Szczepanek Daria, Shivarajpur Ambika, Boccio Eric
Pharmacology, Memorial Healthcare System, Hollywood, USA.
Emergency Medicine, Memorial Healthcare System, Hollywood, USA.
Cureus. 2024 Nov 12;16(11):e73558. doi: 10.7759/cureus.73558. eCollection 2024 Nov.
Drug reaction with eosinophilia and systemic symptoms (DRESS syndrome) is a rare and potentially life-threatening condition. Symptoms typically manifest two to eight weeks after exposure to an offending agent, such as anticonvulsants and antibiotics. Clinical features include fever, morbilliform rash, eosinophilia, lymphadenopathy, and, in severe cases, multiorgan dysfunction, including interstitial nephritis, hepatitis, and pneumonitis. This case report discusses a 55-year-old female who developed DRESS syndrome while being treated for a urinary tract infection with trimethoprim/sulfamethoxazole (TMP/SMX). Presenting with fever, dysuria, flank pain, and a widespread non-pruritic maculopapular rash, her lab results were remarkable for eosinophilia, while the urinalysis revealed mild hematuria. Computed tomography imaging ruled out nephrolithiasis and acute pyelonephritis, leading to the diagnosis of DRESS syndrome. Management focused on discontinuing TMP/SMX and initiating systemic glucocorticoids. The patient responded well to treatment and was discharged on hospital day two with prescriptions for topical and oral steroids, famotidine, and diphenhydramine. The patient was provided with follow-up instructions and return precautions. Drug reaction with eosinophilia and systemic symptoms poses unique diagnostic challenges due to its similarity to other cutaneous reactions and the delay between drug exposure and symptom onset. Early recognition and intervention are vital for preventing severe complications. Given its potential for multiorgan dysfunction and poor patient outcomes, healthcare providers must be vigilant when evaluating patients presenting with fever and rash. Comprehensive history taking and accurate reconciliation of active and recent medications are necessary to make the diagnosis. Immediate discontinuation of the offending agent is essential, while supportive care and topical or systemic glucocorticoids remain the treatment standards.
药物超敏反应伴嗜酸性粒细胞增多和全身症状(DRESS综合征)是一种罕见且可能危及生命的疾病。症状通常在接触致病药物(如抗惊厥药和抗生素)后两到八周出现。临床特征包括发热、麻疹样皮疹、嗜酸性粒细胞增多、淋巴结病,严重时还包括多器官功能障碍,如间质性肾炎、肝炎和肺炎。本病例报告讨论了一名55岁女性,她在接受甲氧苄啶/磺胺甲恶唑(TMP/SMX)治疗尿路感染时发生了DRESS综合征。患者表现为发热、排尿困难、侧腹痛和广泛的非瘙痒性斑丘疹,实验室检查结果显示嗜酸性粒细胞增多,而尿液分析显示轻度血尿。计算机断层扫描成像排除了肾结石和急性肾盂肾炎,从而诊断为DRESS综合征。治疗重点是停用TMP/SMX并开始使用全身性糖皮质激素。患者对治疗反应良好,在住院第二天出院,开具了外用和口服类固醇、法莫替丁和苯海拉明的处方。为患者提供了随访指导和复诊注意事项。药物超敏反应伴嗜酸性粒细胞增多和全身症状因其与其他皮肤反应相似以及药物暴露与症状发作之间存在延迟,带来了独特的诊断挑战。早期识别和干预对于预防严重并发症至关重要。鉴于其有导致多器官功能障碍和患者预后不良的可能性,医疗保健提供者在评估发热和皮疹患者时必须保持警惕。进行全面的病史采集以及准确核对正在使用和近期使用的药物对于做出诊断是必要的。立即停用致病药物至关重要,而支持性治疗以及外用或全身性糖皮质激素仍然是治疗标准。