Optic Chiasmal Fungal Granuloma - Rare Cause of Blindness

Saket Saurabh, Nimesh Jain, Hrushikesh Kharosekar, Vernon Velho
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Abstract

Intracranial fungal infections are rare. Their presentation is mostly subtle, clinically atypical in presentation, and they are usually mistaken for tuberculosis or brain tumour. Aspergillosis is the most common cause of intracranial fungal infections. Fungal infection enters the brain directly from the paranasal sinuses, ear, skull bone, or haematogenous spread from the lungs and gastrointestinal tract, or direct inoculation during surgery or trauma. The pathology depends on the route of spread, host immunity, and type of fungus. Intracranially, fungal infection invades brain matter or blood vessels. [1] The rarity of brain fungal infection, with nonspecific clinical picture, and progression to a fatal outcome provides considerable challenges for both diagnosis and management. Invasive sino-orbital fungal infections are rarely reported in immunocompetent patients in literature.  We could not find anything related to primary fungal granuloma of the optic tract reported in literature. We report a case of primary fungal granuloma of optic chiasm in an immunocompetent patient.[2] 13-year-old female patient presented to us with sudden onset of loss of vision in both eyes. There were no other complaints. On neurological examination, there was no vision in both eyes (no perception of light). On fundoscopy, there was bilateral optic atrophy. Rest of the neurological examination was normal. Patient was investigated for magnetic resonance imaging (MRI) of brain with contrast study. MRI of brain was suggestive of a 2.2 x 1.8 x 1.6 cm mass in suprasellar region with its epicentre in the optic chiasma and extending to both optic nerves and optic tract. The lesion was separate from the underlying pituitary gland. The lesion was iso-intense on T1 weighted images and hyper-intense on T2 weighted images. It showed homogenous post-contrast enhancement. Our primary differential diagnosis was optic nerve glioma. Patient underwent immediate surgery, right peritoneal craniotomy, for excision of lesion. Intra-operatively, a firm yellowish white colored lesion arising from the optic chiasm was seen. Safe subtotal excision was done. Post-operative, there was no improvement in vision.
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视交叉真菌性肉芽肿——罕见的致盲原因
颅内真菌感染是罕见的。它们的表现大多很微妙,临床上不典型,通常被误认为是肺结核或脑瘤。Aspergillosis是颅内真菌感染最常见的原因。真菌感染直接从鼻窦、耳朵、颅骨进入大脑,或从肺部和胃肠道血液传播,或在手术或创伤期间直接接种。病理学取决于传播途径、宿主免疫力和真菌类型。在颅内,真菌感染会侵入大脑或血管。[1] 脑真菌感染的罕见性,非特异性的临床表现,以及进展到致命的结果,为诊断和治疗提供了相当大的挑战。文献中很少报道免疫活性患者的侵袭性眶内真菌感染。我们没有发现任何与文献中报道的原发性视路真菌肉芽肿有关的内容。我们报告了一例免疫功能正常患者的视交叉原发性真菌肉芽肿。[2] 一位13岁的女性患者突然出现双眼失明。没有其他抱怨。在神经系统检查中,两只眼睛都没有视力(没有光感)。眼底镜检查发现双侧视神经萎缩。其余神经系统检查正常。对患者进行脑部磁共振成像(MRI)对比研究。大脑MRI提示鞍上区有2.2 x 1.8 x 1.6 cm的肿块,其中心位于视交叉,并延伸至视神经和视束。病变与下方的垂体分离。病变在T1加权图像上是等强度的,而在T2加权图像上则是超强度的。它显示出均匀的对比度增强。我们的主要鉴别诊断是视神经胶质瘤。患者立即接受了右腹膜开颅手术,切除病变。术中可见视交叉引起的黄白色病变。进行了安全的次全切除术。术后视力没有改善。
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