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足菌肿:现状与展望

Eumicetoma: actualidades y perspectivas.

作者信息

Arenas Roberto, Vega-Mémije M ª Elisa, Rangel-Gamboa Lucía

机构信息

Sección de Micología Médica. Hospital General Dr. Manuel Gea González, Ciudad de México, México.

Subdirección de Investigación Biomédica. Hospital General Dr. Manuel Gea González, Ciudad de México, México.

出版信息

Gac Med Mex. 2017;153(7):841-851. doi: 10.24875/GMM.17002917.

DOI:10.24875/GMM.17002917
PMID:29414948
Abstract

The eumycetoma is a severely debilitating chronic progressive fungal cutaneous infection. Classic clinical triad is characterized by painless subcutaneous mass, sinus tracts formation and sero-purulent discharge that contain aggregates of fungal hyphae called grains. Any part of the body can have affected, with extension to muscular or bone, even visceral compromised. The eumycetoma is observed in tropical and subtropical countries; In Latin-America, is reported with less frequency. In endemic areas, antibody presence again etiological agents were higher compared with number of people affected, thus it is supposed that individual genetic susceptibility most by exist. Recently, it was reported specific polymorphism in genes CR1, IL-8, NOS2 and chitriosidase, which were associated with development of eumycetoma. The diagnosis is suggested by clinical presentation; the histopathology and microbiology studies, plus radiologic valuation confirmed diagnosis. Madurella mycetomatis is the most informed etiological agent. Using phylogenetic tools new species in genus Madurella were reported; moreover, Trematosphaeria grisea and Pseudallescheria boydii were reclassified. Etiological agent Identification is important, because differences in antifungal susceptibility exist. Eumycetoma treatment includes surgery plus antifungal drugs. Identification of etiological agents is primordial, because antifungal resistance could exist. To development new pharmacological strategies, comprehension of grain formation physiology and drugs effects are necessary.

摘要

足菌肿是一种严重致残的慢性进行性真菌性皮肤感染。典型的临床三联征表现为无痛性皮下肿块、窦道形成以及含有称为颗粒的真菌菌丝聚集体的浆液脓性分泌物。身体的任何部位都可能受累,并可扩展至肌肉或骨骼,甚至累及内脏。足菌肿在热带和亚热带国家较为常见;在拉丁美洲,其报道频率较低。在流行地区,针对病原体的抗体存在率高于患病人数,因此推测可能存在个体遗传易感性。最近,有报道称CR1、IL - 8、NOS2和壳三糖苷酶基因存在特定多态性,这些多态性与足菌肿的发生发展有关。根据临床表现可提出诊断;组织病理学和微生物学研究以及影像学评估可确诊。马杜拉足肿菌是最常见的病原体。利用系统发育工具报道了马杜拉属的新物种;此外,灰黑弯孢菌和波氏假阿利什霉也被重新分类。病原体鉴定很重要,因为不同病原体的抗真菌药敏性存在差异。足菌肿的治疗包括手术加抗真菌药物。病原体鉴定至关重要,因为可能存在抗真菌耐药性。为了开发新的药理策略,了解颗粒形成生理学和药物作用是必要的。

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