What is the likelihood of Central Serous Chorioretinopathy (CSC) developing into Choroidal Neovascularization (CNVM)?

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Last updated: August 26, 2025View editorial policy

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Likelihood of Choroidal Neovascularization Development in Central Serous Chorioretinopathy

Choroidal neovascularization (CNV) develops in approximately 2-18% of patients with chronic central serous chorioretinopathy (CSC), with higher risk in older patients and those with prolonged disease. 1

Risk Factors for CNV Development in CSC

  • Age: Higher risk in patients over 50 years
  • Disease duration: Prolonged CSC increases risk
  • Disease severity: More common in severe chronic CSC
  • Treatment history: Laser photocoagulation can increase risk of iatrogenic CNV 2

Clinical Features Suggesting CNV in CSC

  • Mid/hyperreflective signal below a flat irregular retinal pigment epithelial detachment (FIPED) on OCT
  • Well-demarcated CNV "plaque" (with or without polypoidal component) on indocyanine green angiography (ICGA)
  • Presence of a vascular network on optical coherence tomography angiography (OCT-A) 1

Diagnostic Challenges

  • CNV can be present at the onset of CSC or develop gradually
  • Detection can be challenging in small, early-stage CNV
  • Up to two-thirds of CSC patients with CNV may have a polypoidal component, making ICGA particularly valuable for identification 1
  • "Silent type 1 CNV" may be common in chronic CSC but only detectable on OCT-A 1

Prognosis and Clinical Course

  • CNV detection occurs on average 1.65 ± 2.30 years after CSC diagnosis 3
  • Most patients (73.3%) remain stable for more than 6 months without subretinal fluid recurrence after appropriate treatment
  • Visual outcomes are generally favorable with proper management
  • Some patients (20%) may not require treatment during observation 3

Management of CSC with CNV

  • First-line treatment: Intravitreal anti-VEGF injections for active CNV 1
  • Adjunctive therapy: Half-dose or half-fluence photodynamic therapy (PDT) may be combined with anti-VEGF 1
  • Polypoidal component: If present, combination of PDT and anti-VEGF shows better results than monotherapy 1

Important Considerations

  • Regular monitoring with multimodal imaging (OCT, FA, ICGA, OCT-A) is essential for early detection of CNV in chronic CSC
  • "Silent type 1 CNV" may not require immediate treatment until active leakage becomes evident 1
  • CNV secondary to CSC generally has better prognosis than CNV from age-related macular degeneration 3

Pitfalls to Avoid

  • Misdiagnosis of CNV as uncomplicated CSC, especially in older patients
  • Overlooking small CNV in patients with extensive chorioretinal abnormalities
  • Failure to use multimodal imaging, particularly OCT-A and ICGA, which are crucial for detecting CNV in CSC
  • Delaying treatment in cases with active CNV, which can lead to worse visual outcomes

Regular follow-up with comprehensive multimodal imaging is essential for patients with chronic CSC to detect CNV development early and initiate appropriate treatment promptly.

Professional Medical Disclaimer

This information is intended for healthcare professionals. Any medical decision-making should rely on clinical judgment and independently verified information. The content provided herein does not replace professional discretion and should be considered supplementary to established clinical guidelines. Healthcare providers should verify all information against primary literature and current practice standards before application in patient care. Dr.Oracle assumes no liability for clinical decisions based on this content.

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