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Implantation and Evaluation of Melanoma in the Murine Choroid via Optical Coherence Tomography
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Choroid Melanoma - A Rare Case Report.

Samarth Shukla1, Sourya Acharya2, Manisha Dulani3

  • 1Professor, Department of Pathology, J N Medical College, DMIMS Univ , Sawangi (Meghe), Wardha, Maharashtra, India .

Journal of Clinical and Diagnostic Research : JCDR
|July 9, 2015
PubMed
Summary

Choroid melanoma, the most common adult intraocular malignancy, originates from uveal tract melanocytes. This case highlights a rare occurrence in a 65-year-old presenting with vision loss and headache.

Keywords:
Ciliary bodyIrisMalignancyUveal

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Area of Science:

  • Ophthalmology
  • Oncology

Background:

  • Uveal tract melanomas include iris, ciliary body, and choroid.
  • Choroid melanomas are the most frequent intraocular malignancies in adults, though rare overall.
  • The global incidence is approximately 20 cases per million annually.

Observation:

  • Melanomas arise from pigment-producing melanocytes within the uveal tract.
  • Onset typically occurs in the sixth decade, with incidence increasing with age.
  • A rare case of choroidal melanoma is presented in a 65-year-old adult.

Findings:

  • The patient presented with a three-month history of headache and progressive vision dimming.
  • Clinical diagnosis confirmed choroid melanoma.
  • Enucleation was performed as treatment.

Implications:

  • This case underscores the importance of considering choroidal melanoma in adult patients with unexplained vision loss and headaches.
  • Early diagnosis and treatment are crucial for managing intraocular malignancies.
  • Further research into the origins and progression of uveal melanomas may improve patient outcomes.