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史蒂文斯-约翰逊综合征:一个令人困惑的诊断。

Stevens-Johnson Syndrome: A Perplexing Diagnosis.

作者信息

Dutt Jonathan, Sapra Amit, Sheth-Dutt Pooja, Bhandari Priyanka, Gupta Supriya

机构信息

Family and Community Medicine, Southern Illinois University School of Medicine, Springfield, USA.

Family Medicine, Southern Illinois University School of Medicine, Springfield, USA.

出版信息

Cureus. 2020 Mar 23;12(3):e7374. doi: 10.7759/cureus.7374.

Abstract

Stevens-Johnson syndrome/toxic epidermal necrolysis is a spectrum of mucocutaneous reactions that can occur due to drug reactions, infections with Mycoplasma pneumonia, human immunodeficiency virus (HIV), cancer, and genetics. Stevens-Johnson syndrome involves less than 10% of the body surface, while toxic epidermal necrolysis involves greater than 30%. The most common site of the lesions is mucocutaneous surfaces such as the eyes and oral cavity. Our patient was a 44-year-old female who presented to the emergency department with concerns for pain in her eyes, hands and feet, rash, and sore throat. Her rash worsened during the initial hospitalization. This case emphasizes the importance of pattern recognition of Stevens-Johnson syndrome, as this is a rare but serious condition that must be recognized and treated appropriately. The reaction is most commonly due to medications; however, a thorough history and physical exam are vital to diagnosing this potentially fatal condition.

摘要

史蒂文斯-约翰逊综合征/中毒性表皮坏死松解症是一系列可由药物反应、肺炎支原体感染、人类免疫缺陷病毒(HIV)、癌症和遗传因素引起的皮肤黏膜反应。史蒂文斯-约翰逊综合征累及的体表面积小于10%,而中毒性表皮坏死松解症累及的体表面积大于30%。最常见的病变部位是眼和口腔等皮肤黏膜表面。我们的患者是一名44岁女性,因眼睛、手脚疼痛、皮疹和喉咙痛到急诊科就诊。在初次住院期间,她的皮疹恶化。本病例强调了史蒂文斯-约翰逊综合征模式识别的重要性,因为这是一种罕见但严重的疾病,必须得到正确的识别和治疗。这种反应最常见的原因是药物;然而,全面的病史和体格检查对于诊断这种潜在的致命疾病至关重要。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/4722/7176330/1e4ba717f41e/cureus-0012-00000007374-i01.jpg

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