A5019905388- Ocular Diseases and Behçet’s Syndrome
- Ocular Infections and Treatments
- Retinal and Optic Conditions
- Retinal Diseases and Treatments
- Vasculitis and related conditions
- Dermatological and Skeletal Disorders
- Inflammasome and immune disorders
- Drug-Induced Ocular Toxicity
- Cerebrovascular and Carotid Artery Diseases
- Herpesvirus Infections and Treatments
- Peripheral Artery Disease Management
- Salivary Gland Disorders and Functions
- HIV Research and Treatment
- Renal Diseases and Glomerulopathies
- Neurological Complications and Syndromes
- Syphilis Diagnosis and Treatment
- Sinusitis and nasal conditions
- Glaucoma and retinal disorders
- Reproductive tract infections research
- Genetic Neurodegenerative Diseases
- Neutrophil, Myeloperoxidase and Oxidative Mechanisms
- Retinal Development and Disorders
- Cerebral Venous Sinus Thrombosis
- interferon and immune responses
- HIV-related health complications and treatments
Vall d'Hebron Hospital Universitari
2020-2025
Hebron University
2024-2025
To report the successful use of internal limiting membrane peeling, inverted flap and plasma rich in growth factors bilateral full-thickness macular hole Behçet's disease. A comprehensive multimodal ophthalmological examination, including optical coherence tomography, fluorescein angiography indocyanine angiography, was conducted along with a multidisciplinary approach. An individualized systemic immunosuppressive treatment initiated, surgical planned both eyes. 29-year-old patient full...
Abstract Purpose To report a case of Purpureocillium lilacinum endophthalmitis. Methods The fungal endophthalmitis caused by documented in an immunocompetent patient with no apparent trigger. Results A 64-year-old male two-month history panuveitis his left eye was referred to our hospital. Initially misdiagnosed as sympathetic ophthalmia due previous surgery on right 4 months before the onset ocular picture, received corticosteroid treatment, leading rapid deterioration condition. An urgent...
Purpose To investigate the rare manifestation of retinal vasculitis in Familial Mediterranean fever (FMF) and its correlation with specific gene mutations, particularly MEFV gene, a focus on severity phenotypes systemic vasculitis.
<title>Abstract</title> <bold>PURPOSE</bold> To report a case of <italic>Purpureocillium lilacinum </italic>endophthalmitis <bold>METHODS</bold> The fungal endophthalmitis caused by lilacinum</italic> documented in an immunocompetent patient with no apparent trigger. <bold>RESULTS</bold> A 64-year-old male two-month history panuveitis his left eye was referred to our hospital. Initially misdiagnosed as sympathetic ophthalmia due previous surgery on right 4 months before the onset ocular...
<h3>Background:</h3> Primary Sjögren's Syndrome (pSS) is an autoimmune disease characterized by dryness of mucous membranes, especially the eyes and mouth, infiltration affected tissues lymphocytes. The Oxford grading scale (OGS) evaluates corneal damage that can be associated with dry eye disease. measurement ocular surface part ACR-EULAR 2016 classification criteria, using Ocular Staining Score (OSS) or van Bijsterveld score (vBs). Although OGS not considered within these this test could...
To describe a rare case of posterior scleritis associated with late-onset Takayasu arteritis.
Gonococcus (GC) is considered one of the most prevalent STIs worldwide. We report a case gonococcal ocular infection (GOI) in 40-year-old man. He consulted for 4-week history unilateral purulent conjunctivitis and severe pain, after experimenting clinical worsening despite having been treated viral conjunctivitis. On examination, visual acuity (VA) was 20/63, superior corneal perforation with iris prolapse observed. After directed history, he revealed high-risk sexual behaviour within last 3...