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Correspondence
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- Correspondence
Delayed-onset abducens nerve palsy following parafalcine meningioma complicated by subdural hematoma
Canadian Journal of OphthalmologyVol. 57Issue 4e136–e137Published online: December 28, 2021- Sami Younes
- Subahari Raviskanthan
- Peter W. Mortensen
- Andrew G. Lee
Cited in Scopus: 0Meningiomas are slow-growing, benign brain tumors accounting for approximately 20% of primary intracranial masses.1 They may remain asymptomatic for long periods of time and can present with headaches, seizures, and other more site-specific symptoms. Although they are highly vascular structures, meningiomas do not typically produce subdural hematoma (SDH).2 Only 38 cases of meningioma associated with acute SDH have been reported in the English literature.1 We report a delayed-onset abducens nerve palsy due to an SDH associated with a parafalcine meningioma. - Correspondence
Delayed diagnosis of autosomal dominant optic atrophy until seventh decade of life
Canadian Journal of OphthalmologyVol. 57Issue 3e96–e100Published online: September 14, 2021- Subahari Raviskanthan
- Pranati Ahuja
- Peter W. Mortensen
- Dan Milea
- Andrew G. Lee
Cited in Scopus: 0Autosomal dominant optic atrophy (ADOA) is the most common hereditary optic neuropathy, manifesting in approximately 1 in 50 000 people, and up to 1 in 10 000 in Denmark, owing to a founder mutation.1 Isolated ADOA typically manifests in the first 2 decades of life as bilateral painless progressive vision loss and is therefore mostly diagnosed in childhood to young adulthood. We present a series of 2 older patients, aged 63 and 64 years, who had delayed ADOA diagnosis as proband patients in their families, emphasizing the point that chronological age should not be the sole determining factor for ordering testing for ADOA in cases of unexplained optic neuropathy. - Correspondence
Superior oblique myositis following targeted therapy for papillary thyroid carcinoma
Canadian Journal of OphthalmologyVol. 56Issue 4e125–e127Published online: February 16, 2021- Alexander M. Tseng
- Enoch T. Peng
- Shruthi H Bindiganavile
- Subahari Raviskanthan
- Nita Bhat
- Peter W. Mortensen
- and others
Cited in Scopus: 1Papillary carcinoma of the thyroid gland (PCTG) constitutes 80%–85% of thyroid cancers globally. Despite early lymphatic invasion, PCTG has a relatively indolent course and rarely metastasizes outside of the neck.1 Metastasis to the brain from PCTG is even more uncommon and usually occurs in the context of widely disseminated disease. While the mainstay of treatment for intracranial metastasis from PCTG includes surgical excision and radiotherapy, recent advances into our understanding of the molecular pathways governing PCTG have facilitated development of novel targeted chemotherapeutics.