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[被误诊为细菌性蜂窝织炎的威尔斯综合征]

[Wells syndrome misdiagnosed as bacterial cellulitis].

作者信息

Kettani F, Baline K, Hali F, Azzouzi S, Chiheb S

机构信息

Service de dermatologie et vénéréologie, CHU de Ibn Rochd, Casablanca, Maroc.

Service de dermatologie et vénéréologie, CHU de Ibn Rochd, Casablanca, Maroc.

出版信息

Rev Med Interne. 2020 Jul;41(7):496-499. doi: 10.1016/j.revmed.2020.02.007. Epub 2020 Feb 20.

Abstract

Wells syndrome (WS), also called eosinophilic cellulitis is a rare inflammatory skin disease with about 200 cases reports in the literature. It is part of eosinophilic dermatoses and presents a diagnostic challenge. We report a case of WS presenting as bacterial cellulitis. A 59 year-old woman was referred to our department with a 10-day history of a rapidly extending erysipelatoid rash of the left upper limb, non-responding to oral antibiotics. Upon physical examination, erythema with swelling and blisters were found on the left upper limb with urticarial-like lesions on the breast, the belly and on the inner thighs. The patient was admitted with presumed bacterial cellulitis and was treated with intravenous ampicillin. Blood count showed raised eosinophils (2050/ul) along with a biological inflammatory syndrome. Biopsies were performed on both bullous and urticarial-like lesions showing perivascular and interstitial inflammatory infiltrate, made essentially of eosinophils with flame figures. The diagnosis of WS was made and the patient received local and oral corticosteroids (0,5mg/kg/d) with good evolution. The rarity and clinical manifestations of WS makes it sometimes difficult to differentiate between a WS and a bacterial cellulitis. However, biological and histological findings can help the clinician make the differential diagnosis between these two diseases for a better management.

摘要

韦尔斯综合征(WS),也称为嗜酸性粒细胞性蜂窝织炎,是一种罕见的炎症性皮肤病,文献中约有200例病例报告。它是嗜酸性粒细胞性皮肤病的一部分,诊断具有挑战性。我们报告一例表现为细菌性蜂窝织炎的WS病例。一名59岁女性因左上肢迅速扩展的丹毒样皮疹10天病史转诊至我科,口服抗生素治疗无效。体格检查发现左上肢有红斑、肿胀和水疱,乳房、腹部和大腿内侧有荨麻疹样损害。患者因疑似细菌性蜂窝织炎入院,接受静脉注射氨苄西林治疗。血常规显示嗜酸性粒细胞增多(2050/μl),伴有生物学炎症综合征。对水疱性和荨麻疹样损害均进行了活检,显示血管周围和间质炎症浸润,主要由嗜酸性粒细胞组成,并伴有火焰状图形。确诊为WS,患者接受局部和口服皮质类固醇(0.5mg/kg/d)治疗,病情好转。WS的罕见性和临床表现有时使其难以与细菌性蜂窝织炎相鉴别。然而,生物学和组织学检查结果有助于临床医生对这两种疾病进行鉴别诊断,以更好地进行治疗。

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