1.Recurrent Unilateral Vogt-Koyanagi-Harada Disease with Posterior Scleritis.
Su Young MOON ; Won Tae YOON ; Sung Pyo PARK
Korean Journal of Ophthalmology 2015;29(5):352-354
No abstract available.
Adult
;
Female
;
Humans
;
Recurrence
;
Retina/*pathology
;
Scleritis/*complications/diagnosis
;
Tomography, Optical Coherence
;
Uveomeningoencephalitic Syndrome/complications/*diagnosis
2.A Case of Nodular Scleritis in Association With Behcet's Disease.
The Korean Journal of Internal Medicine 2001;16(1):47-49
Approximately 50 % of patients with scleritis are known to be associated with systemic connective tissue diseases or vasculitic diseases such as rheumatoid arthritis (RA), Wegener's granulomatosis, relapsing polychondritis, and systemic lupus erythematosus. The patients with scleritis in association with Behcet's disease (BD) have been rarely described in the literature. We report a 46-year-old female patient with BD who developed the nodular scleritis.
Anti-Inflammatory Agents, Non-Steroidal/therapeutic use
;
Behcet's Syndrome/drug therapy
;
Behcet's Syndrome/diagnosis*
;
Behcet's Syndrome/complications*
;
Case Report
;
Cyclophosphamide/therapeutic use
;
Drug Therapy, Combination
;
Female
;
Follow-Up Studies
;
Human
;
Middle Age
;
Prednisolone/therapeutic use
;
Scleritis/drug therapy
;
Scleritis/diagnosis*
;
Scleritis/complications*
3.Aspergillus fumigatus Scleritis Associated with Monoclonal Gammopathy of Undetermined Significance.
Dong Hyun JO ; Joo Youn OH ; Mee Kum KIM ; Jang Won HEO ; Jin Hak LEE ; Won Ryang WEE
Korean Journal of Ophthalmology 2010;24(3):175-178
A 68-year-old woman presented with pain in her left eye. Necrosis with calcium plaques was observed on the medial part of the sclera. Aspergillus fumigatus was isolated from the culture of the necrotic area. On systemic work-up including serum and urine electrophoresis studies, the serum monoclonal protein of immunoglobulin G was detected. The patient was diagnosed with monoclonal gammopathy of undetermined significance and fungal scleritis. Despite intensive treatment with topical and oral antifungal agents, scleral inflammation and ulceration progressed, and scleral perforation and endophthalmitis developed. Debridement, antifungal irrigation, and tectonic scleral grafting were performed. The patient underwent a combined pars plana vitrectomy with an intravitreal injection of an antifungal agent. However, scleral and intraocular inflammation progressed, and the eye was enucleated. Aspergillus fumigatus was isolated from the cultures of the eviscerated materials. Giemsa staining of the excised sclera showed numerous fungal hyphae.
Aged
;
Amphotericin B/administration & dosage
;
Antifungal Agents/administration & dosage
;
*Aspergillosis/therapy
;
*Aspergillus fumigatus
;
Disease Progression
;
Eye Enucleation
;
Female
;
Humans
;
Injections, Intraocular
;
Paraproteinemias/*complications
;
Sclera/pathology/ultrasonography
;
Scleritis/*complications/diagnosis/*microbiology/physiopathology
;
Vitrectomy
4.A Case of Necrotizing Keratoscleritis in Primary Sjogren's Syndrome.
Won CHOI ; Shin Seok LEE ; Yeong Geol PARK ; Kyung Chul YOON
Korean Journal of Ophthalmology 2011;25(4):275-277
We report on a case of necrotizing keratoscleritis in primary Sjogren's syndrome. A 66-year-old female patient who was complaining of ocular pain, tearing and decreased vision in her right eye for the previous two days was admitted to our hospital. Visual acuity in the right eye was hand movement, and initial examination showed a 3.0 x 1.8 mm uveal mass bulging through a corneoscleral melting site in the nasal region of the right eye. Positive anti-nuclear antibody was identified at a titer of 1:320 with a speckled pattern, and both Sjogren's syndrome A and Sjogren's syndrome B antibody tests were positive, with titers >200 U/mL. A technetium 99m pertechnetate salivary scan revealed chronic sialoadenitis in the submandibular glands. We diagnosed the lesion as necrotizing keratoscleritis due to primary Sjogren's syndrome. A corneoscleral patch graft was performed, followed by immunosuppression including oral cyclosporin and topical prednisolone. During a follow-up period of 12 months, the corneoscleral graft was well maintained with no recurrence.
Aged
;
Diagnosis, Differential
;
Disease Progression
;
Female
;
Follow-Up Studies
;
Glucocorticoids/administration & dosage
;
Humans
;
Keratitis/drug therapy/*etiology/pathology
;
Necrosis
;
Ophthalmic Solutions
;
Scleritis/drug therapy/*etiology/pathology
;
Sjogren's Syndrome/*complications/drug therapy/pathology
;
Visual Acuity