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Correspondence
6 Results
- Correspondence
Superior limbic keratoconjunctivitis following ptosis repair
Canadian Journal of OphthalmologyVol. 57Issue 5e173–e175Published online: February 3, 2022- Khizar Rana
- Valerie Juniat
- Hokoru Yoshioka
- Mark Chehade
- Christopher M. Stewart
- Akihide Watanabe
- and others
Cited in Scopus: 0Superior limbic keratoconjunctivitis (SLK) is an inflammatory condition of the superior bulbar conjunctiva, tarsal conjunctiva, and upper cornea of unknown etiology. The pathogenesis of SLK is unclear, although it has been linked to mechanical microtrauma, deficiencies in tear film quality, and immunologic dysregulation.1 - Correspondence
Traumatic direct carotid cavernous fistula following partial maxillectomy
Canadian Journal of OphthalmologyVol. 57Issue 5e171–e172Published online: February 1, 2022- Medhir Kumawat
- Valerie Juniat
- Michelle T. Sun
- Nicholas Bajic
- Dinesh Selva
Cited in Scopus: 0Carotid cavernous fistula (CCF) is a rare traumatic complication that can occur following iatrogenic interventions.1 We report a case of direct CCF (type A) developing following partial maxillectomy with the Le Fort I approach. This case report adheres to the ethical principles outlined in the Declaration of Helsinki as amended in 2013. - Correspondence
Importance of correlating radiohistopathologic features in lacrimal gland pleomorphic adenoma
Canadian Journal of OphthalmologyVol. 57Issue 4e141–e142Published online: October 27, 2021- Raghav Goel
- Valerie Juniat
- Sophia Otto
- James Slattery
- Dinesh Selva
Cited in Scopus: 0Lacrimal gland pleomorphic adenoma (LGPA) is a common benign epithelial tumour of the lacrimal gland that frequently appears on imaging as a well-circumscribed lesion with no bony erosion.1 In some cases, it can present with atypical radiologic features and then needs to be correlated with histopathologic findings to ascertain a diagnosis. - Correspondence
Corneal limbal xanthogranuloma in Erdheim-Chester disease
Canadian Journal of OphthalmologyVol. 57Issue 3e87–e89Published online: October 26, 2021- Brad Guo
- Valerie Juniat
- Amardeep Gilhotra
- Dinesh Selva
Cited in Scopus: 0Adult orbital xanthogranulomatous disease is a rare non-Langerhans cell histiocytic condition with 4 clinical subtypes: adult‐onset xanthogranuloma, adult‐onset asthma with periocular xanthogranuloma, necrobiotic xanthogranuloma (NBX), and Erdheim–Chester disease (ECD). We report, to our knowledge, the first case of ECD with limbal infiltration. - Correspondence
Conservative management of periorbital necrotizing fasciitis caused by methicillin-resistance Staphylococcus aureus
Canadian Journal of OphthalmologyVol. 56Issue 3e86–e88Published online: November 5, 2020- Cassie A. Cameron
- Valerie Juniat
- Marcus Pyragius
- Dinesh Selva
Cited in Scopus: 1Necrotizing fasciitis (NF) of the periorbital region is a rare occurrence, though has been shown to cause severe facial disfigurement, blindness, and death.1,2 We report a case of community-acquired methicillin-resistant Staphylococcus aureus (MRSA)–associated periorbital NF in a 25-year-old woman, who presented with left eye and nostril redness and swelling after picking a pimple on her nose a few days prior. She had no significant medical history and was not diabetic. She was initially diagnosed with facial cellulitis and commenced on antibiotics, but returned 2 days later with worsening cellulitis, bilateral leg pain and redness, and shortness of breath. - Correspondence
Pachymeningeal enhancement on magnetic resonance imaging in granulomatosis with polyangiitis
Canadian Journal of OphthalmologyVol. 55Issue 5e181–e182Published online: May 19, 2020- Bobak Bahrami
- Valerie Juniat
- Garry Davis
- Dinesh Selva
Cited in Scopus: 1Granulomatosis with polyangiitis (GPA) is a multisystemic, antineutrophil cytoplasmic antibody (ANCA)–associated small vessel vasculitis. The orbit and ocular tissues are implicated in approximately a third of cases.1 Common manifestations are conjunctivitis, episcleritis, orbital inflammation, and uveitis.1