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破解密码:高铁蛋白负荷与鲑鱼色皮肤发作

Cracking the code: high ferritin load with Salmon-Colored skin episodes.

作者信息

Satyal Paraash, Sukhcharan Walia, Yakubov Neriy, Babu Benson

机构信息

Department of Hospital Medicine, Internal Medicine Wyckoff Medical Center, 374 Stockholm Street, Brooklyn, New York, 11237, United States.

Assistant Professor New York Medical College, 40 Sunshine Cottage Rd, Valhalla, NY 10595, United States.

出版信息

Oxf Med Case Reports. 2024 Aug 23;2024(8):omae092. doi: 10.1093/omcr/omae092. eCollection 2024 Aug.

DOI:10.1093/omcr/omae092
PMID:39184869
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11343824/
Abstract

A 37-year-old previously healthy male presented to the Emergency Department with a two-week history of intermittent fevers, joint pain, sore throat, and a diffuse salmon-colored rash. Examination revealed a pruritic rash with joint swelling and red spots in the oropharynx. Initial sepsis management was instituted, but subsequent investigations, including infectious, hematologic, and autoimmune workups, were inconclusive. Notably, elevated ferritin levels prompted consideration of life-threatening conditions like Hemophagocytic Lymphohistiocytosis, which was ultimately ruled out. Adult-onset Still's Disease (AOSD) emerged as the leading diagnosis following the exclusion of other potential causes. A skin biopsy was performed with non-specific findings and corticosteroid treatment led to significant improvement. This case illustrates the clinical decision-making process of diagnosing AOSD and highlights the potential utility of novel AI technology in dermatologic assessments.

摘要

一名37岁既往健康的男性因持续两周的间歇性发热、关节疼痛、咽痛和弥漫性鲑鱼色皮疹就诊于急诊科。检查发现有瘙痒性皮疹、关节肿胀和口咽部红点。开始进行了初步的脓毒症管理,但随后包括感染、血液学和自身免疫检查在内的各项检查均无定论。值得注意的是,铁蛋白水平升高促使考虑噬血细胞性淋巴组织细胞增生症等危及生命的疾病,最终排除了该诊断。在排除其他潜在病因后,成人斯蒂尔病(AOSD)成为主要诊断。进行了皮肤活检,结果无特异性,皮质类固醇治疗带来了显著改善。该病例说明了诊断AOSD的临床决策过程,并强调了新型人工智能技术在皮肤科评估中的潜在效用。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f58b/11343824/9ab8deb2a562/omae092f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f58b/11343824/9ab8deb2a562/omae092f1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/f58b/11343824/9ab8deb2a562/omae092f1.jpg

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本文引用的文献

1
Unveiling the Mystery of Adult-Onset Still's Disease: A Compelling Case Report.揭开成人斯蒂尔病之谜:一则引人注目的病例报告。
Life (Basel). 2024 Jan 29;14(2):195. doi: 10.3390/life14020195.
2
Principles, applications, and future of artificial intelligence in dermatology.人工智能在皮肤病学中的原理、应用及未来
Front Med (Lausanne). 2023 Oct 12;10:1278232. doi: 10.3389/fmed.2023.1278232. eCollection 2023.
3
Treatment of adult-onset Still's disease: a review.成人斯蒂尔病的治疗:综述。
Ther Clin Risk Manag. 2014 Dec 22;11:33-43. doi: 10.2147/TCRM.S64951. eCollection 2015.
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Hemophagocytic lymphohistiocytosis: review of etiologies and management.噬血细胞性淋巴组织细胞增生症:病因及治疗综述
J Blood Med. 2014 Jun 12;5:69-86. doi: 10.2147/JBM.S46255. eCollection 2014.
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[Articular manifestations of adult Still's disease].[成人斯蒂尔病的关节表现]
Tunis Med. 2003 Apr;81(4):245-9.
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Hyperferritinemia in adult onset Still's disease and the hemophagocytic syndrome.成人斯蒂尔病和噬血细胞综合征中的高铁蛋白血症。
J Rheumatol. 1992 Sep;19(9):1425-7.