皮下担子球菌病:一种罕见的真菌在免疫能力的儿童,证明抗真菌治疗的持续时间较长

Kiruthiga K.G, Prachi Sharma, Aparna M. Joshi, A. Pradhan, M. Otiv
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引用次数: 0

摘要

摘要皮下担子孢子菌病是一种由环境腐生植物担子孢子引起的罕见真菌感染。该病见于18个月至80岁的免疫功能正常的个体,在儿童中更为常见。我们报告一例来自马哈拉施特拉邦艾哈迈德纳格尔的10岁免疫功能男性儿童的皮下担子球菌病,其主诉为右臀肌无触痛,弥漫性肿胀,逐渐累及大腿内侧和背部。复盖皮肤色素沉着,局部有鳞屑。它与行走困难和排尿有关。给患者开了多种药物,但没有记录。所有的初步调查都是与组织病理学的深切口活检一起完成的。MRI提示?淋巴管瘤吗?血管畸形。组织病理学显示泛膜炎伴密集的嗜酸性粒细胞聚集。少量宽的、无菌的真菌菌丝隐藏在炎性浸润中,被splendohoeppli现象所包围。患者口服氟康唑治疗一年,症状完全缓解。经过一年的随访,患者临床表现良好。临床表现为皮肤和皮下组织硬化,类似软组织肉瘤。然而,组织病理学检查确定了诊断。真菌感染在免疫抑制患者中很常见,在儿童中极为罕见。由于这是一种罕见的真菌感染,可见于免疫能力的儿童和年轻人,它往往被忽视作为鉴别诊断。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Subcutaneous basidiobolomycosis: An unusual fungus in immuno-competent children, vindicating longer duration of anti-fungal treatment
Subcutaneous Basidiobolomycosis is a rare fungal infection caused by environmental saprophyte Basidiobolus ranarum. The disease is seen among immunocompetent individuals of age 18 months to 80 years, being more common in children. We report a case of Subcutaneous Basidiobolomycosis in a 10-year-old immunocompetent male child from Ahmednagar, Maharashtra who presented with complaints of right gluteal non tender, diffuse swelling, which was gradually progressive involving inner and back of thigh. The overlying skin was hyperpigmented with scaling at places. It was associated with complaints of difficulty in walking and voiding of urine. Patient was prescribed multiple medicines with no records available. All primary investigations were done along with a deep incisional biopsy for histopathology. MRI was suggestive of? lymphangioma? vascular malformation. Histopathology revealed panniculitis with dense collections of eosinophils. Few broad, aseptate fungal hyphae were seen camouflaged within the inflammatory infiltrate, surrounded by Splendore-Hoeppli phenomenon. The patient was treated with oral fluconazole for a period of one year with complete resolution of the symptoms. After one year of follow-up, the patient is clinically well. Clinically, this lesion presented as induration of skin and subcutaneous tissue thus mimicking a soft tissue sarcoma. However, histopathological examination clinched the diagnosis. Fungal infections are common in immuno-suppressed patients, and extremely uncommon in children. Since this is an exceptional rare fungal infection seen in immuno-competent children and young adults, it is often disregarded as a differential diagnosis.
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