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A Non-invasive Way to Isolate and Phenotype Cells from the Conjunctiva
Published on: July 5, 2017
Benign reactive lymphoid hyperplasia of the conjunctiva in childhood
Adel G AlAkeely1, Hind M Alkatan2,3, Adel H Alsuhaibani2
1King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
Insights
This study details benign reactive lymphoid hyperplasia (BRLH) in children, finding it has a benign clinical course with rare recurrence. Paediatric conjunctival BRLH in children shows a favorable prognosis.
Area of Science:
- Ophthalmology
- Pediatric Oncology
- Pathology
Background:
- Benign reactive lymphoid hyperplasia (BRLH) of the conjunctiva is a rare condition in children.
- Understanding its clinical and histopathological features is crucial for accurate diagnosis and management.
Purpose of the Study:
- To report the clinical and histopathological features of conjunctival BRLH in pediatric patients.
- To evaluate the outcomes of treatment and recurrence rates for this condition.
Main Methods:
- Retrospective chart review of pediatric patients (0-18 years) diagnosed with conjunctival BRLH between 2000 and 2013.
- Data collection included demographics, lesion characteristics, histopathology, and treatment outcomes.
- Molecular genetic studies were analyzed where available.
Main Results:
- Twenty-four cases of conjunctival BRLH were identified, with a mean age of 11.6 years and a strong male predominance (96%).
- Lesions were typically unilateral, located on the bulbar conjunctiva, and predominantly nasal (96%).
- Despite two cases showing monoclonality suggestive of lymphoma, histopathology and clinical course confirmed BRLH; no infectious etiology was found.
Conclusions:
- Pediatric conjunctival BRLH follows a benign clinical course with no local or systemic spread.
- Recurrence of conjunctival BRLH is rare and was not associated with malignant transformation in this cohort.
Background/Aim:
Our aim is to the report the clinical and histopathological features of benign reactive lymphoid hyperplasia (BRLH) of the conjunctiva in children and the outcomes of treatment.
Methods:
A retrospective chart review was performed for children aged 0-18 years, diagnosed with conjunctival BRLH from January 2000 to December 2013 at two large ophthalmology hospitals in the Middle East. Data were collected on patient demographics, features of the lesions, the site of the lesion, location, adnexal involvement, lymph nodes involvement, local spread, histopathology and molecular genetic studies of the cases (if available), outcomes of treatment and recurrence.
Results:
There were 24 patients with lymphoid lesions classified as conjunctival BRLH during the 12-year period evaluated in this study. The mean age at diagnosis was 11.6 years. Twenty-three patients were males (96%). Systemic medical history included three patients with bronchial asthma, one patient with Down's syndrome, one patient with generalised skeletal malformation and one patient with gastritis. The initial uncorrected visual acuity was 20/30 or better in 93.5% of the eyes. At presentation, the tumour was unilateral in 12 cases (50%). The conjunctival mass was located on the bulbar conjunctiva in all cases. The mass was present nasally in 96% of lesions. No cases (that were tested) had an infectious aetiology. PCR demonstrated monoclonality suggestive of lymphoma in two cases; however, this did not alter the final diagnosis as BRLH per histopathological criteria and clinical course, CONCLUSIONS: All investigated cases of paediatric conjunctival BRLH had a benign clinical course with no local or systemic dissemination and a male predominance. Recurrence was rare, and in our cohort, it was not associated with malignant transformation.
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