Patra Pratap K, Banday Aaqib Z, Jindal Ankur K, Bhattarai Dharmagat, Patra Nilamani, Saikia Uma N, Gupta Anju, Suri Deepti
Allergy Immunology Unit, Department of Pediatrics, Advanced Pediatrics Centre, Research Block-A, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
Department of Pathology, Research Block-A, Post Graduate Institute of Medical Education and Research (PGIMER), Chandigarh, India.
J Family Med Prim Care. 2022 Jun;11(6):3280-3286. doi: 10.4103/jfmpc.jfmpc_1031_21. Epub 2022 Jun 30.
Drug reaction with eosinophilia and systemic symptoms (DRESS) syndrome after the use of first-line antitubercular drugs (ATDs) is rare and literature regarding DRESS syndrome due to ATDs is scarce in children. We report a young boy with tuberculosis who developed DRESS syndrome after exposure to isoniazid. A 9-year-old boy, diagnosed clinically as pulmonary tuberculosis, presented with fever, fast breathing, maculopapular rash, and one episode of gross hematuria. He had been on 4-drug ATD therapy (isoniazid, rifampicin, ethambutol, and pyrazinamide) for the past 4 weeks. In view of multiorgan involvement and absence of a microbiological diagnosis of tuberculosis, vasculitis was considered and he was treated with steroids. As the child recovered, both corticosteroids and ATD therapy were stopped. At 6 months of follow-up, he was presented with pneumonia. Microbiological diagnosis of tuberculosis was made and 4-drug ATD therapy was reinitiated. After 15 days, he again developed a high-grade fever and rash. On evaluation, isoniazid-induced DRESS syndrome was diagnosed. Subsequently, he received a modified regimen of ethambutol, pyrazinamide, levofloxacin, and linezolid. DRESS syndrome did not recur on these ATDs and the child became asymptomatic. Linezolid was stopped after 3 months of therapy and ethambutol, pyrazinamide, and levofloxacin are being continued. Currently, he has completed 15 months of modified ATD therapy. As a high index of suspicion is required for early diagnosis and management that are crucial to reducing morbidity and mortality, DRESS syndrome should be among the differentials in children with unexplained febrile illnesses.
使用一线抗结核药物(ATD)后发生的伴有嗜酸性粒细胞增多和全身症状的药物反应(DRESS)综合征很罕见,关于儿童因ATD导致DRESS综合征的文献也很匮乏。我们报告了一名患有结核病的小男孩,在接触异烟肼后发生了DRESS综合征。一名9岁男孩,临床诊断为肺结核,出现发热、呼吸急促、斑丘疹和一次肉眼血尿。在过去4周里,他一直在接受4种药物的抗结核治疗(异烟肼、利福平、乙胺丁醇和吡嗪酰胺)。鉴于多器官受累且缺乏结核病的微生物学诊断,考虑为血管炎,并对他进行了类固醇治疗。随着孩子康复,停用了皮质类固醇和抗结核治疗。在随访6个月时,他出现了肺炎。进行了结核病的微生物学诊断,并重新开始了4种药物的抗结核治疗。15天后,他再次出现高热和皮疹。经评估,诊断为异烟肼诱发的DRESS综合征。随后,他接受了乙胺丁醇、吡嗪酰胺、左氧氟沙星和利奈唑胺的改良治疗方案。在这些抗结核药物治疗期间,DRESS综合征未复发,孩子也没有症状了。治疗3个月后停用了利奈唑胺,继续使用乙胺丁醇、吡嗪酰胺和左氧氟沙星。目前,他已经完成了15个月的改良抗结核治疗。由于早期诊断和管理对于降低发病率和死亡率至关重要,需要高度怀疑,DRESS综合征应列入不明原因发热疾病儿童的鉴别诊断之中。