ISSN: 2155-9570
Department of Ophthalmology, Oslo University Hospital, Oslo, Norway
Case Report
A 47-Year-Old Woman with a History of Tularemia and Regression of an Untreated Juxtapapillary Amelanotic Choroidal Malignant Melanoma More than Four Decades Following Initial Diagnosis
Author(s): Nils Andreas Eide, Per Syrdalen and Jesintha Navaratnam*
Background: We report a case of a symptomatic small Uveal Melanoma (UM) followed for 4 decades, the most
common primary intraocular tumor that regressed almost completely after an infectious disease, Tularemia, caused
by Francisella tularensis.
Case presentation: In 1981, a 47-year old nurse was diagnosed with a left-sided amelanotic juxtapapillary lesion
presumed to be a melanoma. In 1985, the visual acuity decreased to 0.5. The tumor became increasingly pigmented
and Sub-Retinal Fluid (SRF) was observed. Ultrasound B-scan demonstrated findings characteristic of a UM.
Enucleation was not recommended due to small size and useful vision. The lesion was evaluated annually with
fundus images and ultrasound B-scan. In 1993, an epidemic nephropathy presented with anuria. The serum tests,
Immunoglobulin M (IgM) and IgG,.. View More»
DOI:
10.35248/2155-9570.23.14.963