Leber’s congenital amaurosis (LCA) is a known inherited retinal disease (IRD) associated with severe visual loss, nystagmus, amaurotic pupils, oculo-digital sign and markedly reduced or absent electroretinograms (ERG). Retinal astrocytic hamartomas (RAH) is a benign vascularized glial tumor of the retina. There is no known association of these two entities, more so in siblings.
Case presentation
A pair of siblings diagnosed as LCA who presented with RAH with no extraocular symptoms or signs of phakomatosis were imaged. Multimodal imaging was performed and are elaborately described in this article.
Conclusion
LCA in siblings with multiple RAHs is an extremely rare association. Recent advances in retinal imaging tools have aided in diagnosing even subtle and early RAH with high sensitivity using Infrared imaging (IRI) and Optical coherence tomography (OCT).
Hinweise
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Abkürzungen
LCA
Lebers Congenital Amaurosis
IRD
Inherited retinal disorder
ERG
Electroretinograms
RAH
Retinal astrocytic hamartoma
BCVA
Best corrected visual acuity
RPE
Retinal pigment epithelium
SD-OCT
Spectral domain – Optical coherence tomography
NFL
Nerve fiber layer
IRI
Infra-red imaging
OCT-A
Optical coherence tomography- angiography
Background
Lebers Congenital Amaurosis (LCA) is an inherited retinal disorder (IRD) which is characterized by severe visual loss which maybe present congenitally or in early infancy. It is associated with nystagmus, amaurotic pupils, oculo-digital sign and markedly reduced or absent electroretinograms (ERG) [1]. We report two siblings with non-syndromic forms of LCA with multiple retinal astrocytic hamartomas (RAHs) in the eyes. We describe the findings of multimodal imaging techniques in these eyes in the present case report.
Case presentation
An 8 years old boy presented with complaint of painless visual deterioration in both eyes (BE) since early childhood. On examination, the best corrected visual acuity (BCVA) in the right eye (RE) was 6/18, N18 and in the left eye (LE) was counting finger at 10 cm, N60 with nystagmus in BE. Supero-nasal subluxation of the lens was present in BE. Applanation tonometry was normal in BE. Fundus examination of BE showed normal optic disc with generalized attenuation of vessels with retinal pigment epithelium (RPE) atrophy and pigmentary alterations in the retina. A reddish-orange hue was seen at the fovea and atrophic maculopathy was noted. There were characteristic multiple off -white relatively well defined lesions, which were more marked along the arcades in the RE with a single lesion located on the inferonasal retinal quadrant in the fellow eye (Fig. 1).
Fig. 1
Colored fundus picture of RE and LE showing generalized vascular attenuation, RPE alterations and multiple RAH. a SD-OCT of RE through fovea showing altered IS-OS junction. b SD-OCT of RE through the lesion showing hyper-reflective lesion in nerve fiber layer with posterior shadowing without any calcifications. c- SD-OCT of LE through fovea showing altered IS-OS junction. d SD-OCT of LE through the lesion showing hyper-reflective lesion in nerve fiber layer with posterior shadowing without any calcifications
×
Anzeige
Spectral domain optical coherence tomography (SD-OCT) depicted sub-foveal thinning with RPE atrophy in the RE (Fig. 1a). Scans passing just over the lesion revealed a hyperreflective dome shaped mass within the nerve fiber layer (NFL) along with a posterior optical shadowing associated with the disorganization of inner retinal layers (Fig. 1b). SD-OCT scans of the fellow eye revealed similar features in the LE (Fig. 1c and d).
SS-OCT (Swept-Source Optical Coherence tomography) through the fovea of RE showed an opaque lesion arising in the NFL with a smooth transition from retina and posterior shadowing. All other retinal layers appeared compressed along with mild thinning of choroid beneath the tumorous lesion (Fig. 2a). However, SS-OCT of LE could not be performed due to nystagmus and poor fixation. OCT-A over the retinal tumor showed a feeder vessel with an abnormal network of capillary plexus emanating from it (Fig. 2b). Autofluorescence (AF) was inconclusive in BE. Infra-red imaging (IRI) showed numerous hypo reflectance lesions in BE corresponding to RAH at the posterior pole (Fig. 2c). ERG showed markedly extinguished responses with both photopic and scotopic stimuli (Fig. 3).
Fig. 2
a SS-OCT of RE showing thinned out retina and choroid. b OCT-A of RE through the lesion showing abnormal capillary network. c- IRI of RE and LE showing multiple hypo-reflectance lesions
Fig. 3
ERG showing grossly diminished photopic and scotopic response
×
×
Systemic evaluation by a pediatrician revealed no signs of Tuberous sclerosis or any associated syndrome. There were no systemic features of renal or hepatic dysfunction, neurological deficit, phacomatoses or deafness. MRI (Magnetic resonance imaging) cranium and abdominal ultrasound was normal along with normal renal functions. Gene mapping could not be performed due to limited financial resources.
His pedigree charting revealed a high refractive error in his sister. She was also assessed for any associated syndromes. She was 11 years old, and her BCVA was 6/9, N6 with normal slit-lamp biomicroscopic findings in both eyes. Fundus evaluation revealed some pigmentary alteration in BE with normal macula (Fig. 4). An isolated retinal hamartoma was noted in far periphery in the RE.
Fig. 4
Colored fundus picture of RE and LE of the elder sister showing generalized vascular attenuation and RPE alterations
×
Anzeige
Based on the above clinical findings of severe visual loss, nystagmus, hyperopia, amaurotic pupils, abnormally pigmented fundi and macular atrophy and with detailed systemic investigations, a diagnosis of presumed non- syndromic LCA with RAH was made. Since multiple alleles have been associated with LCA, gene therapy is highly costly [2] and since RAHs are known to have a benign natural course [2], we preferred to observe them with a follow-up every 6 months.
Discussion and conclusion
The prevalence of LCA is between 1 in 33,000 to 1 in 81,000 and accounts for ≥5% of all IRD [3, 4]. It is characterized by severely impaired vision from birth or first few months of life, and often accompanied by nystagmus and poor pupillary light responses The retina may be normal looking or develop abnormalities like disc pallor, vascular attenuation, mild peripheral pigmentary retinopathy or atrophic maculopathy [1]. The affected infants usually have high hyperopia with severely affected or undetectable ERG [1]. RAH is a benign vascularized glial tumor of the retina which could be acquired or congenital, wherein congenital RAH are more common and strongly associated with tuberous sclerosis complex.
Ambiya et al. [5] reported an optic nerve head hamartoma with LCA. However, to the best of our knowledge and the literature available, we report the first case of two siblings with non-syndromic LCA with RAHs. The male child showed multiple hamartoma scattered throughout the fundus with poor visual acuity, while his elder sister showed a single retinal hamartoma in far periphery in the right eye and maintained a good vision in both eyes.
Recently, studies on RAHs have highlighted the role of IRI and SD-OCT in detecting subtle changes which were otherwise not visible on clinical examination or colored fundus photography or AF [6, 7] which make them indispensable tool in detecting subtle or small tumors and following up these eyes. IRI in our patient reflected > 14 and 9 hamartomas in RE and LE while RFI could highlight only 7 and 2 in RE and LE respectively. We postulate that IRI could be used to monitor the other sibling for development of any acquired hamartomas in the future. The usability and repeatability of SS-OCT and OCT-A are identical to the description in the available literature [8, 9].
In conclusion, we describe siblings with clinical and ERG findings suggestive of LCA associated with RAHs. The RAHs appear as hyper-reflective dome shaped lesions at the level of NFL and reveal a feeder vessel on the OCT-A scans. We furthermore highlight the role of IRI in detecting subtle changes which are otherwise not detectable on fundus examination and monitoring these patients.
Acknowledgements
None.
Ethics approval and consent to participate
Consent to participate was obtained from the parents in a written manner.
Consent for publication
Written informed consent was obtained from the patient’s parent for publication of this Case report and any accompanying images. A copy of the written consent is available for review by the Editor of this journal.
Anzeige
Competing interests
None.
Open AccessThis article is licensed under a Creative Commons Attribution 4.0 International License, which permits use, sharing, adaptation, distribution and reproduction in any medium or format, as long as you give appropriate credit to the original author(s) and the source, provide a link to the Creative Commons licence, and indicate if changes were made. The images or other third party material in this article are included in the article's Creative Commons licence, unless indicated otherwise in a credit line to the material. If material is not included in the article's Creative Commons licence and your intended use is not permitted by statutory regulation or exceeds the permitted use, you will need to obtain permission directly from the copyright holder. To view a copy of this licence, visit http://creativecommons.org/licenses/by/4.0/. The Creative Commons Public Domain Dedication waiver (http://creativecommons.org/publicdomain/zero/1.0/) applies to the data made available in this article, unless otherwise stated in a credit line to the data.
Publisher’s Note
Springer Nature remains neutral with regard to jurisdictional claims in published maps and institutional affiliations.
Die Verwendung von Ophthalmika in der Schwangerschaft und Stillzeit stellt immer eine Off-label-Anwendung dar. Ein Einsatz von Arzneimitteln muss daher besonders sorgfältig auf sein Risiko-Nutzen-Verhältnis bewertet werden. In der vorliegenden …
Die endogene Endophthalmitis ist eine hämatogen fortgeleitete, bakterielle oder fungale Infektion, die über choroidale oder retinale Gefäße in den Augapfel eingeschwemmt wird [ 1 – 3 ]. Von dort infiltrieren die Keime in die Netzhaut, den …
Eine endogene Endophthalmitis stellt einen ophthalmologischen Notfall dar, der umgehender Diagnostik und Therapie bedarf. Es sollte mit geeigneten Methoden, wie beispielsweise dem Freiburger Endophthalmitis-Set, ein Keimnachweis erfolgen. Bei der …
Die bestmögliche Wundheilung der Kornea, insbesondere ohne die Ausbildung von lichtstreuenden Narben, ist oberstes Gebot, um einer dauerhaften Schädigung der Hornhaut frühzeitig entgegenzuwirken und die Funktion des Auges zu erhalten.
Update Augenheilkunde
Bestellen Sie unseren Fach-Newsletterund bleiben Sie gut informiert.
