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1.
Medicina (Kaunas) ; 59(2)2023 Feb 20.
Article in English | MEDLINE | ID: mdl-36837613

ABSTRACT

Digital device usage has increased significantly in last decade among all age groups, both for educational and recreational purposes. Computer vision syndrome (CVS), also known as digital eye strain (DES), represents a range of ocular, musculoskeletal, and behavioral conditions caused by prolonged use of devices with digital screens. This paper reviews the principal environmental, ocular, and musculoskeletal causes for this condition. Due to the high prevalence of DES and frequent usage of digital devices, it is important that eye care practitioners be able to provide advice and management options based on quality research evidence.


Subject(s)
Asthenopia , Humans , Asthenopia/epidemiology , Asthenopia/etiology , Computers , Syndrome , Risk Factors , Prevalence
2.
Rom J Ophthalmol ; 66(2): 112-117, 2022.
Article in English | MEDLINE | ID: mdl-35935080

ABSTRACT

Objective: The purpose of this study was to assess the quality of vision of patients who have chosen orthokeratology, and to identify different incidents that occur in patients who used this type of therapy. Materials and methods: The study was conducted on a group of 10 patients who had a follow-up period of at least 4 years and presented regularly to ophthalmological check-ups. The clinical parameters that were analyzed are the following: ocular refraction before and after orthokeratology therapy, the appearance of corneal topography, the slit-lamp examination of the anterior segment of the eye, incidents determined by night contact lenses, as well as ocular comfort. Results: Issues produced by night lenses occurred in two cases due to deficient hygiene and care and in one case due to disruption of lens wear. Menicon lenses were used in 7 cases and Precilens lenses were used in 3 cases. The initial visual acuity without correction was between 0.02 and 0.7, and after orthokeratology 8 out of 10 patients had a visual acuity of 1. Conclusions: In our study, orthokeratology therapy demonstrated its efficiency in slowing myopia progression and no severe complication was observed during the follow-up period.


Subject(s)
Contact Lenses , Myopia , Cornea , Corneal Topography , Humans , Myopia/diagnosis , Myopia/therapy , Refraction, Ocular , Visual Acuity
3.
Rom J Morphol Embryol ; 62(4): 907-915, 2021.
Article in English | MEDLINE | ID: mdl-35673810

ABSTRACT

BACKGROUND: Conjunctival pigmented neoplasia can be benign, premalignant or malignant tumors. Our study aims to establish the epidemiological, gross morphological and immunohistopathological features of the conjunctival pigmented lesions in pediatric and adolescent patients (<18 years), to establish an accurate diagnosis. PATIENTS, MATERIAL AND METHODS: This is a retrospective case series study conducted within two Ophthalmology Clinics from Iasi, Romania, on seven pediatric and adolescent patients. Using the Clinical Observation Chart and the Pathology Registers over a six-years period (January 2015-December 2021), we noted the patients' demographic data, clinical data, and ophthalmological investigations of the lesion, as well as the type of their treatment. All histological sections stained with Hematoxylin-Eosin (HE) and with five antibodies [pan-cytokeratin (pan-CK) AE1∕AE3, S100 protein, Melan A, human melanoma black 45 (HMB45), and Ki67] were re-examined by four pathologists for each case, to identify the type of the conjunctival lesion and its histological and immunohistochemical features. RESULTS: The mean age of all patients was 10.28 years, and the female∕male ratio was 1.3. Right eye was more often affected (71.42%). 71.42% of cases presented an elevated lesion, 57.14% of cases showed a lightly pigmented lesion, but 14.28% of cases exhibited a pink lesion and this feature described the inflamed juvenile conjunctival nevus. In all cases (100%) the conjunctival pigmented tumor was removed with safety margins. The microscopic examination revealed a compound melanocytic nevus in 57.14% cases, a junctional conjunctival nevus in 14.28% cases, an inflamed juvenile nevus in 14.28% cases, and a conjunctival melanoma arising from a pre-existing nevus in 14.28% cases. In all cases of nevi, the nevoid melanocytes showed strong immunopositivity for Melan A and S100 protein, variable and weak immunopositivity for HMB45, and a mean Ki67 labeling index of 1.71%. Conjunctival melanoma revealed strong immunopositivity of tumor cells for HMB45, Melan A and S100 protein, and a Ki67 labeling index of 20%. In all cases, the conjunctival epithelium showed strong immunopositivity for pan-CK AE1∕AE3. All our cases (100%) had a favorable outcome after the surgical removal of the tumor. CONCLUSIONS: Any excision of a conjunctival pigmented lesion must be subject to a systematic immunohistopathological examination, and there is a set of antibodies (anti-HMB45 and anti-Ki67) that are useful for differential diagnosis between a conjunctival nevus and a conjunctival melanoma.


Subject(s)
Conjunctival Neoplasms , Melanoma , Nevus, Pigmented , Skin Neoplasms , Adolescent , Child , Conjunctival Neoplasms/diagnosis , Female , Humans , Ki-67 Antigen/metabolism , MART-1 Antigen/metabolism , Male , Melanocytes/metabolism , Melanocytes/pathology , Melanoma/pathology , Nevus, Pigmented/pathology , Retrospective Studies , S100 Proteins , Skin Neoplasms/pathology
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