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免疫功能正常患者的内源性荚膜组织胞浆菌性眼内炎。

Endogenous Histoplasma capsulatum endophthalmitis in an immunocompetent patient.

作者信息

Schlaen Ariel, Ingolotti Mariana, Couto Cristobal, Jacob Nestor, Pineda Gloria, Saravia Mario

机构信息

1 Department of Ophthalmology, Hospital Universitario Austral, Buenos Aires - Argentina.

出版信息

Eur J Ophthalmol. 2015 May 25;25(4):e53-5. doi: 10.5301/ejo.5000550.

DOI:10.5301/ejo.5000550
PMID:25612657
Abstract

PURPOSE

To report on a case of Histoplasma capsulatum endogenous endophthalmitis in an immunocompetent patient.

METHODS

A 30-year-old patient was admitted with floaters and vision impairment of 1 month's duration. He had a history of adrenal insufficiency, together with nasal, septum, and soft palate lesions of 3 months; duration. Culture results from specimens of these lesions were positive for H capsulatum. He was human immunodeficiency virus negative and there was no evidence of immunodepression or history of immunosuppression. Fundus examination revealed multiple fluffy balls with a string of pearls appearance, 2+ vitreous haze, multiple foci of retinochoroiditis inferiorly in the peripheral retina, and a 6-disk area lesion of retinochoroiditis at the superotemporal periphery. Due to poor response to oral itraconazole, a vitrectomy was performed with an intraocular injection of amphotericin B 5 μg/0.1 mL and removal for a vitreous specimen for culture of bacteria and fungi.

RESULTS

Vitreous specimen culture of the yeast at 28°C grew a white filamentous fungus colony, which was again cultured in a brain heart infusion agar medium, where it developed hyaline septate hyphae with microconidia and circular macroconidia with double wall, which was stained with a lactophenol dye at microscopic examination. The macroscopic morphology was consistent with H capsulatum.

CONCLUSIONS

Although endogenous H capsulatum endophthalmitis is a rare entity, it should be considered as a possible etiology even in apparently immunocompetent hosts, especially in patients with history of disseminated disease.

摘要

目的

报告一例免疫功能正常患者发生荚膜组织胞浆菌性内源性眼内炎的病例。

方法

一名30岁患者因出现持续1个月的飞蚊症和视力障碍入院。他有肾上腺功能不全病史,同时伴有持续3个月的鼻腔、鼻中隔和软腭病变。这些病变标本的培养结果显示荚膜组织胞浆菌阳性。他的人类免疫缺陷病毒检测为阴性,且没有免疫抑制的证据或免疫抑制病史。眼底检查发现多个呈珍珠串外观的绒毛球、2+玻璃体混浊、周边视网膜下方多个视网膜脉络膜炎病灶以及颞上周边一个6视盘面积的视网膜脉络膜炎病灶。由于口服伊曲康唑效果不佳,遂进行了玻璃体切除术,并眼内注射5μg/0.1mL两性霉素B,同时取玻璃体标本进行细菌和真菌培养。

结果

玻璃体标本在28°C培养出白色丝状真菌菌落,该菌落再次接种于脑心浸液琼脂培养基中培养,形成透明有隔菌丝、小分生孢子以及具有双层壁的圆形大分生孢子,显微镜检查时用乳酸酚染料进行染色。宏观形态与荚膜组织胞浆菌一致。

结论

尽管内源性荚膜组织胞浆菌性眼内炎是一种罕见疾病,但即使在表面免疫功能正常的宿主中,尤其是有播散性疾病病史的患者,也应将其视为可能的病因。

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