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接触放射性造影剂后出现大疱性皮疹和急性肾损伤:Sweet综合征。

Acute Onset of Bullous Skin Rash and Acute Kidney Injury after Exposure to Radiocontrast: Sweet's Syndrome.

作者信息

Abdelnabi Mahmoud, Cavazos Annia, Thongpiya Jerapas, Pruneda Corley, Yingchoncharoen Pitchaporn, Sullivan Sierra, Davalos Jesus, Tarbox Michelle

机构信息

Internal Medicine Department, Texas Tech University Health Science Center, Lubbock, Texas, USA.

Dermatology Department, Texas Tech University Health Sciences Center, Lubbock, Texas, USA.

出版信息

Eur J Case Rep Intern Med. 2023 Mar 13;10(4):003781. doi: 10.12890/2023_003781. eCollection 2023.

Abstract

UNLABELLED

Sweet's syndrome or acute febrile neutrophilic dermatosis is characterized by an acute inflammatory skin eruption of oedematous and erythematous papules, plaques or nodules, accompanied by fever, and leucocytosis with possible extracutaneous involvement. Aetiologies include infections, inflammatory bowel disease, pregnancy or malignancy, or the syndrome may be drug-induced by many classes of medications or very rarely, radiocontrast exposure. Herein, the authors report a case of radiocontrast-induced bullous Sweet's syndrome and contrast-induced acute kidney injury in a woman in her 60s with a complex medical history.

LEARNING POINTS

Patients with Sweet's syndrome (SS) typically present with acute-onset fever, leucocytosis, and erythematous, tender plaques with dense neutrophilic infiltration in the dermis. The condition is classified into three subtypes: classic SS, malignancy-associated SS, and drug-induced SS.Drug-induced SS is characterized by an abrupt onset of a painful erythematous rash, dense neutrophilic dermal infiltrate without vasculitis, a temporal relationship between exposure and onset, and resolution of symptoms after drug discontinuation and/or corticosteroid therapy.Treatment options include systemic corticosteroids as first-line therapy, while colchicine, dapsone, indomethacin, naproxen, clofazimine, ciclosporin, α-interferon, and potassium iodide may be considered as second-line therapies in cases resistant to corticosteroids.

摘要

未标注

斯威特综合征或急性发热性嗜中性皮病的特征是出现水肿性红斑丘疹、斑块或结节的急性炎症性皮肤疹,伴有发热、白细胞增多,可能累及皮肤外。病因包括感染、炎症性肠病、妊娠或恶性肿瘤,或者该综合征可能由多种药物引起,或非常罕见地由放射造影剂暴露引起。在此,作者报告了一例60多岁有复杂病史的女性发生放射造影剂诱发的大疱性斯威特综合征和造影剂诱发的急性肾损伤的病例。

学习要点

斯威特综合征(SS)患者通常表现为急性发热、白细胞增多,以及真皮内有密集嗜中性粒细胞浸润的红斑性压痛斑块。该病症分为三种亚型:经典型SS、恶性肿瘤相关型SS和药物诱发型SS。药物诱发型SS的特征是疼痛性红斑皮疹突然发作、真皮内有密集嗜中性粒细胞浸润而无血管炎、暴露与发作之间存在时间关系,以及停药和/或使用皮质类固醇治疗后症状缓解。治疗选择包括全身性皮质类固醇作为一线治疗,而秋水仙碱、氨苯砜、吲哚美辛、萘普生、氯法齐明、环孢素、α干扰素和碘化钾在对皮质类固醇耐药的病例中可作为二线治疗药物。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a93e/10084799/aca4fe0ef9b0/3781_fig01.jpg

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