Kumar Hansraj, Kumar Alok, Kumar Subodh
Pharmacology and Therapeutics, AIIMS Deoghar, Deoghar, IND.
Pathology and Laboratory Medicine, Shahid Nirmal Mahto Medical College Hospital (SNMMCH), Dhanbad, IND.
Cureus. 2023 Aug 2;15(8):e42839. doi: 10.7759/cureus.42839. eCollection 2023 Aug.
Stevens-Johnson syndrome (SJS) is a rare condition characterized by an exaggerated immune system response to triggers such as infections or drugs. It is characterized by blistering and exfoliation of the skin and affects mucosal surfaces, including the eyes, buccal cavity, and genitals. We report a case of a 50-year-old male who developed symptoms of SJS following a recent hospital admission for acute appendicitis The patient presented with fever, erythematous patches on the palms, abdomen, groins, and oral mucosa. The onset of symptoms occurred approximately four days after discharge from the hospital, where the patient had received treatment including intravenous antibiotics (Piperacillin-Tazobactam), ranitidine, tramadol, and intravenous fluids. He was diagnosed with SJS based on clinical and histopathological findings and was treated with supportive care and corticosteroids. He recovered after one week of hospitalization. This case highlights the importance of recognizing the potential risk of developing SJS following drug administration and the need for prompt identification and management of the condition to prevent complications and improve patient outcomes.
史蒂文斯-约翰逊综合征(SJS)是一种罕见疾病,其特征为免疫系统对感染或药物等触发因素产生过度反应。其特点是皮肤出现水疱和剥脱,并累及黏膜表面,包括眼睛、口腔和生殖器。我们报告一例50岁男性病例,该患者近期因急性阑尾炎住院后出现了SJS症状。患者表现为发热,手掌、腹部、腹股沟和口腔黏膜出现红斑。症状在出院后约四天开始出现,患者在住院期间接受了包括静脉注射抗生素(哌拉西林-他唑巴坦)、雷尼替丁、曲马多和静脉输液在内的治疗。根据临床和组织病理学检查结果,他被诊断为SJS,并接受了支持治疗和皮质类固醇治疗。住院一周后他康复了。该病例强调了认识到药物给药后发生SJS潜在风险的重要性,以及及时识别和处理该病症以预防并发症和改善患者预后的必要性。