Microrips of the retinal pigment epithelium in polypoidal choroidal vasculopathy

Kunihiro Musashi1, Akitaka Tsujikawa, Yasuhiko Hirami

  • 1Department of Ophthalmology, Kyoto University Graduate School of Medicine, Kyoto, Japan.

Abstract

Insights

Microrips of the retinal pigment epithelium (RPE) in polypoidal choroidal vasculopathy (PCV) are uncommon but typically resolve without complications. These RPE microrips show leakage on angiography but rarely lead to RPE tears.

Area of Science:

  • Ophthalmology
  • Retinal Diseases
  • Choroidal Neovascularization

Background:

  • Polypoidal choroidal vasculopathy (PCV) is a common cause of wet age-related macular degeneration.
  • Retinal pigment epithelium (RPE) abnormalities are characteristic of PCV.
  • Microrips of the RPE have not been extensively studied in the context of PCV.

Purpose of the Study:

  • To investigate the clinical features of RPE microrips in patients with PCV.
  • To understand the natural history and implications of RPE microrips in PCV.

Main Methods:

  • Retrospective case series analysis of 156 eyes from 136 PCV patients.
  • Utilized fluorescein angiography and indocyanine green angiography to examine RPE lesions.
  • Monitored microrips for resolution and development of RPE tears during follow-up.

Main Results:

  • RPE microrips were identified in 7.1% of PCV eyes (11 out of 156).
  • Microrips exhibited pinpoint leakage in early fluorescein angiography, pooling in the subretinal space later.
  • Resolution of microrips occurred in 90.9% of cases within an average of 3.0 months, with no RPE tears observed.

Conclusions:

  • RPE microrips are an infrequent finding in PCV.
  • These microrips generally have minimal clinical significance and a favorable prognosis.
  • RPE microrips in PCV typically resolve spontaneously without progression to RPE tears.