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1.
Eye Contact Lens ; 49(12): 572-574, 2023 Dec 01.
Article in English | MEDLINE | ID: mdl-37728867

ABSTRACT

INTRODUCTION: This report highlights a postinfectious mucocutaneous inflammatory response involving the ocular surface and adnexa after Chlamydophila psittaci exposure. CASE DESCRIPTION: A 35-year-old man presented after a prodrome of upper respiratory symptoms with rash and mucocutaneous blistering involving the ocular and oral mucosa, causing pseudomembranous conjunctivitis and corneal epithelial defects. Extensive inflammatory and infectious workup suggested recent C. psittaci infection. The patient was treated with doxycycline and supportive therapy, whereas the ocular surface was treated with lubrication and prophylactic antibiotics. In follow-up, he has retained excellent visual acuity but required scleral contact lenses to control ocular surface symptoms because of fibrotic changes of the marginal conjunctiva. DISCUSSION: Such blistering inflammation has most commonly been described after pediatric respiratory infections because of Mycoplasma pneumoniae with additional instances related to Chlamydia pneumoniae , Epstein-Barr virus, influenza B, and other stimuli . To the best of our knowledge, this is the first reported case of C. psittaci- induced reactive infectious mucocutaneous eruption (RIME). RIME is a rare parainfectious inflammatory condition with sequelae frequently involving the periocular mucosa. Although systemic and nonocular adverse outcomes in this condition tend to be self-limited, the impact on the ocular surface may be severe, and the consequences to vision may be ongoing, especially if not treated aggressively at the outset.


Subject(s)
Chlamydophila psittaci , Epstein-Barr Virus Infections , Exanthema , Eye Neoplasms , Psittacosis , Male , Humans , Child , Adult , Epstein-Barr Virus Infections/complications , Herpesvirus 4, Human , Psittacosis/complications , Psittacosis/diagnosis , Exanthema/complications
2.
J Pediatr Ophthalmol Strabismus ; 60(4): e35-e37, 2023.
Article in English | MEDLINE | ID: mdl-37478202

ABSTRACT

A 2-year-old girl with severe muscular dystrophy presented with unilateral eye pain and corneal clouding. She was found to have absent red reflex, hypotonia, cerebral hypoplasia, and iris bombe on ultrasound biomicroscopy, a feature not previously reported in this syndrome. She responded favorably to surgical management. Iris bombe can be a cause of glaucoma in muscle-eye-brain disease. This highlights the importance of incorporating ultrasound biomicroscopy into the diagnostic algorithm of muscle-eye-brain disease and other types of congenital syndromic glaucoma. [J Pediatr Ophthalmol Strabismus. 2023;60(4):e35-e37.].


Subject(s)
Glaucoma , Iris Diseases , Walker-Warburg Syndrome , Female , Humans , Child, Preschool , Iris/surgery , Iris/abnormalities , Walker-Warburg Syndrome/complications , Iris Diseases/diagnosis , Iris Diseases/surgery , Glaucoma/diagnosis , Glaucoma/etiology , Glaucoma/surgery , Microscopy, Acoustic
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