Different clinical presentations of persistent placoid maculopathy: a case series
Mickael Anjou1, Federico Bernabei2, Jeremie Villaret3
1Department of Ophthalmology, Hôpital Cochin, Assistance Publique-Hôpitaux de Paris, 27 rue du Faubourg Saint Jacques, Paris, 75014, France. mickael.anjou@aphp.fr.
Persistent placoid maculopathy, a rare bilateral chorioretinopathy, presents with diverse clinical manifestations. This case series highlights varied patient outcomes and treatment responses for this condition.
Area of Science:
- Ophthalmology
- Retinal Diseases
- Chorioretinopathy
Background:
- Persistent placoid maculopathy is a rare idiopathic bilateral chorioretinopathy.
- This condition is characterized by distinct ocular manifestations.
Purpose of the Study:
- To report diverse clinical presentations of persistent placoid maculopathy.
- To expand understanding of the ocular manifestations of this rare condition.
Main Methods:
- Retrospective case series analysis of four patients with persistent placoid maculopathy.
- Utilized ophthalmological examinations, multimodal imaging, and patient history.
- Included cases with associated giant cell arteritis and post-transplant immunosuppression.
Main Results:
- Case 1: Giant cell arteritis presentation with macular atrophy despite corticosteroids.
- Case 2: Developed type 2 choroidal neovascularization, improved with anti-VEGF therapy.
- Case 3: Submacular hemorrhage and subsequent choroidal neovascularization.
- Case 4: Vision recovery with corticosteroids during immunosuppressive therapy.
Conclusions:
- Persistent placoid maculopathy exhibits a wide spectrum of clinical presentations.
- Management strategies vary based on individual patient factors and complications.
- This series broadens the understanding of this rare chorioretinopathy.
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