儿科基底球菌根症:一种不常见且被误诊的实体
Ritul Choudhary1, Charu Tiwari2, Nitinkumar Borkar2
1Department of Dermatology, AIIMS, Raipur, Chhattisgarh, India.
Indian dermatology online journal
|October 3, 2024
概括
贝西迪奥博洛米科斯是一种罕见的真菌感染,在幼儿中经常被误诊,需要高度怀疑才能及时诊断. 抗真菌疗法,特别是三醇,在治疗这种皮下紫外线病时表现出良好的疗效和安全性.
科学领域:
- 菌类学 菌类学是指菌类学.
- 儿科手术 儿科手术
- 传染性疾病 传染性疾病
背景情况:
- 贝西迪奥博洛米科斯是一种罕见的,慢性皮下结核病,主要影响热带地区.
- 它的稀有性往往导致误诊,延迟适当的治疗.
- 这项研究侧重于在印度的第三级护理中心管理的儿科病例.
研究的目的:
- 审查幼儿基础骨质菌根病的临床表现,诊断和管理.
- 为了突出诊断这种罕见的真菌感染的挑战.
- 评估抗真菌治疗在儿科患者中的有效性和安全性.
主要方法:
- 一项对6名被诊断患有巴西迪奥博洛米科斯的儿科患者的回顾性审查.
- 收集的数据包括患者人口统计,临床表现,诊断方法,治疗和结果.
- 患者在2018年1月至2022年6月期间在印度中部的一个高等院校进行了治疗.
主要成果:
- 所有6名患者都是5岁以下的男性,没有并发病症 (免疫竞争).
- 所有病例最初都在外部医院被误诊.
- 通过活检及时诊断和用三醇抗真菌药物的有效管理导致了具有最小副作用的良好结果.
结论:
- 儿童的基底球菌根症虽然很少见,但需要高度的怀疑指数才能确诊.
- 活检对于确定诊断至关重要.
- 三醇抗真菌药物为儿科基底博菌症提供了安全有效的治疗选择.
更多相关视频
10:04Analysis of 18FDG PET/CT Imaging as a Tool for Studying Mycobacterium tuberculosis Infection and Treatment in Non-human Primates
Published on: September 5, 2017
18.8K
06:49Reduced Itraconazole Concentration and Durations Are Successful in Treating Batrachochytrium dendrobatidis Infection in Amphibians
Published on: March 14, 2014
11.6K
相关概念视频
Pedigree Analysis
84.1K
Overview
84.1K
Pulmonary Tuberculosis IV
134
Tuberculosis, more commonly referred to as TB, is an infectious disease stemming from Mycobacterium tuberculosis. While it primarily impacts the lungs, TB can also affect other body areas. Given its severity and global impact, timely and accurate diagnosis is crucial for controlling its spread and improving patient outcomes.
Several diagnostic approaches are used to detect TB. The conventional method is the Tuberculin Skin Test (TST), also known as the Mantoux test. However, this method has...
Several diagnostic approaches are used to detect TB. The conventional method is the Tuberculin Skin Test (TST), also known as the Mantoux test. However, this method has...
134
Pulmonary Tuberculosis III
312
Tuberculosis (TB) is a contagious infection primarily affecting the lung parenchyma but which can also affect other body parts. TB can be classified based on disease development, presentation, and the affected anatomical site.
The first classification is based on the development of the disease, and it includes the following categories:
The first classification is based on the development of the disease, and it includes the following categories:
312
Pulmonary Tuberculosis II
213
Tuberculosis, or TB, is a bacterial infectious disease caused by Mycobacterium tuberculosis. While its primary impact is on the lungs, leading to pulmonary tuberculosis, it can also affect various other organs, a condition referred to as extrapulmonary tuberculosis.
Here is a detailed explanation of its pathophysiology:
Transmission: The process begins when a person inhales droplet nuclei containing M. tuberculosis. These are typically released into the air when an individual with pulmonary or...
Here is a detailed explanation of its pathophysiology:
Transmission: The process begins when a person inhales droplet nuclei containing M. tuberculosis. These are typically released into the air when an individual with pulmonary or...
213
Pulmonary Tuberculosis I
221
Tuberculosis, often called TB, is a contagious illness primarily caused by Mycobacterium tuberculosis. It mainly affects the lung parenchyma but can also impact other body parts.
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
Causative Organism
The primary infectious agent causing tuberculosis is Mycobacterium tuberculosis, a slow-growing, acid-fast, aerobic rod that exhibits sensitivity to heat and ultraviolet light. Instances of Mycobacterium bovis and Mycobacterium avium contributing to the development of TB infection are rare.
Mode of...
221
Inborn Errors of Metabolism
142
Phenylketonuria (PKU) is a protein metabolism disorder characterized by high blood levels of the amino acid phenylalanine. This results from a mutation in the gene responsible for phenylalanine hydroxylase, an enzyme that converts phenylalanine into tyrosine. When this enzyme is deficient, phenylalanine builds up in the blood, leading to symptoms such as vomiting, rashes, seizures, growth deficiency, and severe mental retardation. An early diagnosis and a diet restricting phenylalanine intake...
142
