Giant cellulitis-like Sweet syndrome mimicking cellulitis: a case report.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL
Selamawit T Muche, Lishan D Tefera, Nigatu A Gerba, Kibrom M Gebremedhin, Abdusamed A Abdusamed, Melkamu K Nidaw, Abenezer A Kebede, Edom T Degefa
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引用次数: 0

Abstract

Background: Sweet syndrome (acute febrile neutrophilic dermatosis) is an uncommon inflammatory disorder characterized by the abrupt appearance of painful, edematous, and erythematous papules, plaques, or nodules on the skin. There are various subtypes, such as classical, drug-induced, malignancy-associated, and the less common variant giant cellulitis-like Sweet syndrome. This case is unique due to its presentation of the giant cellulitis-like variant of Sweet syndrome in a patient from Ethiopia. The unusual distribution of the skin lesions and the initial lack of response to antibiotics make this case particularly noteworthy. It underscores the importance of considering Sweet syndrome in differential diagnoses when faced with atypical skin manifestations and ineffective antibiotic treatment. This contribution adds valuable insights to the scientific literature by highlighting the need for heightened awareness of this rare variant and improving diagnostic accuracy in similar clinical scenarios.

Case presentation: A 60-year-old Ethiopian male patient who presented to the accident and emergency department with a 5-day history of fever, chills, sweating, and rigor accompanied by a reddish skin color change around the anterolateral region of the right chest wall. On physical examination, there were erythematous, indurated tender plaques with ill-defined borders over the right antero- and posterolateral chest wall with extension to the lateral part of the right neck and medial aspect of the right arm. Subsequently, the patient was started on antibiotics, but there was a suboptimal response. Skin biopsy revealed features suggestive of giant cellulitis-like Sweet syndrome. He was then started on steroids, which significantly improved his symptoms.

Conclusion: A cautious stance is essential when identifying Sweet syndrome in individuals displaying erythematous plaque-like skin lesions in atypical areas of the body with uneven distribution. Such presentation may signal Sweet syndrome rather than a common infection. If conventional treatments, such as antibiotics, fail to resolve symptoms, consider Sweet syndrome as a potential diagnosis. This approach ensures timely and appropriate treatment, preventing treatment delay and misdiagnosis.

模仿蜂窝组织炎的巨大蜂窝组织炎样斯威特综合征:病例报告。
背景介绍斯威特综合征(急性发热性嗜中性粒细胞皮肤病)是一种不常见的炎症性疾病,其特征是皮肤上突然出现疼痛、水肿和红斑丘疹、斑块或结节。该病有多种亚型,如传统型、药物诱发型、恶性肿瘤相关型和较少见的变异型巨大蜂窝织炎样斯威特综合征。本病例的独特之处在于,患者是一名来自埃塞俄比亚的斯威特综合征巨型蜂窝织炎样变异型患者。由于皮损分布不寻常,且最初对抗生素无反应,因此本病例尤其值得注意。它强调了在面对非典型皮肤表现和抗生素治疗无效时,在鉴别诊断中考虑斯威特综合征的重要性。这篇论文为科学文献增添了有价值的见解,强调需要提高对这种罕见变异的认识,并提高类似临床情况下的诊断准确性:一名 60 岁的埃塞俄比亚男性患者因发热、寒战、出汗和僵硬 5 天,伴有右胸壁前外侧周围皮肤颜色变红而到急诊科就诊。体格检查时发现,患者右胸壁前外侧和后外侧出现边界不清的红斑、凹陷性压痛斑块,并向右颈外侧和右臂内侧扩展。随后,患者开始使用抗生素,但反应不佳。皮肤活检结果显示,该病的特征提示为巨大蜂窝织炎样斯威特综合征。随后,他开始服用类固醇药物,症状明显好转:结论:对于身体非典型部位出现红斑样皮损且分布不均的患者,在鉴别斯威特综合征时必须持谨慎态度。这种表现可能预示着斯威特综合征而非普通感染。如果抗生素等常规治疗无法缓解症状,应考虑将斯威特综合征作为潜在诊断。这种方法可确保及时、适当的治疗,防止延误治疗和误诊。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
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来源期刊
Journal of Medical Case Reports
Journal of Medical Case Reports Medicine-Medicine (all)
CiteScore
1.50
自引率
0.00%
发文量
436
期刊介绍: JMCR is an open access, peer-reviewed online journal that will consider any original case report that expands the field of general medical knowledge. Reports should show one of the following: 1. Unreported or unusual side effects or adverse interactions involving medications 2. Unexpected or unusual presentations of a disease 3. New associations or variations in disease processes 4. Presentations, diagnoses and/or management of new and emerging diseases 5. An unexpected association between diseases or symptoms 6. An unexpected event in the course of observing or treating a patient 7. Findings that shed new light on the possible pathogenesis of a disease or an adverse effect
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