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Biomedical subjects

Paul Sanfilippo

Publications and source records attributed to Paul Sanfilippo.

7 recordsLinked to original sources

Optical coherence tomography of adult-onset fovemacular vitelliform dystrophy.

Adult-onset foveomacular vitelliform dystrophy is characterized by a focal, round or oval shaped, subretinal foveal yellow lesion that presents bilaterally and usually symmetrically in the fourth or fifth decade of life. In addition to clinical observation, diagnosis of the disease process has until now been assisted by electrophysiological and fundus fluorescein studies. Two cases are presented that correlate the clinical fundus appearance with optical coherence tomography findings and describe the location of the yellow vitelliform material.

Aged↗

Pellucid marginal degeneration and scleroderma.

Systemic scleroderma is a progressive multi-system connective tissue disease. Ocular involvement includes keratoconjunctivitis sicca, progressive shallowing of conjunctival fornices, peripheral ulcerative keratitis and eyelid tightness. No association has been reported between scleroderma and pellucid marginal degeneration, which is a rare bilateral corneal ectasia. Pellucid marginal degeneration is characterised by non-inflammatory and progressive peripheral corneal thinning inferiorly, often with high against-the-rule astigmatism. We report a case of a 55-year-old woman with systemic scleroderma who presented with rapidly progressing against-the-rule astigmatism. The differential diagnosis of peripheral corneal thinning and the challenge of the surgical management of pellucid marginal degeneration are briefly discussed.

Astigmatism↗

Management of filamentary keratitis associated with aqueous-deficient dry eye.

PURPOSE: To review the incidence, underlying pathophysiology, and clinical features of filamentary keratitis and to identify evidence-based best-practice strategies for managing filamentary keratitis. METHODS: A comprehensive review of published literature was undertaken. Recommendations for best-practice management strategies were based on the available evidence. Three cases are presented to illustrate the clinical findings and management of patients with chronic filamentary keratitis. RESULTS: Although the evidence base is limited by the absence of well-designed studies, current evidence indicates the following: (1) Aqueous-deficient dry eye (keratoconjunctivitis sicca) is the most common ocular condition associated with filamentary keratitis. (2) Current best-practice management of filamentary keratitis involves treating the underlying dry eye and specific treatments for the corneal filaments. Proposed treatments include nonpreserved lubricants, topical steroidal and nonsteroidal anti-inflammatory agents, and punctal plugs for aqueous-deficient dry eye as well as mechanical removal of filaments, hypertonic saline, mucolytic agents, and bandage contact lenses for the filaments. (3) Filamentary keratitis can be induced or exacerbated by contact lens wear and ocular surgical procedures such as cataract surgery and corneal graft surgery. Pre- and postoperative ocular surface management strategies should be considered in the surgical planning of patients with, or who are susceptible to, filamentary keratitis. Filamentary keratitis can also be induced and/or exacerbated by chronic use of ocular and/or systemic medications, and alternate medications or additional measures to manage the tear film and ocular surface may be required in these cases. CONCLUSIONS: Filamentary keratitis can be a chronic, recurrent, and debilitating condition. With a systemic approach to diagnosis and management, the condition can be effectively controlled and the incidence and severity of recurrences minimized.

Adult↗

Ocular cicatricial pemphigoid.

Ocular cicatricial pemphigoid is a chronic progressive immunological disease, although acute inflammatory episodes may occur. Typically, it leads to fornix foreshortening, symblepharon and dry eye problems. In the end stage, the cornea is severely affected, resulting in serious vision loss. We report on the diagnosis and management of a patient with ocular cicatricial pemphigoid and comment on the differential diagnosis, complications and treatment options.

Conjunctivitis↗

Retinal angioma associated with von Hippel-Lindau disease.

Von Hippel-Lindau disease is a multi-system disorder that can produce hamartomas (benign tumour-like nodules) of the eyes, skin and nervous system. Retinal capillary angioma is a common ocular association of this congenital phakomatosis that may result in blinding sequelae, if not managed appropriately. We present a case of retinal angioma associated with von Hippel-Lindau disease and discuss the ocular and systemic signs, diagnosis and management. The optometrist is of particular importance in screening for this disorder, as it is often first detected in a routine eye examination.

Adult↗

A case of preseptal cellulitis.

Infection of the eyelids confined to the preseptal space is relatively common but potentially serious. It occurs with much greater frequency than do orbital infections and if left untreated, it has the potential to be life-threatening. We present a classic case of preseptal cellulitis and discuss how the optometrist can be involved in the diagnosis and management of this infectious disorder.

Amoxicillin↗

A review of argon and selective laser trabeculoplasty as primary treatments of open-angle glaucoma.

It is generally accepted within the ophthalmic community that medical therapy is the preferred primary treatment in open-angle glaucoma, followed by laser trabeculoplasty if the medical therapy is unsuccessful, with surgery employed more as an end-stage option when these avenues have been exhausted. This review discusses the efficacy of argon laser trabeculoplasty, alone and in comparison with medical therapy as a primary treatment of glaucoma. It will also discuss the new laser technique, selective laser trabeculoplasty.

Journal Article↗