhammad, Faizan Ejaz Khawaja, Akbar Amna, Jadoon Sarosh Khan, Saleem Khan Mohammad
Internal Medicine, Abbas Institute of Medical Sciences (AIMS), Muzaffarabad, PAK.
Internal Medicine, Azad Jammu & Kashmir Medical College, Muzaffarabad, PAK.
Cureus. 2024 Oct 20;16(10):e71939. doi: 10.7759/cureus.71939. eCollection 2024 Oct.
Systemic lupus erythematosus (SLE) is a multi-organ autoimmune disease that can be easily missed due to its variable presentation. Acquired angioedema (AAE) is a rare first presentation of SLE. We report a case of a 23-year-old woman who presented to the emergency department with rapidly progressive swelling of the tongue and neck, followed by respiratory discomfort and a generalized non-itchy rash. A tracheostomy was performed to relieve her symptoms. Her history, examination, and relevant investigations all indicated SLE. She was treated with high-dose steroids, and pulse therapy with methylprednisolone was given for three days. Hydroxychloroquine was added, but she developed sepsis and an acute flare of SLE secondary to tracheostomy site infection. Subsequently, she was treated with broad-spectrum antibiotics, followed by a tapering dose of steroids and a maintenance dose of azathioprine. She responded to treatment, tracheostomy reversal was performed, and the patient was discharged.
系统性红斑狼疮(SLE)是一种多器官自身免疫性疾病,因其表现多样,很容易被漏诊。获得性血管性水肿(AAE)是SLE罕见的首发表现。我们报告一例23岁女性病例,该患者因舌部和颈部迅速进展性肿胀就诊于急诊科,随后出现呼吸不适和全身性非瘙痒性皮疹。行气管切开术以缓解其症状。她的病史、检查及相关检查均提示为SLE。给予大剂量类固醇治疗,并给予甲基泼尼松龙冲击治疗三天。加用羟氯喹,但她因气管切开部位感染继发脓毒症和SLE急性发作。随后,给予广谱抗生素治疗,接着逐渐减少类固醇剂量并给予硫唑嘌呤维持剂量。她对治疗有反应,进行了气管切开术回纳,患者出院。