Unusual fungal infection of conidiobolomycosis presenting as nasal tumor – A

S. Agale, Vanita Rathi, Monica Tandale
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Abstract

Conidiobolomycosis is an unusual chronic subcutaneous fungal infection belonging to the order Entomophthorales of zygomycetes. It commonly affects the upper respiratory tract, mucous membranes of the upper lip, and subcutaneous tissues. Clinically, it presents as painless woody swelling commonly affecting the rhinofacial region causing extensive facial deformity. Due to its rarity and the lack of awareness, the diagnosis can be challenging. The definitive diagnosis of rhinofacial conidiobolomycosis is based on histopathological examination of skin lesions. The awareness of this entity is important for early diagnosis and patient management which helps in reducing morbidity associated with disease. We report a rare histopathologically diagnosed case of conidiobolomycosis in a 17-year-old male which was clinically considered a vascular tumor and radiologically diagnosed as hemangioma.
以鼻腔肿瘤为表现的异常真菌感染--A
子囊菌病(Conidiobolomycosis)是一种不常见的慢性皮下真菌感染,属于子囊菌中的 Entomophthorales 目。它常见于上呼吸道、上唇粘膜和皮下组织。在临床上,它表现为无痛性木质肿胀,通常影响鼻面部区域,导致面部大面积畸形。由于其罕见性和缺乏认识,诊断可能具有挑战性。鼻面部念珠菌病的明确诊断要以皮肤病变的组织病理学检查为基础。对这种疾病的认识对于早期诊断和患者管理非常重要,有助于降低与疾病相关的发病率。我们报告了一例罕见的组织病理学诊断病例,患者是一名17岁的男性,临床上被认为是血管瘤,放射学诊断为血管瘤。
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