Drug Reaction with Eosinophilia and Systemic Symptoms Syndrome in a Child with Cystic Fibrosis.

IF 0.7 Q4 IMMUNOLOGY Case Reports in Immunology Pub Date : 2023-01-01 DOI:10.1155/2023/1006376
Ahmed Abushahin, Haneen Toma, Sara G Hamad, Mutasim Abu-Hasan
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引用次数: 1

Abstract

Background: Drug reaction with eosinophilia and systemic symptoms (DRESSs) syndrome is an idiosyncratic drug-induced reaction that rarely occurs in children but can lead to serious complications. It manifests most commonly with fever, extensive skin eruptions, and eosinophilia. Symptoms typically develop two to six weeks after the initiation of the inciting drug. Visceral organ involvement especially the liver can also occur and if not recognized early and the inciting drug is not stopped immediately, it can lead to liver failure. Therefore, early diagnosis is important but can be very challenging because of disease rarity, lack of a diagnostic test, and its overlap with other common pediatric allergic and infectious conditions. Case Presentation. A 2.5-year-old boy with known diagnosis of cystic fibrosis, bilateral bronchiectasis, pancreatic insufficiency, and chronic airway colonization with Pseudomonas aeruginosa was admitted to our hospital with acute pulmonary exacerbation of CF lung disease. He was treated with intravenous piperacillin-tazobactam and intravenous amikacin in addition to airway clearance. On day 18 of treatment, the patient developed high grade fever followed by diffuse erythematous and pruritic maculopapular rash. Blood tests showed high eosinophilia, high C-reactive protein (CRP), and high liver enzymes levels. The clinical features and the laboratory findings were consistent with the DRESS syndrome. Therefore, all antibiotics were discontinued. Progressive resolution of the symptoms was observed within two days. Laboratory abnormalities were also normalized in the follow-up clinic visit 4 months later.

Conclusion: Our case demonstrates the importance of early recognition of the DRESS syndrome in children who develop fever and skin rashes with eosinophilia while undergoing long-term antibiotic treatment. Prompt discontinuation of the offending drug is the cornerstone therapy and results in the resolution of symptoms and prevention of serious complications.

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囊性纤维化儿童嗜酸性粒细胞增多和全身症状综合征的药物反应
背景:嗜酸性粒细胞增多和全身症状的药物反应(dress)综合征是一种特殊的药物引起的反应,很少发生在儿童中,但可导致严重的并发症。最常见的表现是发热、大面积皮肤出疹和嗜酸性粒细胞增多。症状通常在刺激性药物开始后两到六周出现。内脏器官受累,尤其是肝脏,也可能发生,如果不及早发现,不立即停止刺激药物,它可以导致肝功能衰竭。因此,早期诊断很重要,但由于疾病罕见,缺乏诊断测试,并且与其他常见的儿科过敏和感染性疾病重叠,因此可能非常具有挑战性。案例演示。一名确诊为囊性纤维化、双侧支气管扩张、胰腺功能不全和铜绿假单胞菌慢性气道定植的2.5岁男孩,因CF肺部疾病急性肺加重而入院。他接受静脉注射哌拉西林-他唑巴坦和静脉注射阿米卡星治疗,并清除气道。治疗第18天,患者出现高热,随后出现弥漫性红斑和瘙痒性斑疹。血液检查显示高嗜酸性粒细胞,高c反应蛋白(CRP)和高肝酶水平。临床特征和实验室检查结果与DRESS综合征一致。因此,停用了所有抗生素。观察到症状在两天内逐渐消退。在4个月后的随访中,实验室异常也正常。结论:我们的病例表明,在长期接受抗生素治疗的儿童中,早期识别伴有嗜酸性粒细胞增多的发烧和皮疹的DRESS综合征是非常重要的。及时停药是治疗的基础,有助于缓解症状和预防严重并发症。
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来源期刊
CiteScore
1.90
自引率
0.00%
发文量
14
审稿时长
15 weeks
期刊介绍: Case Reports in Immunology is a peer-reviewed, Open Access journal that publishes case reports and case series related to allergies, immunodeficiencies, autoimmune diseases, immune disorders, cancer immunology and transplantation immunology.
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