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首页> 外文期刊>Journal of Clinical and Diagnostic Research >A Clinico-Mycological Study on Suspected Cases of Chromoblastomycosis: Challenges in Diagnosis and Management
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A Clinico-Mycological Study on Suspected Cases of Chromoblastomycosis: Challenges in Diagnosis and Management

机译:染色体成色菌病疑似病例的临床-真菌学研究:诊断和管理中的挑战

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Introduction: Verrucous plaques mimicking chromoblastomycosis are frequently seen in dermatology outpatient departments (OPD). However, no scientific evaluation has been carried out till date from eastern India. So this present endeavour is aimed at a thorough study of those cases to readdress the challenges in diagnosis and management in chromoblastomycosis from this part of the country. Aim: The study is to observe the incidence of proved chromoblastomycosis cases from clinically mimicking conditions and to note therapeutic prospects by use of different antifungal agents. Materials and Methods: Twenty clinically suspected cases attending dermatology OPD were included in this study. Relevant histories were taken. Apart from routine hematological and biochemical investigations, scrapings from lesions were examined by direct microscopy with KOH wet mount, calcoflour white mount and fungal culture. Histopatholgical examination was also done. Any fungal growth was identified by growth characteristics and morphological features. Results: Sclerotic bodies were detected in five samples. Of them three were found to be culture positive. Two growths were identified as Fonsecaea pedrosoi and one as Cladosporium carrionii. Rest 12 cases were diagnosed as either lupus vulgaris (3 cases; 15%), atypical mycobacterial infections (3 cases, 15%), Hypertrophic lichen planus (2, 10%), Hypertrophic DLE plaque (2; 10%), Wart (1, 5%) or fixed cutaneous sporothricosis (1, 5%), zygomycosis (1, 5%). Three cases (15%) were lost in follow up. Cases of chromoblastomycosis were managed with prolonged use of antifungal alone or in combination with saturated solution of potassium iodide and/or debridement. They were followed up for at least six months post treatment. Conclusion: A database comprising diagnostic clues and effective therapeutic intervention have been proposed for these rare subcutaneous mycoses.
机译:简介:皮肤科门诊(OPD)经常出现模仿色母细胞病的疣状斑块。但是,到目前为止,印度东部尚未进行科学评估。因此,本项工作旨在对这些病例进行深入研究,以解决该国该地区色母细胞病的诊断和管理难题。目的:该研究旨在从临床模拟条件下观察已证明的成色菌病病例的发生率,并指出通过使用不同的抗真菌剂的治疗前景。材料和方法:本研究包括20例皮肤科OPD临床可疑病例。记录了相关的历史。除了常规的血液学和生化检查外,还通过直接显微镜检查,用KOH湿法贴壁,白面粉贴壁法和真菌培养法检查病灶刮出物。还进行了组织病理学检查。通过生长特征和形态特征鉴定任何真菌生长。结果:在五个样本中检测到硬化体。他们中的三个被发现对文化具有积极意义。两种生长被鉴定为Fonsecaea pedrosoi,另一种生长为腐霉(Cladosporium carrionii)。其余12例被诊断为寻常性狼疮(3例; 15%),非典型分枝杆菌感染(3例,15%),肥大扁平苔藓(2,10%),肥大性DLE斑块(2; 10%),疣( 1、5%)或固定的皮肤孢子虫病(1、5%),合子菌病(1、5%)。随访中丢失了三例(15%)。长期单独使用抗真菌药或与碘化钾饱和溶液和/或清创术联合使用可治疗成色母细胞增多症。治疗后对其进行至少六个月的随访。结论:已经提出了包含这些罕见皮下真菌病的诊断线索和有效治疗干预措施的数据库。

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