Biomedical subjects
Publications and source records attributed to Ileana Zolog.
This is to show the case of a 40 year old patient, where a congenital retinal macro-vessel was found, the peculiarities of which are increased calibre, intersection of the macular area, arteriovenous shunts and lack of functional disturbances. The disease is rare and its lesional and functional stability is remarkable.
This is the description of the case of a 36 year old male, who developed a combined hamartoma of the pigment epithelium and retina in the left eye. The location of the lesion in the macular zone, as well as the peculiar aspect of disease, raised some issues related to differential diagnosis. Attention was paid to the diseases of the posterior pole of eyeball, which, given their aspect of disease, result of a secondary hyperplastic reaction of the EPR, can embody a type of combined pseudohamartoma: retraction syndrome, retinal angiomatosis, pseudohistoplasmosis and others. A 5 years clinical supervision of the patient didn't show major changes.
This is the case of a 45 year man, with diffuse retinal epitheliopathy. The diagnosis was based on the angiofluorographic triad--diffusion sites; triangular lesions of the EPR, located vertically; serous detachments of the EPR. The therapy consisting of photocoagulation of the diffusion sites and of the harmed areas of the EPR led to a standstill of the clinical evolution, during a one year follow up period.
There are described a number of 9 clinical cases with unilateral myelinated nerve fibers, associated with myopia or amblyopia. Four cases developed extended myelinated areas, anisometropia with increased values, accentuated amblyopia and macular changes. Patients underwent treatment for amblyopia through correction with spectacles lenses and the occlusion of the congenerous eye. The obtained functional results differentiated the casemix in two groups: with therapeutic failure, 4 cases, characterized by extended myelination, anisometropia with an average of over -10 diopters and macular changes. with therapeutic success, 5 cases, characterized by reduced myelination, anisometropia with an average of over -4 diopters and normal maculae. It has been found a significantly statistical difference between the two groups as regarding the value of the anisometropia. However, the macular aspect has been an important factor in order the therapeutic effect to succeed. This clinical syndrome is differentiated from the unilateral simple myopia with amblyopia and from the myelinated nerve fibers without myopia or amblyopia.