An unusually severe case of shiitake mushroom dermatitis with features of drug reaction with eosinophilia and systemic symptoms.

Q3 Medicine
Skin health and disease Pub Date : 2025-01-20 eCollection Date: 2025-02-01 DOI:10.1093/skinhd/vzae012
Tristen Tze Wei Ng, Benjamin Andrew Wood, Patricia Le
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引用次数: 0

Abstract

Shiitake mushroom dermatitis is a well-documented phenomenon in the literature seen after consuming raw or undercooked shiitake mushrooms (Lentinus edodes). However, systemic features resembling a drug reaction with eosinophilia and systemic symptoms (DRESS) are rare. We report a case of severe shiitake mushroom dermatitis with atypical systemic features resembling DRESS. A 51-year-old man presented with acute unilateral periorbital oedema and flagellate erythema with no obvious drug precipitants and was initially managed as allergic contact dermatitis in the emergency department. Further inquiry revealed a history of raw shiitake mushroom ingestion 48 h before the onset of symptoms, which led to a working diagnosis of shiitake mushroom dermatitis. Skin biopsies showed mixed spongiotic and interface inflammatory reactions with a perivascular lymphocytic infiltrate and marked eosinophilia supportive of shiitake mushroom dermatitis. Rheumatological causes of flagellate erythema and periorbital oedema were excluded from clinical and laboratory findings. The patient initially presented with apyrexia and mild eosinophilia but then developed pyrexia, hypereosinophilia, neutrophilia and transaminitis. He subsequently developed bilateral periorbital oedema with his flagellate erythema, both of which were resolved with topical and oral corticosteroids. However, there was a new widespread morbilliform eruption with dorsal oedema of his hands. A diagnosis of DRESS-like shiitake mushroom dermatitis was considered. The patient required a long course of oral prednisolone to achieve clinical and biochemical resolution of his symptoms. Our case underscores the importance of prompt recognition and management of shiitake dermatitis, especially when it presents with DRESS-like features.

异常严重的香菇皮炎病例,以嗜酸性粒细胞增多和全身症状为特征的药物反应。
香菇皮炎是一种文献记载的现象,在食用生的或未煮熟的香菇(香菇)后出现。然而,类似于嗜酸性粒细胞增多和全身症状(DRESS)的药物反应的全身性特征是罕见的。我们报告一例严重的香菇皮炎,具有非典型的全身特征,类似DRESS。51岁男性,急性单侧眼眶周围水肿和鞭毛状红斑,无明显药物沉淀,最初作为过敏性接触性皮炎在急诊科就诊。进一步调查显示,在症状发作前48小时有生香菇摄入史,这导致了香菇皮炎的有效诊断。皮肤活检显示混合性海绵状和界面炎症反应,伴有血管周围淋巴细胞浸润和明显的嗜酸性粒细胞增多,支持香菇皮炎。风湿病引起的鞭毛状红斑和眶周水肿被排除在临床和实验室结果之外。患者最初表现为缺氧和轻度嗜酸性粒细胞增多,但随后发展为发热、嗜酸性粒细胞增多、中性粒细胞增多和转氨炎。随后,患者出现双侧眶周水肿并伴有鞭毛状红斑,这两种情况均经局部和口服皮质类固醇治疗。然而,有一个新的广泛的麻疹型爆发与手背水肿。考虑诊断为DRESS-like香菇皮炎。患者需要长期口服强的松龙以达到临床和生化症状的缓解。我们的病例强调了及时识别和处理香菇皮炎的重要性,特别是当它呈现出dress样特征时。
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
CiteScore
1.70
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0.00%
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审稿时长
10 weeks
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