揭示足菌肿的挑战:一个突出诊断困境和治疗胜利的病例系列。

Q3 Medicine
Skin health and disease Pub Date : 2025-02-14 eCollection Date: 2025-02-01 DOI:10.1093/skinhd/vzae017
Mahesh Mathur, Neha Thakur, Sunil Jaiswal, Sandhya Regmi, Supriya Paudel
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引用次数: 0

摘要

足菌肿是一种常见于热带和亚热带地区的深部真皮和皮下组织的慢性化脓性肉芽肿感染,由丝状需氧细菌(放线菌瘤)或真真菌(真菌瘤)引起,分别占全球病例的60%和40%。病原微生物通过刺扎或反复创伤的接种,从受污染的土壤或植物物质进入皮下组织,通常是脚。它通常影响男性、农民和田间工人。鉴别真菌肿和放线菌肿具有挑战性,但在开始长期治疗前必须进行鉴别。我们的一名患者表现为大腿病变和非典型孢子毛样,而另外两名患者因真菌性肿接受了多年的抗真菌药物治疗,但没有适当的调查和改善。放线菌瘤的早期诊断是必要的,通过适当的调查检查、组织病理学和直接显微镜检查来防止组织破坏、骨侵犯和最终功能丧失。我们在此报告了3例放线菌瘤的临床和微生物学特征,根据Cochrane系统评价方案2018的建议,使用甲氧苄啶-磺胺甲恶唑和阿莫西林-克拉维酸联合叶酸片成功治疗。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Unravelling the challenges of mycetoma: a case series highlighting diagnostic dilemmas and therapeutic triumphs.

Mycetoma is a chronic suppurative granulomatous infection of the deep dermis and subcutaneous tissue prevalent in tropical and subtropical regions and is caused by filamentous aerobic bacteria (actinomycetoma) or true fungi (eumycetoma), representing 60% and 40% of cases worldwide, respectively. The causative organism enters into the subcutaneous tissue, usually of the foot, from contaminated soil or vegetative material through inoculation from a thorn prick, or repeated trauma. It commonly affects men, farmers and field workers. Differentiating eumycetoma from actinomycetoma can be challenging but is required before starting prolonged treatment. One of our patients presented with lesions on the thigh and in a sporotrichoid pattern that is atypical, while the other two patients were treated with antifungal medication for eumycetoma for years without proper investigation and improvement. Early diagnosis of actinomycetoma is mandatory to prevent tissue destruction, bone invasion and ultimate loss of function by proper investigative workup, histopathology and direct microscopy of discharge. We here report three cases of actinomycetoma with clinical and microbiology profiles treated successfully with tablets of trimethoprim-sulfamethoxazoleand amoxicillin-clavulanic acid along with folic acid as proposed by the Cochrane systemic review protocol 2018.

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CiteScore
1.70
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