The Importance of Optical Coherence Tomography and Autofluorescence in the Documentation of Papillary Colobomatous Fossette

Thiago Sande Miguel, Vinicius Sande Miguel, Tais Cristina Rossett, Daniel Almeida da Costa, Maurício B Pereira
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Abstract

Aims: To describe the importance of optical coherence tomography and autofluorescence in the documentation of papillary colobomatous fossette. Presentation of Case: F.D.O. A 14-year-old male student is referred for evaluation of the fundus of the eye due to an alteration in the optic disc noticed by another professional who did not feel safe in the follow-up. The patient was completely asymptomatic at the time of the consultation and did not claim previous visual complaints. She denied systemic and ocular comorbidities and did not use any systemic and topical medication. Discussion: The congenital optic disc pit is a rare and typically unilateral congenital anomaly, consisting of a retinal herniation that extends into the subarachnoid space through a lamina cribrosa defect. 8,13,15,16 Although this condition, in most cases, does not present complications and remains asymptomatic, it can sometimes worsen with a significant decrease in visual acuity. This more serious condition can be characterized by important macular alterations, such as serous retinal detachment, cystic degenerations and degenerative pigmentary alterations. 14,16,17,18 The patient in the present report did not have any visual complaints and did not present severe structural and functional retinal damage, which highlights the importance of early diagnosis. Conclusions: The colobomatous papilla pit is characterized by the presence of isolated cavities in the optic disc head secondary to a developmental disorder of the primitive epithelial papilla. Its incidence is 1:10,000 people without sexual or racial predilection. It presents, in most cases, asymptomatic, unilateral in 85-95% of cases and rarely with more than one pit per disc.
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光学相干层析和自体荧光在记录乳头状结肠瘤窝中的重要性
目的:阐述光学相干断层扫描和自身荧光成像在记录乳头状结缔组织中的重要性。病例介绍:F.D.O.一名14岁的男学生因视盘改变而被另一名在随访中感到不安全的专业人员注意到,因此被转介进行眼底评估。患者在咨询时完全无症状,并没有声称以前的视力问题。她否认全身和眼部合并症,没有使用任何全身和局部药物。讨论:先天性视盘凹陷是一种罕见且典型的单侧先天性异常,由视网膜突出组成,通过筛板缺损延伸到蛛网膜下腔。8,13,15,16虽然这种情况在大多数情况下不会出现并发症,也没有症状,但有时会恶化,导致视力明显下降。这种更严重的疾病可以以重要的黄斑改变为特征,如浆液性视网膜脱离、囊性变性和退行性色素改变。14,16,17,18本报告中的患者没有任何视觉主诉,也没有出现严重的结构性和功能性视网膜损伤,这突出了早期诊断的重要性。结论:结缔瘤性乳头窝的特点是视盘头部存在孤立腔,继发于原始上皮乳头的发育障碍。其发病率为1:10 000人,没有性别或种族偏好。在大多数病例中,85-95%的病例表现为无症状,单侧,每个椎间盘很少有超过一个凹陷。
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