Kim Stanley, Chen Kevin, Stull William
Division of Hematology-Oncology, Department of Medicine, Kern Medical Center, Bakersfield, CA, USA.
Western University of Health Science-College of Osteopathic Medicine of the Pacific, Pomona, CA, USA.
J Med Case Rep. 2025 May 29;19(1):257. doi: 10.1186/s13256-025-05321-z.
Drug rash with eosinophilia and systemic symptoms syndrome is a severe T-cell-mediated adverse drug reaction characterized by a skin rash, fever, hematologic abnormalities, and internal organ involvement following prolonged exposure to a causative medication. Drugs associated with drug rash with eosinophilia and systemic symptoms syndrome include anticonvulsants, allopurinol, antibiotics, and nonsteroidal anti-inflammatory drugs. Fluconazole is an exceedingly rare cause of drug rash with eosinophilia and systemic symptoms syndrome, with only one previously reported case in abstract form. We present a case of a woman with pulmonary coccidioidomycosis who developed fluconazole-induced drug rash with eosinophilia and systemic symptoms syndrome, presenting with an unusual clinical feature.
A 19-year-old Hispanic woman was taking fluconazole for pulmonary coccidioidomycosis. A total of 30 days after starting fluconazole, she developed a generalized skin rash. Despite this, she continued taking the medication. Then 1 week later, she experienced facial swelling and a sensation of "throat closing." She also developed fever, axillary lymphadenopathy, eosinophilia, atypical lymphocytes, and hepatitis. Fluconazole was discontinued, and she was treated with intravenous methylprednisolone, which led to an overall improvement in her condition. During hospitalization, her antifungal therapy was switched to posaconazole. However, within 24 hours, she again experienced the "throat closing" sensation, which was relieved with an epinephrine injection. The patient was discharged on Day 6 with oral methylprednisolone. Again, 9 days after discharge, her symptoms recurred, including facial swelling and new skin rashes. She was readmitted and treated with famotidine, corticosteroids, and diphenhydramine. Her general condition and skin rashes gradually improved, with complete resolution of the rash 3 months after the initial eruption.
We present a case of a woman with pulmonary coccidioidomycosis who developed drug rash with eosinophilia and systemic symptoms syndrome induced by fluconazole. Our case meets Bocquet's diagnostic criteria and is categorized as "definite" drug rash with eosinophilia and systemic symptoms by the Registry of Severe Cutaneous Adverse Reactions. Drug rash with eosinophilia and systemic symptoms syndrome is a T-cell-mediated type IV hypersensitivity reaction; however, our patient also exhibited a unique symptom-a sensation of "throat closing"-suggestive of angioedema and a Type I hypersensitivity component. This symptom appeared while she continued fluconazole after the onset of drug rash with eosinophilia and systemic symptoms syndrome and recurred upon the initiation of posaconazole. Although both fluconazole and posaconazole belong to the triazole antifungal class, true allergic cross-reactivity medicated by IgE is rare probably due to their structural differences. This suggests cross-reactivity may occur even with structurally unrelated drugs in drug rash with eosinophilia and systemic symptoms syndrome. Clinicians managing suspected cases of drug rash with eosinophilia and systemic symptoms syndrome should promptly discontinue the offending drug and exercise caution when prescribing alternative medications to minimize the risk of further hypersensitivity reactions.
药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征是一种严重的T细胞介导的药物不良反应,其特征为在长期接触致病药物后出现皮疹、发热、血液学异常及内脏器官受累。与药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征相关的药物包括抗惊厥药、别嘌醇、抗生素及非甾体抗炎药。氟康唑是药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征极为罕见的病因,此前仅有1例以摘要形式报道的病例。我们报告1例患有肺球孢子菌病的女性,其发生了氟康唑诱发的药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征,并呈现出不寻常的临床特征。
一名19岁的西班牙裔女性因肺球孢子菌病正在服用氟康唑。开始服用氟康唑30天后,她出现了全身性皮疹。尽管如此,她仍继续服用该药物。1周后,她出现面部肿胀及“喉咙发紧”的感觉。她还出现发热、腋窝淋巴结肿大、嗜酸性粒细胞增多、非典型淋巴细胞及肝炎。停用氟康唑,并给予静脉注射甲泼尼龙治疗,这使她的病情总体得到改善。住院期间,她的抗真菌治疗改为泊沙康唑。然而,在24小时内,她再次出现“喉咙发紧”的感觉,注射肾上腺素后症状缓解。患者于第6天出院,口服甲泼尼龙。出院9天后,她的症状再次出现,包括面部肿胀和新的皮疹。她再次入院,接受法莫替丁、皮质类固醇和苯海拉明治疗。她的一般状况和皮疹逐渐改善,皮疹在初次发作3个月后完全消退。
我们报告1例患有肺球孢子菌病的女性,其发生了由氟康唑诱发的药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征。我们的病例符合博凯的诊断标准,并被严重皮肤不良反应登记处归类为“确诊”的药物性皮疹伴嗜酸性粒细胞增多和全身症状。药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征是一种T细胞介导的IV型超敏反应;然而,我们的患者还表现出一种独特症状——“喉咙发紧”的感觉,提示血管性水肿和I型超敏反应成分。这种症状在她出现药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征后继续服用氟康唑时出现,并在开始使用泊沙康唑时复发。尽管氟康唑和泊沙康唑都属于三唑类抗真菌药,但由IgE介导的真正过敏交叉反应可能很少见,可能是由于它们的结构差异。这表明在药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征中,即使是结构不相关的药物也可能发生交叉反应。处理疑似药物性皮疹伴嗜酸性粒细胞增多和全身症状综合征病例的临床医生应立即停用致病药物,并在开具替代药物时谨慎行事,以尽量降低进一步超敏反应的风险。