Résumé
A 32-year-old male with no known systemic illness presented with unilateral Purtscher-like retinopathy in his left eye 2 weeks after recovering from a severe COVID-19 infection. Fundus examination revealed areas of intraretinal whitening and few cotton wool spots. Multimodal imaging findings were consistent with embolic occlusion of capillaries seen in Purtscher-like retinopathy. The case highlights the effect of virus-directed coagulation cascade activation leading to unilateral microvasculopathy in our patient. The case adds to the spectrum of COVID-19 retinopathy and presses that retina screening strategies should be established for patients suffering from or recovering from severe COVID-19 infection.
Résumé
The coagulation abnormalities and thromboembolic complications of coronavirus 2 (SARS-CoV-2) are now a well-established fact. The hypercoagulable state, the tendency for thromboembolism, and a cytokine surge state have been the exclusive reasons for multiorgan failure and other morbidities that have been regularly reported in COVID-19 patients. Ocular involvement in patients with active disease and those who have recovered is uncommon but not rare. We report a case series of four patients with CRVO, BRVO, CRAO, and vitreous hemorrhage in patients with proven COVID-19 infection and no other systemic ailments. The case series also tries to correlate the elevated D-dimer values, which signify a plausible prothrombotic state with the vaso-occlusive phenomenon in the retina leading to significant visual morbidity.
Résumé
A 6-year old boy presented with mental retardation, hypotonia, abnormal facies, impaired hearing, protuberant eyes, visual impairment, short stature, Axenfeld- Rieger anomaly, a bicuspid aortic valve, and bilateral sensorineural deafness. CT scan of head suggested dysmyelination of the subcortical and periventricular white matter. FISH revealed a subtelomeric microdeletion encompassing both FOXC1 and FOXF2 loci within 6p25. Dysmyelination of the central nervous system has been infrequently described earlier in patients with 6p25 deletion.
Sujets)
Inhibiteurs de l'angiogenèse/usage thérapeutique , Anticorps monoclonaux/usage thérapeutique , Anticorps monoclonaux humanisés , Association thérapeutique , Angiographie fluorescéinique , Humains , Injections , Mâle , Adulte d'âge moyen , Photothérapie dynamique , Rétinopathies/diagnostic , Rétinopathies/traitement médicamenteux , Rétinopathies/physiopathologie , Néovascularisation rétinienne/diagnostic , Néovascularisation rétinienne/traitement médicamenteux , Néovascularisation rétinienne/physiopathologie , Vaisseaux rétiniens/anatomopathologie , Télangiectasie/diagnostic , Télangiectasie/traitement médicamenteux , Tomographie par cohérence optique , Résultat thérapeutique , Facteur de croissance endothéliale vasculaire de type A/antagonistes et inhibiteurs , Acuité visuelle , Corps vitré , Facteur de croissance endothéliale vasculaire de type A/antagonistes et inhibiteurs , Corps vitréSujets)
Sujet âgé , Anticorps monoclonaux/administration et posologie , Néovascularisation choroïdienne/traitement médicamenteux , Femelle , Angiographie fluorescéinique , Études de suivi , Fond de l'oeil , Humains , Injections , Dégénérescence maculaire/complications , Photothérapie dynamique/méthodes , Photosensibilisants/usage thérapeutique , Corps vitréRésumé
A 10-year-old boy, issue of unrelated parents presented with visual impairment, short stature and mental retardation. The presence of a Peters' anomaly, mental retardation, disproportionate short stature, skeletal abnormalities and distinctive facial features (broad forehead, telecanthus, cupid bow shaped upper lip) established the diagnosis of Peters' plus syndrome. Analysis of his genomic DNA revealed a homozygous deletion in the beta1,3-galactosyltransferase-like gene (B3GALTL), a recently identified gene.
Sujets)
Malformations multiples/génétique , Enfant , Galactosyltransferases/génétique , Délétion de gène , Humains , Inde , Mâle , Déficience intellectuelle/génétique , Mutation/génétique , SyndromeRésumé
Holi festival is celebrated in India traditionally by applying colors on one another. Various ocular adverse effects of these colors have been reported including conjunctivitis and corneal abrasion. We report a case of bilateral periorbital necrotizing fasciitis, following exposure to Holi colors. General physicians might encounter more such cases after exposure to Holi colors. In India, these colors are prepared on a small scale and lack any quality checks. Use of such toxic colors should be discouraged, and all doctors should caution people against using synthetic dyes. This case report highlights the need to put manufacturing of Holi colors under guidelines of the Food and Drug Cosmetic Act and the Bureau of Indian Standards.
Sujets)
Administration par voie topique , Agents colorants/administration et posologie , Diagnostic différentiel , Fasciite nécrosante/induit chimiquement , Humains , Mâle , Adulte d'âge moyen , Maladies de l'orbite/induit chimiquementRésumé
We report two siblings with the rare entity of familial calcific band-shaped keratopathy (BSK). Detailed ophthalmic and systemic investigations failed to reveal any underlying causative pathology. Topical disodium ethylenediamine-tetraacetate (EDTA) was applied for 30 min to all four eyes. In addition the right eye of the younger sibling required a superficial keratectomy. An improvement in corneal clarity was seen in the immediate postoperative period in both siblings. Histopathology of the keratectomy specimen revealed linear extracellular sub-epithelial granular calcium deposits. However, an early recurrence was noted in all four eyes at four weeks postoperatively. We report the second instance in the English literature of this entity. Band-shaped keratopathy presenting without an obvious etiology merits a complete systemic and ophthalmic workup. Patients with familial idiopathic BSK could be cases with poor prognosis for treatment with EDTA due to an early recurrence of the disease.