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帕博利珠单抗治疗后发生药物性Sweet综合征1例罕见病例

A Rare Case of Drug-Induced Sweet Syndrome After Pembrolizumab Therapy.

作者信息

Muralidharan Suchitra, Mariano Andrew T, Joshi Dhruv, Andrews Trisha E, Liu Seban, Basha Ahsan, Huynh Nha

机构信息

Internal Medicine, Riverside Medical Center, Kankakee, USA.

Cardiology, Riverside Medical Center, Kankakee, USA.

出版信息

Cureus. 2024 Jun 9;16(6):e62027. doi: 10.7759/cureus.62027. eCollection 2024 Jun.

Abstract

Sweet syndrome is an uncommon inflammatory disorder characterized by the abrupt appearance of painful, erythematous papules, plaques, or nodules on the skin. Fever and leukocytosis frequently accompany the cutaneous lesions. In addition, involvement of the eyes, musculoskeletal system, and internal organs may occur. Sweet syndrome has been associated with a broad range of disorders. There are three subtypes: classical Sweet syndrome, malignancy-associated Sweet syndrome, and drug-induced Sweet syndrome. Classical Sweet syndrome is not associated with malignancy or drugs. It is essentially associated with an upper respiratory infection, gastrointestinal infection, inflammatory bowel disease, and pregnancy. Malignancy-associated Sweet syndrome is associated with hematologic malignancy more than solid malignancy, most commonly with acute myeloid leukemia. Drug-induced Sweet syndrome usually develops approximately two weeks after drug exposure, in patients who lack a prior history of exposure to the inciting drug. Here we are discussing our patient, a 68-year-old male who presented eight weeks after starting chemotherapy with pemetrexed, carboplatin, and pembrolizumab for left lung adenocarcinoma with macular rash. On further investigation with biopsy was found to have neutrophilic dermatitis, hence being diagnosed with drug-induced Sweet syndrome. Histopathology revealed a dermis with infiltration of neutrophils with lekocytoclasia.

摘要

斯威特综合征是一种罕见的炎症性疾病,其特征为皮肤上突然出现疼痛性红斑丘疹、斑块或结节。发热和白细胞增多症常伴随皮肤病变。此外,眼睛、肌肉骨骼系统和内脏器官也可能受累。斯威特综合征与多种疾病有关。它有三种亚型:经典型斯威特综合征、恶性肿瘤相关型斯威特综合征和药物诱导型斯威特综合征。经典型斯威特综合征与恶性肿瘤或药物无关。它主要与上呼吸道感染、胃肠道感染、炎症性肠病和妊娠有关。恶性肿瘤相关型斯威特综合征与血液系统恶性肿瘤的关联大于实体恶性肿瘤,最常见于急性髓系白血病。药物诱导型斯威特综合征通常在接触药物后约两周出现,见于既往无诱发药物接触史的患者。在此我们讨论我们的患者,一名68岁男性,在开始使用培美曲塞、卡铂和帕博利珠单抗治疗左肺腺癌并出现斑疹八周后就诊。经活检进一步检查发现有嗜中性皮病,因此被诊断为药物诱导型斯威特综合征。组织病理学显示真皮有嗜中性粒细胞浸润并伴有核碎裂。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7b74/11163154/12d206c4161f/cureus-0016-00000062027-i01.jpg

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