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组织胞浆菌病——一种强大的入侵者,即使在免疫功能正常的患者中也是如此。

Histoplasmosis-a great invader, even in immunocompetent patient.

作者信息

Banik Sudip Kumar, Tofail Tania, Arefin Muhammad Sayedul, Arafat Shohael Mahmud

机构信息

Department of Internal Medicine, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

Department of Endocrinology, Bangabandhu Sheikh Mujib Medical University, Dhaka, Bangladesh.

出版信息

Radiol Case Rep. 2025 Jan 24;20(4):1979-1982. doi: 10.1016/j.radcr.2024.12.056. eCollection 2025 Apr.

Abstract

Disseminated histoplasmosis (DH) is a rare deep fungal infection caused by Histoplasma capsulatum and it usually occurs in immunocompromised patients like in acquired immunodeficiency syndrome (AIDS) or patients getting any immunosuppressive therapy. Histoplasmosis usually remains unrecognized in immunocompetent individuals. Here we are reporting a case of a 55-year-old immunocompetent man with DH who presented to us with dysphagia, occasional vomiting, slurred speech with left sided hemipaeresis, weight loss and after hospital admission he developed fever, but no cough. On investigations, he was found to have bilateral adrenal mass, rim enhancing lesion in the brain, nodular lesions in duodenum and soft tissue mass in lung. DH was confirmed by the presence of Histoplasma capsulatum in the cytopathology of adrenal mass and histopathology of tissue from duodenum which revealed PAS positive yeasts. He was treated with itraconazole rather than recommended choice of liposomal amphotericin B as he could not afford this expensive drug. After getting itraconazole on subsequent follow up at 4 months, he was found to be clinically improving, gained weight about 10 kg with disappearance of other symptoms. DH may present with atypical symptoms like dysphagia, slurred speech with hemiparesis rather than common presentation with fever, cough or weight loss. Though DH is more common in immunocompromised patients, if multisystem involvement occurs in immunocompetent patients, we should always consider deep fungal infection as one of the differentials.

摘要

播散性组织胞浆菌病(DH)是一种由荚膜组织胞浆菌引起的罕见深部真菌感染,通常发生在免疫功能低下的患者中,如获得性免疫缺陷综合征(AIDS)患者或接受任何免疫抑制治疗的患者。组织胞浆菌病在免疫功能正常的个体中通常未被识别。在此,我们报告一例55岁免疫功能正常的男性患有DH,他因吞咽困难、偶尔呕吐、言语不清伴左侧偏瘫、体重减轻前来就诊,入院后出现发热,但无咳嗽。经检查,发现他双侧肾上腺有肿块,脑部有边缘强化病灶,十二指肠有结节性病灶,肺部有软组织肿块。通过肾上腺肿块细胞病理学检查及十二指肠组织病理学检查发现荚膜组织胞浆菌,证实为DH,十二指肠组织病理学检查显示PAS阳性酵母。由于他负担不起昂贵的脂质体两性霉素B,因此接受了伊曲康唑治疗,而不是推荐的治疗药物。在接受伊曲康唑治疗4个月后的后续随访中,发现他临床症状改善,体重增加约10kg,其他症状消失。DH可能表现为吞咽困难、言语不清伴偏瘫等非典型症状,而不是常见的发热、咳嗽或体重减轻症状。虽然DH在免疫功能低下的患者中更常见,但如果免疫功能正常的患者出现多系统受累,我们应始终将深部真菌感染列为鉴别诊断之一。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/6ea2/11804264/f63b0a505fa7/gr1.jpg

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