Histoplasmosis of Adrenal Gland: A 5 Years' Review from a Multispecialty Diagnostic Centre.

IF 0.9 Q3 MEDICINE, GENERAL & INTERNAL Journal of Laboratory Physicians Pub Date : 2023-06-01 DOI:10.1055/s-0042-1757587
Kumkum Bhattacharyya, Suranjan Pal, Ashis Dutta, Pinak Pani Bhattachryya, Saurabh Laskar
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Abstract

Objective  Histoplasmosis is an infectious disease caused by the dimorphic fungus Histoplasma capsulatum . Histoplasmosis is considered to be endemic to India, especially the Gangetic belt. Disseminated histoplasmosis may affect almost all systems. Disseminated histoplasmosis with asymptomatic adrenal involvement has been described in immunocompromised patients, whereas isolated adrenal involvement as the presenting manifestation in immunocompetent is uncommon. We aimed to determine the clinicopathological and radiological findings of adrenal histoplasmosis in immunocompetent patients attending a multispecialty diagnostic center referred from different clinics and hospitals. Materials and Methods  All tissue samples were initially examined microscopically by performing potassium hydroxide (KOH) wet mounts, followed by culture on two tubes of Sabouraud dextrose agar and phase conversion. Histopathological correlation was done using tissue stains, hematoxylin and eosin, periodic acid-Schiff, and Gomori methenamine silver. Results  We evaluated 84 clinically suspected cases radiologically for adrenal mass. The pathological and microbiological work-up was done from these suspected cases. A total of 19 cases were evident from the tissue stain and fungal culture methods. The affected population were mostly above 45 years and male. Seven patients had bilateral adrenal involvement. All these patients received amphotericin B and/or itraconazole treatment, which led to symptomatic improvement in most cases. Conclusion  Diagnosis of invasive fungal infection requires a high index of suspicion, especially in immunocompetent patients presenting with nonspecific symptoms, clinical signs, and laboratory and radiological features that often resemble adrenal neoplasms. Clinical specimens, together with fungal culture, must be sent for cytopathology/histopathology for a definite diagnosis and appropriate management.

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肾上腺组织胞浆菌病:一个多专业诊断中心的5年回顾。
目的组织胞浆菌病是一种由双形真菌荚膜组织胞浆菌引起的传染病。组织胞浆菌病被认为是印度特有的,特别是恒河带。弥散性组织胞浆菌病可影响几乎所有系统。无症状肾上腺受累的弥散性组织胞浆菌病在免疫功能低下患者中有报道,而孤立的肾上腺受累作为免疫功能正常患者的表现并不常见。我们的目的是确定来自不同诊所和医院的多专科诊断中心的免疫功能正常患者的肾上腺组织浆菌病的临床病理和放射学表现。材料和方法所有组织样品首先通过氢氧化钾湿载显微镜检查,然后在两管Sabouraud葡萄糖琼脂上培养并进行相转化。采用组织染色、苏木精和伊红、周期性酸-希夫和Gomori甲基苯丙胺银进行组织病理学相关性分析。结果对84例临床疑似肾上腺肿块进行影像学评价。对这些疑似病例进行了病理和微生物检查。组织染色和真菌培养共检出19例。感染人群以45岁以上男性居多。7例患者双侧肾上腺受累。所有患者均接受两性霉素B和/或伊曲康唑治疗,大多数患者的症状得到改善。结论侵袭性真菌感染的诊断需要高度的怀疑,特别是在免疫功能正常的患者,其症状、临床体征、实验室和放射学特征往往与肾上腺肿瘤相似。临床标本,连同真菌培养,必须送去细胞病理学/组织病理学明确诊断和适当的管理。
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来源期刊
Journal of Laboratory Physicians
Journal of Laboratory Physicians MEDICINE, GENERAL & INTERNAL-
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99
审稿时长
31 weeks
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