Department of Gastroenterology, Shandong Provincial Qianfoshan Hospital, Shandong First Medical University, Jinan, Shandong, China.
Department of Gastroenterology, The First Affiliated Hospital of Shandong First Medical University & Shandong Provincial Qianfoshan Hospital, Jinan, Shandong, China.
Medicine (Baltimore). 2023 Jan 20;102(3):e32657. doi: 10.1097/MD.0000000000032657.
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome is a severe cutaneous drug reaction characterized by fever, lymphadenopathy, hematologic abnormalities, single or multiple organ involvement, and viral reactivation.[1] The most frequently reported offending drugs are aromatic antiepileptic agents, antibiotics, and allopurinol.[2] Though a relatively rare syndrome, DRESS can lead to severe multi-organ system dysfunction, and in some cases even death. DRESS is one of the severe drug eruptions in dermatological diseases, but it is difficult to diagnose for internist. In this paper, a typical drug hypersensitivity syndrome with abnormal liver function and fever as the first manifestations was reported. The objective of this study was to improve the understanding of rare drug hypersensitivity syndrome in digestion and other fields, and to avoid missed diagnosis and misdiagnosis.
A 33-year-old Chinese female was initially diagnosed with acute hepatic insufficiency. Combined with the suspicious drug history, she developed DRESS with fever, target erythema, left lymph node enlargement, hematological abnormalities, and abnormal liver function.
Combined with the above characteristics, liver toxicity is the main manifestation, accompanied by fever, mainly moderate to high fever (above 38 °C) , sporadic rash, other organs (kidney, immune system) damage, and a marked increase in eosinophil granulocytic. Therefore the patient was diagnosed with definite case of DRESS syndrome based on clinical and laboratory findings.
Hormones (methylprednisolone 60 mg/day for 12 days and 80 mg/day for 12 days) and immunoglobulins (intravenous immunoglobulin 10 g/day for 5 days and 20 g/day for 7 days) were given.
The patient was discharged from the hospital after recovery. One month after discharge, she was re-admitted to the hospital because of elevated blood sugar and was diagnosed as diabetes.
DRESS syndrome is a rare but life-threatening hypersensitivity reaction. The mortality will be very high if it's not diagnosed and treated timely. This paper presents a successful case of methylprednisolone plus intravenous immunoglobulin therapy, which provides a stronger evidence for the future diagnosis and treatment of the disease.
药物反应伴嗜酸性粒细胞增多和全身症状(DRESS)综合征是一种严重的皮肤药物反应,其特征为发热、淋巴结病、血液学异常、单个或多个器官受累以及病毒再激活。[1]最常报告的致病药物为芳香抗癫痫药、抗生素和别嘌醇。[2]尽管 DRESS 相对少见,但可导致严重多器官系统功能障碍,在某些情况下甚至导致死亡。DRESS 是皮肤科疾病中严重的药物性皮疹之一,但内科医生难以诊断。本文报道了以肝功能异常和发热为首发表现的典型药物超敏反应综合征病例,旨在提高对消化等领域罕见药物超敏反应综合征的认识,避免漏诊和误诊。
一名 33 岁的中国女性最初被诊断为急性肝功能不全。结合可疑的药物史,她出现了以发热、靶形红斑、左侧淋巴结肿大、血液学异常和肝功能异常为特征的 DRESS。
结合上述特征,肝毒性是主要表现,伴有发热,主要为中高热(>38°C)、散在皮疹、其他器官(肾脏、免疫系统)损伤和嗜酸性粒细胞粒细胞明显增加。因此,根据临床和实验室检查结果,该患者被确诊为明确的 DRESS 综合征病例。
给予激素(甲泼尼龙 60mg/天,连用 12 天,80mg/天,连用 12 天)和免疫球蛋白(静脉注射免疫球蛋白 10g/天,连用 5 天,20g/天,连用 7 天)。
患者康复后出院。出院 1 个月后,因血糖升高再次入院,被诊断为糖尿病。
DRESS 综合征是一种罕见但危及生命的过敏反应,如果不及时诊断和治疗,死亡率将非常高。本文报道了 1 例甲泼尼龙联合静脉免疫球蛋白治疗成功的病例,为今后该疾病的诊断和治疗提供了更强的证据。