A Case Report on Laryngeal histoplasmosis masquerading as Tuberculosis

Naznin Naher
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Abstract

Immunocompromised patients typically develop laryngeal histoplasmosis as a result of the fungus spreading from the lungs to other organs. Primary isolated laryngeal histoplasmosis is uncommon. We reported a unique case of laryngeal histoplasmosis in a 25-year-old male who initially had a preliminary diagnosis of tuberculosis. A 25-year-old man complained of dysphagia and increasing hoarseness of voice for three months when he first came into the medical department. He has also had a cough and intermittent fever for 1 month. Bilateral post-TB fibrosis with bronchiectasis, a consequence of pulmonary tuberculosis infection, was the patient’s previous diagnosis. In addition to that, he is also receiving treatment for his chronic calcific pancreatitis with pancreatic enzyme supplements and dietary modifications. During physical examination, the patient showed mild anemia, no cervical lymphadenopathy or thyromegaly, and bronchiectasis features identified by lung auscultation findings. We thus reached a working diagnosis of disseminated tuberculosis including the larynx and lungs. The results of the blood profile showed normocytic normochromic anemia, low Hb, and high ESR. Fungal stain, gene X-pert for MTB/PCR, and microscopic analysis of the sputum were all normal, and the sputum C/S was consistent with the growth of normal flora. Vocal cords were normal, and fiber optic laryngoscopy revealed a swollen arytenoid region and granulo-nodularity in the posterior larynx. Under gross examination, the biopsy sample was found to consist of irregular grayish-white soft tissue fragments. Histology revealed granulation tissue, which was heavily infiltrated with acute and chronic inflammatory cells, as well as a small number of multinucleated giant cells. Furthermore, we used GMS and Pas staining to look for fungus, and the results showed round to oval yeast that was consistent with histoplasmosis. The fungus Histoplasmacapsulatum, which is a dimorphic fungus causes histoplasmosis, one of the most common causes of chronic granulomatous diseases.In North America, histoplasmosis is the most prevalent type of endemic mycosis. A portion of Africa, Australia, and Eastern Asia, especially India and Malaysia, are among the other endemic areas. Pharyngeal and laryngeal infections caused by Histoplasmacapsulatum are an uncommon manifestation that usually refers to the mucocutaneous type of chronic disseminated dissemination. The first signs and symptoms typically include fatigue malaise, loss of weight, hoarseness of voice, dysphagia, and odynophagia. Being a rare occurrence, laryngeal histoplasmosis is frequently misdiagnosed, which can have disastrous consequences for the patient. Diagnosis difficulties are probably one of the explanations for the small number of documented cases. When a patient exhibits symptoms of granulomatous inflammation or laryngeal masses, the physician should be aware of the possibility of laryngeal histoplasmosis and take it into consideration when making a differential diagnosis. Bangladesh J Medicine 2024; Vol. 35, No. 2, Supplementation: 173-174
伪装成肺结核的喉组织胞浆菌病病例报告
免疫力低下的患者通常会因真菌从肺部扩散到其他器官而患上喉组织胞浆菌病。原发性孤立的喉组织胞浆菌病并不常见。我们报告了一例独特的喉组织胞浆菌病病例,患者为一名 25 岁男性,最初初步诊断为肺结核。一名 25 岁的男子刚到医疗部门就诊时,主诉吞咽困难和声音越来越嘶哑,已经持续了三个月。他还出现咳嗽和间歇性发热 1 个月。患者之前的诊断是肺结核感染导致的双侧肺结核后纤维化伴支气管扩张。此外,他还在接受胰酶补充剂和饮食调整治疗慢性钙化性胰腺炎。体格检查时,患者表现为轻度贫血,无颈部淋巴结肿大或甲状腺肿大,肺部听诊发现支气管扩张特征。因此,我们得出了包括喉部和肺部在内的播散性肺结核的诊断结果。血常规结果显示,患者为正常红细胞性贫血,低 Hb,高 ESR。真菌染色、MTB/PCR 基因 X-pert 和痰液显微镜分析均正常,痰液 C/S 与正常菌群生长一致。声带正常,光纤喉镜检查发现杓状区肿胀,喉后部有颗粒状结节。大体检查发现,活检样本由不规则的灰白色软组织碎片组成。组织学检查显示,肉芽组织被大量急性和慢性炎症细胞以及少量多核巨细胞浸润。此外,我们还使用了 GMS 和 Pas 染色法来寻找真菌,结果显示出圆形至椭圆形的酵母菌,与组织胞浆菌病一致。组织胞浆菌是一种二形真菌,它引起的组织胞浆菌病是慢性肉芽肿病最常见的病因之一。非洲部分地区、澳大利亚和东亚,尤其是印度和马来西亚,也是组织胞浆菌病的流行地区。由组织胞浆菌引起的咽部和喉部感染是一种不常见的表现,通常是指粘膜型慢性播散性传播。最初的症状和体征通常包括疲劳乏力、体重减轻、声音嘶哑、吞咽困难和吞咽异物。喉组织胞浆菌病是一种罕见病,经常被误诊,这可能会给患者带来灾难性后果。诊断困难可能是记录病例较少的原因之一。当患者出现肉芽肿性炎症或喉部肿块症状时,医生应意识到喉组织胞浆菌病的可能性,并在进行鉴别诊断时将其考虑在内:173-174
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