[Diagnostic potential of optical coherence tomography for small choroidal melanomas]

A F Brovkina1, A S Stoyukhina2, I V Musatkina1

  • 1Russian Medical Academy of Postgraduate Education, Ministry of Health of the Russian Federation, 2/1 Barrikadnaya St., Moscow, Russian Federation, 123995.

Vestnik Oftalmologii
|December 3, 2016
PubMed
Abstract

Insights

Optical coherence tomography (OCT) reveals early retinal changes in choroidal melanoma (CM) as it grows. These changes, including RPE and neuroepithelial detachment, precede significant tumor growth and lead to irreversible retinal distortion.

Area of Science:

  • Ophthalmology
  • Oncology
  • Medical Imaging

Background:

  • Choroidal melanoma (CM) is a rare intraocular malignancy.
  • Understanding the early signs of CM is crucial for timely diagnosis and treatment.
  • Optical coherence tomography (OCT) is a key imaging modality in ophthalmology.

Purpose of the Study:

  • To investigate the sequential optical coherence tomography (OCT) manifestations in choroidal melanoma (CM) correlated with tumor growth.
  • To characterize the early structural and functional changes in the retina overlying CM.

Main Methods:

  • Examined 28 patients with choroidal melanoma (CM) using OCT and fundus autofluorescence.
  • Categorized patients into early (18) and medium-sized (10) CM groups.
  • Analyzed tumor dimensions (prominence and basal diameter) and location (macular/perimacular).

Main Results:

  • Early OCT findings include choroidal profile changes, uneven configuration, and plateau formation.
  • Retinal pigment epithelium (RPE) and neuroepithelial detachment (NED) with photoreceptor layer alterations were observed.
  • Three types of photoreceptor damage were identified; destruction of all retinal layers signifies transition to medium-sized CM.
  • Autofluorescence revealed lipofuscin deposits (hyperautofluorescence) in RPE, hypoautofluorescence centrally, and peripheral hyperautofluorescence due to NED.

Conclusions:

  • Qualitative retinal changes in CM develop early, coinciding with initial choroidal profile shifts.
  • Retinal destruction initiates with RPE and neuroepithelium, progressing to irreversible architectural distortion, edema, and intraretinal deposits.
  • Tumor growth significantly alters metric parameters of retinal layers and the choroid.

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