Purpose: Anti-neutrophil cytoplasmic antibody (ANCA)-associated vasculitis (AAV) is a necrotizing vasculitis syndrome characterized by the destruction of small vessels, leading to various organ disorders. Here, we report a case of posterior scleritis with AAV successfully treated with prednisolone and rituximab (RTX) combination therapy.
Observations: A 69-year-old female suffered from ocular pain and redness in her left eye for 2.5 years. She had been diagnosed with idiopathic otitis media before a year. At her initial visit, scleral injection with nodular elevated scleral lesions, vitreous haze, and serous retinal detachment (SRD) in the inferior periphery were observed in the left eye. Enhanced computed tomography revealed the enhancement and thickening of the left sclera. The results of laboratory analysis were positive for myeloperoxidase ANCA. Accordingly, she was diagnosed with AAV. Owing to the exacerbation of vitreous haze and SRD, topical treatment and steroid pulse therapy were initiated. Following therapy, anterior and posterior scleritis improved, and additional RTX was administered to maintain the remission. Following treatment, the patient has maintained remission with 10 mg/day prednisolone to date.
Conclusions And Importance: We encountered a case of posterior scleritis with AAV in which inflammatory manifestations subsided with RTX and glucocorticoid combination therapy. RTX administration likely contributed to the maintenance of remission.
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http://dx.doi.org/10.1016/j.ajoc.2022.101333 | DOI Listing |
iScience
December 2024
Tianjin Key Laboratory of Retinal Functions and Diseases, Tianjin Branch of National Clinical Research Center for Ocular Disease, Eye Institute and School of Optometry, Tianjin Medical University Eye Hospital, Tianjin, China.
Autoimmune uveitis and posterior scleritis are ocular diseases caused by immune dysregulation. Their pathogenesis remains elusive, and delayed diagnosis can exacerbate vision loss. Our study analyzed proteomic profiles of 190 patients with Behcet's disease uveitis, posterior scleritis, and Vogt-Koyanagi-Harada syndrome.
View Article and Find Full Text PDFCureus
November 2024
Ophthalmology, Ahmadi Hospital, Ahmadi, KWT.
Nodular posterior scleritis is an uncommon inflammatory disorder of the eye characterized by nodular lesions that may be similar to other intraocular conditions such as choroidal melanoma, leading to diagnostic difficulties. This case report and literature review aims to evaluate the demographics, modalities, treatment, and outcomes of nodular posterior scleritis. We describe a 41-year-old female patient who presented with diminished vision in her left eye.
View Article and Find Full Text PDFBMJ Case Rep
December 2024
Department of Ophthalmology, All India Institute of Medical Sciences, Bhubaneswar, Odisha, India
Oxf Med Case Reports
November 2024
Eye Research Center, Mashhad University of Medical Sciences, Khatam Al-Anbia Eye Hospital, Gharani Boulevard, Mashhad, Iran.
: To report a patient with choroidal bulging, sub-retinal fluid, and optic nerve head (ONH) swelling who was finally diagnosed with focal nodular posterior scleritis. : A 51-year-old male patient presented to us with acute painful visual loss of his left eye (LE) from 3 days ago. The best-corrected distance visual acuity (BCDVA) was 20/20 and hand motion (HM) for the right eye (RE) and LE, respectively.
View Article and Find Full Text PDFBr J Ophthalmol
November 2024
Department of Vitreoretina and Uveitis Services, LV Prasad Eye Institute GMR Varalakshmi Campus, Visakhapatnam, Andhra Pradesh, India.
Purpose: This study aimed to identify the various clinical characteristics and ocular imaging features of ocular toxoplasmosis (OT) in HIV patients.
Methods: Observational retrospective study of 52 eyes of 38 HIV patients with OT.
Results: 68% of patients were male.
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