CONJUNCTIVAL PYOGENIC GRANULOMA
Published 2023 - 27th ESCRS Winter Meeting
Reference: P144 | Type: Presented Poster & Poster Submission | DOI: 10.82333/p22b-p870
Authors: Salma Hassina* 1 , mohammed amine krichene 1 , hasnaoui ihssane 1 , chaimaa bardi 1 , lobna robbana 1 , TLEMCANI YOUNES 1 , louay serghini 1 , abdellah elhassan 1 , amina berraho 1
1ophtalmology B,CHU IBN SINA,RABAT,Morocco
Purpose
Setting
Methods
We report the case of a 6 year old boy with notion of trauma 5 months ago by vegetal thorn who presented to the emergency room with a conjunctival lesion on his right eyelid appeared for 4 months which was small and progressively increasing in size. The examination objective:vision was 7 / 10, a bright red mass, vascularized, with a large base on his right upper tarsal conjunctival
Results
Pyogenic granuloma presents as a nontender, fleshy, red, vascular lesion.The lesions are typically sessile or pedunculated, are dome-shaped, and vary from 1 to 10 mm in diameter. The mass is a collection of granulation tissue such as chronic inflammatory cells, fibroblasts, and endothelial cells of budding capillaries .Most pyogenic granulomas are asymptomatic .Pyogenic granulomas rarely resolve spontaneously. If they are asymptomatic, no treatment is necessary.
The response to topical therapies varies among patients from a decrease in size to full resolution or no effect at all. Topical corticosteroids prescribed 4 times a day for 1 to 2 weeks may reduce the lesions.However, there may be no response at all. If the lesion persists, surgical excision is required.Removal of a single pedunculated lesion is done using a shave excision and electrocautery. Recurrence is uncommon with surgical excision, but the risk rises when granulation tissue remains.
Conclusion