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A case report of recurrent Well's syndrome masquerading as cellulitis.

作者信息

Qureshi Anum, Manley Jasmine, Flack Tristan, Lowitt Mark H

机构信息

Department of Internal Medicine, Greater Baltimore Medical Center, Towson, MD, USA.

Division of Dermatology, Greater Baltimore Medical Center, Towson, MD, USA.

出版信息

J Community Hosp Intern Med Perspect. 2021 Nov 15;11(6):866-870. doi: 10.1080/20009666.2021.1979737. eCollection 2021.

DOI:10.1080/20009666.2021.1979737
PMID:34804409
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC8604493/
Abstract

Eosinophilic cellulitis (Well's syndrome) is a rare relapsing inflammatory disorder characterized by infiltration of eosinophils into the dermis. Although rare, WS should be considered in patients with a history of asthma and skin lesions that are resistant to antibiotic therapy. We report a case of recurrent WS. A 67-year-old woman with a history of asthma presented with a longstanding left pretibial ulcer with surrounding erythema, pain, and serous drainage, which had failed treatment with oral and parenteral antibiotics. Skin biopsy revealed eosinophilic cellulitis. Rapid improvement occurred with systemic steroid treatment; however, recurrent disease in the perineum developed as corticosteroids were tapered.

摘要
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/1eec94bceefa/ZJCH_A_1979737_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/5cea94627721/ZJCH_A_1979737_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/f7f678e2fb70/ZJCH_A_1979737_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/f8365af39145/ZJCH_A_1979737_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/1eec94bceefa/ZJCH_A_1979737_F0004_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/5cea94627721/ZJCH_A_1979737_F0001_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/f7f678e2fb70/ZJCH_A_1979737_F0002_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/f8365af39145/ZJCH_A_1979737_F0003_OC.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/7118/8604493/1eec94bceefa/ZJCH_A_1979737_F0004_OC.jpg

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本文引用的文献

1
Effective treatment with mepolizumab in a patient with refractory Wells syndrome.美泊利珠单抗成功治疗一名难治性威尔斯综合征患者。
J Dtsch Dermatol Ges. 2020 Jul;18(7):737-739. doi: 10.1111/ddg.14151.
2
Mepolizumab Therapy for Recalcitrant Eosinophilic Annular Erythema in an Adult: A Case Report and Review of Treatment Options.美泊利珠单抗治疗成人顽固性嗜酸性环状红斑:一例报告及治疗选择综述
Dermatol Ther (Heidelb). 2020 Aug;10(4):893-899. doi: 10.1007/s13555-020-00412-9. Epub 2020 Jun 23.
3
Eosinophilic cellulitis (Wells syndrome) successfully treated with mepolizumab.
美泊利单抗成功治疗嗜酸性粒细胞性蜂窝织炎(韦尔斯综合征)。
JAAD Case Rep. 2018 Jun 6;4(6):548-550. doi: 10.1016/j.jdcr.2018.02.011. eCollection 2018 Jul.
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Diagnosis and management of eosinophilic cellulitis (Wells' syndrome): A case series and literature review.嗜酸性粒细胞性蜂窝织炎(韦尔斯综合征)的诊断与管理:病例系列及文献综述
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Wells Syndrome with Multiorgan Involvement Mimicking Hypereosinophilic Syndrome.伴有多器官受累的韦尔斯综合征,酷似高嗜酸性粒细胞综合征。
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Wells' syndrome is a distinctive disease entity and not a histologic diagnosis.威尔斯综合征是一种独特的疾病实体,而非组织学诊断。
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