Difficultés diagnostiques face à une tumeur papillaire pigmentée. À propos d’un cas
| Autor: | L. Agnaou, Z. Chaoui, M Charif Chefchaouni, Amina Berraho, Z. Hajji |
|---|---|
| Rok vydání: | 2005 |
| Předmět: |
Optic nerve tumor
medicine.medical_specialty genetic structures medicine.diagnostic_test business.industry Fundus (eye) Fluorescein angiography medicine.disease Optic Nerve Neoplasm eye diseases Surgery Optic neuropathy Ophthalmology medicine.anatomical_structure medicine Optic nerve sense organs Melanocytoma business Optic disc |
| Zdroj: | Journal Français d'Ophtalmologie. 28:614-617 |
| ISSN: | 0181-5512 |
| DOI: | 10.1016/s0181-5512(05)81104-0 |
| Popis: | Melanocytoma of the optic disc is a benign pigmented tumor located on the optic nerve head. Most cases are visually asymptomatic but in rare cases it can cause visual loss, which does not necessarily involve malignant transformation. We present a case of melanocytoma in a 49-year-old woman who presented with decreased vision in her left eye. The pigmented mass was in close continuity with the juxtapapillary adjacent choroid. Fluorescein angiography demonstrated hypofluorescence with adjacent disc edema. Ultrasonography disclosed a high internal reflectivity mass in the optic nerve head without retrobulbar extension. Magnetic resonance imaging (T1 weighted images) disclosed a hyperintense signal on the optic nerve head. The tumor was stationary for 20 months. This report emphasizes problems differentiating a melanocytoma from malignant melanoma of the optic nerve. Unusual features of melanocytoma (superior nasal location in the optic disc with an adjacent choroidal component, a decrease in visual acuity and disc edema surrounding the tumor) are discussed. Visual loss can be induced by optic neuropathy or retinal vascular obstruction. Melanocytomas grow very slowly over several years or remains stable, in contrast to malignant melanoma. In suspicious cases, close follow-up with serial fundus photographs is essential, although malignant transformation is exceptional. |
| Databáze: | OpenAIRE |
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