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1例由柳氮磺胺吡啶诱发的药物超敏反应综合征合并间质性肺炎所致抗利尿激素分泌异常综合征。

A case of drug-induced hypersensitivity syndrome induced by salazosulfapyridine combined with SIADH caused by interstitial pneumonia.

作者信息

Morinaga Yusuke, Abe Ichiro, Minamikawa Tomohiro, Ueda Yusuke, Nii Kouhei, Sakamoto Kimiya, Inoue Ritsurou, Mitsutake Takafumi, Hanada Hayatsura, Tsugawa Jun, Kurihara Kanako, Higashi Toshio

机构信息

Department of Neurosurgery, Fukuoka University Chikushi Hospital.

Department of Endocrinology and Diabetes Mellitus, Fukuoka University Chikushi Hospital.

出版信息

Drug Discov Ther. 2019;13(4):232-238. doi: 10.5582/ddt.2019.01045.

Abstract

We present a case of a patient with drug-induced hypersensitivity syndrome (DIHS) caused by salazosulfapyridine combined with syndrome of inappropriate secretion of antidiuretic hormone (SIADH) caused by interstitial pneumonia (IP). A 67-year-old man with a past history of rheumatism (RA) presented with right hemiparalysis and aphasia as the chief complaints. A diagnosis of left embolic cerebral infarction following trial therapy for RA based on computed tomography findings was made, and external decompression was performed. Salazosulfapyridine was newly started on day 7. Dabigatran was started on day 37. On day 41, the patient developed fever. On day 42, edema and erythema appeared on his face, and erythema and rash appeared on his trunk and extremities, with gradual transition to erythroderma. The drug eruption was initially attributed to the dabigatran. Various symptoms of organ dysfunction (enteritis, myocarditis, interstitial pneumonia, hepatic disorder, stomatitis, and others) then appeared and persisted; hence, a diagnosis of DIHS associated with human herpes virus 6 and cytomegalovirus infection induced by salazosulfapyridine was suggested, and the oral administration of salazosulfapyridine was discontinued on day 53. Hyponatremia was observed in association with exacerbation of IP. Due to low serum osmotic pressure and prompt improvement of the serum sodium level by fluid restriction, the SIADH was attributed to IP. In this case, steroid pulse therapy followed by gradual decrease therapy prevented worsening of the condition.

摘要

我们报告一例患者,因柳氮磺胺吡啶引起药物性超敏反应综合征(DIHS),并伴有间质性肺炎(IP)导致的抗利尿激素分泌不当综合征(SIADH)。一名67岁有风湿性关节炎(RA)病史的男性,以右侧偏瘫和失语为主要症状就诊。根据计算机断层扫描结果,在对RA进行试验性治疗后诊断为左栓塞性脑梗死,并进行了外部减压。第7天开始新使用柳氮磺胺吡啶。第37天开始使用达比加群。第41天,患者出现发热。第42天,其面部出现水肿和红斑,躯干和四肢出现红斑和皮疹,并逐渐发展为红皮病。药疹最初归因于达比加群。随后出现并持续存在各种器官功能障碍症状(肠炎、心肌炎、间质性肺炎、肝脏疾病、口腔炎等);因此,提示诊断为柳氮磺胺吡啶诱导的与人类疱疹病毒6型和巨细胞病毒感染相关的DIHS,第53天停用柳氮磺胺吡啶口服制剂。随着IP加重出现低钠血症。由于血清渗透压降低以及通过限制液体摄入血清钠水平迅速改善,SIADH归因于IP。在本病例中,采用类固醇冲击疗法后逐渐减量治疗防止了病情恶化。

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