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Majocchis Granuloma after Topical Corticosteroids Therapy

机译:局部糖皮质激素治疗后的马约奇肉芽肿

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摘要

Majocchi's granuloma (MG) is an unusual but not rare dermatophyte infection of dermal and subcutaneous tissues. Dermatophytes usually result in the infections of hair, epidermis, and nail, and are rarely involved in deep cutaneous and subcutaneous tissues. Now it is considered that MG includes two forms: one is a small perifollicular papular form and the other is a deep subcutaneous nodular form; the front one mainly occurs in healthy individuals and the latter one usually presents in immunocompromised hosts. The clinical manifestations of MG are many and varied, except the common presentations of erythema, papule and nodules, and Kaposi sarcoma-like and molluscum-like lesions have been reported in literatures (Kim et al. (2011), Bord et al. (2007), and Lillis et al. (2010)). This characteristic induces the difficulty of diagnosis, and thus it is so important and necessary to make direct microscopical and histological examinations. We describe a case of MG over the face in a patient who had been treated with topical corticosteroids over a long time.
机译:Majocchi肉芽肿(MG)是一种罕见但并非罕见的皮肤和皮下组织皮肤癣菌感染。皮肤癣菌通常导致头发,表皮和指甲的感染,很少涉及深层的皮肤和皮下组织。现在认为MG包括两种形式:一种是小毛囊周围小丘疹形式,另一种是深皮下结节状形式;另一种是深皮下结节形式。前一种主要存在于健康个体中,而后一种通常存在于免疫功能低下的宿主中。除红斑,丘疹和结节的常见表现外,MG的临床表现也多种多样,文献中已报道了卡波西肉瘤样和软体动物样病变(Kim等人(2011),Bord等人( 2007年)和Lillis等人(2010年)。该特征引起诊断的困难,因此进行直接的显微镜检查和组织学检查是如此重要和必要。我们描述了一名长时间接受局部糖皮质激素治疗的患者面部MG病例。

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