32 research outputs found

    Orbital Burkitt's Lymphoma: An Aggressive Presentation

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    Objective. To present the case of an aggressive orbital Burkitt's lymphoma. Methods. Chart review. Case Presentation. A 24-year-old Haitian man came to our clinic complaining of rapidly progressive right eye proptosis. On examination, a large friable exophytic mass with necrotic areas and exudative/hemorrhagic secretions was noted protruding from his right orbit. A biopsy revealed the characteristic “starry-sky” appearance of a Burkitt lymphoma. The patient died shortly after due to complications from systemic involvement. Discussion. This case is meant to raise physicians' awareness on the healthcare situation in some underdeveloped countries, emphasizing the importance of education in preventive medicine

    Presumed Sturge Weber Syndrome in a Haitian Boy: A Case of Delayed Diagnosis

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    Purpose. To report an untypical presentation of a presumed Sturge-Weber Syndrome (SWS), and to highlight the indispensable value of thorough clinical examination as primary means for proper diagnosis and management. Methods. Chart review. Results. A 7 year-old boy, with a long history of ocular symptoms and an unspecified ocular surgery, presents with a painful blind left eye. Based on clinical examination, the suspicion of SWS was raised. The presentation was not typical in the sense that no evident port-wine stain was observed on the face. However, facial asymmetry and gum discoloration were guiding clinical clues to pursue further investigations. Unfortunately, due to poor treatment response, the patient underwent enucleation. Tissue pathology revealed diffuse choroidal hemangiomas, consistent with the diagnosis of SWS. Conclusion. SWS presents with hamartomatous malformations and venous dilation affecting the skin, central nervous system and eye. The ocular involvement may vary, with the most common complications being glaucoma, buphthalmos and diffuse choroidal hemangiomas. This case report helps remind physicians of the importance of a thorough clinical examination, and highlights the ophthalmologists' responsibility of examining beyond the eye

    Are patients with thyroid orbitopathy deficient in selenium and/or vitamin D?

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    Selenium is a potent nutritional antioxidant that regulates reactive oxygen species and redox status in all tissues influencing inflammation and immune responses. A European study on mild Graves' orbitopathy showed that supplementation with selenium improved quality of life, reduced ocular involvement, and slowed progression of the disease. Vitamin D has been hypothesized to promote the maintenance of immune homeostasis and supplementation is thought to benefit patients with multiple sclerosis for example. The aim of the study is to determine whether serum selenium and vitamin D levels are low in patients with thyroid orbitopathy

    Evaluation of Horner Syndrome in the MRI Era.

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    To identify the etiologies of adult Horner syndrome (HS) in the MRI era using a targeted evaluation approach and to assess the value and yield of targeted imaging. A retrospective chart review was performed of 200 adult outpatients with HS, confirmed with cocaine eyedrop testing. Patients were divided into subgroups based on the presence or absence of symptoms and those who did or did not receive additional testing with hydroxyamphetamine drops. Imaging was obtained based on pharmacologic localization and/or clinical evaluation. The etiology of HS and the yield of imaging were determined in all subgroups. Imaging showed causative lesions in 24 of 179 (12.84%) imaged patients with HS, and 13 (69.0%) were determined "idiopathic." Of the patients who underwent testing with hydroxyamphetamine drops (132 patients), 86 had a postganglionic localization with an imaging yield of 8.1%, and 46 had preganglionic cause with an imaging yield of 21.7%. Fifty-three patients (26.5%) never noticed ptosis/anisocoria before examination, and the imaging yield in this subgroup was 2.8%. Eighteen of the 200 patients (9.0%) had serious pathology, including carotid artery dissection, brain, or neck mass, and 6 of these (31.6%) had acute symptoms and/or pain. HS is most often idiopathic with serious pathology being relatively infrequent. When determining etiology, the absence of symptoms is not predictive of the pathology. However, acute onset of symptoms and/or pain are possible indicators for serious pathology. Localizing the lesion using hydroxyamphetamine drops whenever obtainable and available is still an efficient way to target imaging evaluation

    A Longhorn-Induced Superior Orbital Fissure Syndrome: A Case Report

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    Superior orbital fissure syndrome is a rare condition with a well-defined clinical presentation. Key clinical features include ophthalmoplegia, ptosis, impaired extraocular muscle function, proptosis, and paresthesia of the frontal region. These symptoms arise from damage to the neurovascular contents in the fissure. Standard treatment protocol does not currently exist due to the rarity of the condition. Treatment options described include conservative observation, versus steroids or surgery
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