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一名患有复杂自身免疫性疾病的儿科患者中,碘与甲巯咪唑所致中毒性表皮坏死松解症的比较

Toxic Epidermal Necrolysis Secondary to Iodine Versus Methimazole in a Pediatric Patient With Complex Autoimmune Disease.

作者信息

Smaha Katlyn M, Prosser John D, Chan Jacqueline T

机构信息

Pediatric Endocrinology, Medical College of Georgia at Augusta University, Augusta, USA.

Pediatric Otolaryngology, Head and Neck Surgery, Medical College of Georgia at Augusta University, Augusta, USA.

出版信息

Cureus. 2024 Apr 4;16(4):e57618. doi: 10.7759/cureus.57618. eCollection 2024 Apr.

Abstract

We report a case of a 17-year-old girl who developed toxic epidermal necrolysis (TEN) secondary to preoperative iodine administration before thyroidectomy for Graves' disease. Past medical history was significant for COVID-19 and multisystem inflammatory syndrome in Children (MISC-C), with subsequent diagnoses of type 1 diabetes mellitus (T1DM), Addison disease, and Graves' disease. Her Graves disease was initially managed with methimazole. While there are reported cases of Stevens-Johnson syndrome (SJS) and TEN due to methimazole, the patient had discontinued methimazole over one month prior. Therefore, she likely represents the first case of TEN reported secondary to potassium iodide solution in a pediatric patient. Given the rarity of TEN in pediatric patients, our case highlights the challenges in managing complex autoimmune conditions and underscores the importance of careful medication choices in such cases.

摘要

我们报告了一例17岁女孩的病例,该女孩在因格雷夫斯病进行甲状腺切除术之前接受术前碘给药后发生了中毒性表皮坏死松解症(TEN)。既往病史包括新冠病毒病和儿童多系统炎症综合征(MISC-C),随后诊断为1型糖尿病(T1DM)、艾迪生病和格雷夫斯病。她的格雷夫斯病最初用甲巯咪唑治疗。虽然有因甲巯咪唑导致史蒂文斯-约翰逊综合征(SJS)和TEN的报道病例,但该患者在一个多月前就已停用甲巯咪唑。因此,她可能是儿科患者中首例因碘化钾溶液继发TEN的报道病例。鉴于TEN在儿科患者中罕见,我们的病例突出了管理复杂自身免疫性疾病的挑战,并强调了在此类病例中谨慎选择药物的重要性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7550/11069421/2c87c76af892/cureus-0016-00000057618-i01.jpg

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