THE RAP STUDY, REPORT TWO: The Regional Distribution of Macular Neovascularization Type 3, a Novel Insight Into Its

Bilal Haj Najeeb1, Gabor Deak, Ursula Schmidt-Erfurth

  • 1Vienna Reading Center, Department of Ophthalmology, Medical University of Vienna, Vienna, Austria.

Abstract

Insights

Macular neovascularization type 3 (MNV3) lesions are not uniformly distributed. These MNV3 lesions show a radial distribution preference in the temporal perifoveal area.

Area of Science:

  • Ophthalmology
  • Retinal Diseases
  • Neovascularization

Background:

  • Macular neovascularization (MNV) is a key feature in several retinal diseases.
  • Understanding the specific distribution patterns of different MNV types is crucial for diagnosis and treatment.
  • Macular neovascularization type 3 (MNV3) represents a distinct subtype with potentially unique epidemiological characteristics.

Purpose of the Study:

  • To investigate the regional distribution of macular neovascularization type 3 (MNV3) in the macula.
  • To determine if MNV3 lesions exhibit a specific spatial pattern or preference.
  • To assess the relationship between MNV3 distribution and the foveal avascular zone (FAZ).

Main Methods:

  • Retrospective review of 78 eyes from 78 patients diagnosed with MNV3.
  • Lesion location was mapped using a modified ETDRS grid.
  • Analysis included incidence of simultaneous MNV1 or MNV2 and MNV3 distribution relative to the FAZ outline and diameter.

Main Results:

  • MNV3 lesions were predominantly located between 500 µm and 1500 µm from the center (92%).
  • Lesions showed a significant temporal distribution (40%), followed by inferior (31%), superior (20%), and nasal (9%).
  • Most MNV3 lesions radiated radially in the temporal perifoveal area (72%), with none found at the FAZ boundary.

Conclusions:

  • Macular neovascularization type 3 (MNV3) lesions are not symmetrically or uniformly distributed.
  • MNV3 demonstrates a clear tendency for radial distribution, particularly in the temporal perifoveal region.
  • The findings suggest specific pathogenetic mechanisms influencing MNV3 localization.