组织胞浆菌病:宫颈淋巴结病的罕见病因。

Q3 Medicine
Mohammad Ahmad Husain, Shyam Chand Chaudhary, Tarun Pal, Shambhavi Sinha, Sunita Kumari, Kamal Kumar Sawlani, Shalini Bhalla
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引用次数: 0

摘要

在过去几年中,世界范围内人类真菌感染的流行率显著上升,主要是由于获得性免疫缺陷综合症(艾滋病)大流行、抗菌剂的广泛使用以及化疗药物治疗肿瘤疾病等因素。组织胞浆菌病是由二形真菌荚膜组织胞浆菌引起的一种机会性真菌感染。它是沿“俄亥俄”和“密西西比”河谷地区的地方性疾病,经常位于被蝙蝠或鸟粪污染的土壤中。在这些流行地区以外发生的病例往往是由于输入性疾病。组织胞浆菌病在印度不被认为是地方病,但据报道,恒河平原地区,特别是西孟加拉邦和北方邦的流行率很高。根据组织浆蛋白皮肤敏感性试验,印度组织浆菌病的患病率为0 - 12.3%。感染通常通过吸入孢子发生,在99%以上的患者中,大多数病例无症状或症状轻微。有症状的病例通常表现为急性肺组织浆菌病,这是一种自限性疾病,类似于非典型肺炎。然而,免疫功能低下的个体,特别是那些t细胞免疫受损的个体,可能无法引起适当的免疫反应,导致播散性组织浆菌病的发展。这种形式的感染可表现为厌食、全血细胞减少、发烧、体重减轻、肝脾肿大以及粘膜溃疡等症状。组织胞浆菌病导致孤立的淋巴结病是不常见的,特别是在印度,肺结核是主要病因在大多数情况下。组织胞浆菌病的症状多样且不明确,常导致误诊或少报感染。因此,必须将组织胞浆菌病列入宫颈淋巴结病的潜在病因清单,特别是在免疫功能低下的个体中。早期医疗干预对防止疾病传播至关重要。组织胞浆菌病合并颈部淋巴结病的表现并不常见,我们在此报告一例。
本文章由计算机程序翻译,如有差异,请以英文原文为准。
Histoplasmosis: A Rare Cause of Cervical Lymphadenopathy.

Over the past few years, there has been a significant rise in the prevalence of human fungal infections worldwide, largely due to factors such as the acquired immunodeficiency syndrome (AIDS) pandemic, widespread use of antibacterial agents, and the utilization of chemotherapeutic agents for treating neoplastic diseases. Histoplasmosis, attributed to the dimorphic fungus Histoplasma capsulatum, is one such opportunistic fungal infection. It is endemic to regions along the "Ohio" and "Mississippi" river valleys and is frequently located in soil tainted by bat or bird feces. Cases occurring outside these endemic areas are often due to imported diseases. Histoplasmosis is not considered endemic in India, but regions with high prevalence have been reported in the Gangetic plain, particularly in West Bengal and Uttar Pradesh. The prevalence of histoplasmosis in India, as determined by histoplasmin skin sensitivity testing, ranges from 0 to 12.3%. Infection typically occurs through inhalation of spores, with the majority of cases being asymptomatic or presenting with minimal symptoms in over 99% of patients. Symptomatic cases usually manifest as acute pulmonary histoplasmosis, which is a self-limiting illness resembling atypical pneumonia. However, immunocompromised individuals, particularly those with impaired T-cell immunity, may fail to elicit appropriate immunological responses, leading to the development of disseminated histoplasmosis. This form of infection can manifest with symptoms such as anorexia, pancytopenia, fever, weight loss, hepatosplenomegaly, as well as mucosal ulceration. Histoplasmosis resulting in isolated lymphadenopathy is uncommon, especially in India, where tuberculosis constitutes the primary etiology in the majority of instances. Diverse and ambiguous symptoms of histoplasmosis often lead to misdiagnosis or underreporting of infections. Thus, it is essential to include histoplasmosis in the list of potential causes for cervical lymphadenopathy, especially among immunocompromised individuals. Early medical intervention is essential to prevent dissemination of the disease. The presentation of histoplasmosis with cervical lymphadenopathy is uncommon, and we present a case of such occurrence here.

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