Evidence map›Paper›PMID 39299200›Full record

ArticleInternational journal of surgery case reports2024

A case of retinoblastoma masquerading as endophthalmitis: Unusual presentation and clinicopathological correlation.

Ghadah M S AlQahtani, Hind M Alkatan, Saleh AlMesfer, Sahar Elkhamary, Azza M Y Maktabi

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Article in International journal of surgery case reports, 2024. The graph could read no effect estimate from its abstract, so it casts no vote on the map. Not yet cited in PubMed.

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4 · The record

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5 · Who and what money

Authors and funding

5 authors.

Ghadah M S AlQahtaniFellowship and Residency Training Program, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
Hind M AlkatanDepartments of Ophthalmology and Pathology, College of Medicine, King Saud University, Riyadh, Saudi Arabia; King Saud University Medical City, King Saud University, Riyadh, Saudi Arabia.
Saleh AlMesferPediatric Ophthalmology and Strabismus Division, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia.
Sahar ElkhamaryRadiology department, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia; Diagnostic Radiology department, Mansoura University Hospital, Faculty of Medicine, Mansoura University, Egypt.
Azza M Y MaktabiPathology and Laboratory Medicine, King Khaled Eye Specialist Hospital, Riyadh, Saudi Arabia. Electronic address: amaktabi@kkesh.med.sa.

Funding

No grant is acknowledged in the PubMed record.

6 · The paper itself

Abstract

introductionRetinoblastoma is a serious childhood intraocular neoplasm that can be diagnosed clinically with the aid of B-scan ultrasound, and radiological examination. On the other hand, the differential diagnosis includes benign and other masquerading conditions such as uveitis and endophthalmitis thus adding challenge to the proper diagnosis. PRESENTATION OF CASE: A six-year-old girl presented with leukocoria and decreased vision of the right eye. Patient was diagnosed and treated as a case of endophthalmitis elsewherewith no improvement. She was re-evaluated in our hospital and found to have cataract with ruptured capsule, and no view to the fundus. B scan was conducted and showed posterior cavity mass with calcification, and retinal detachment. Retinoblastoma was suspected and proved by examination under anesthesia. Enucleation was carried out and the diagnosis was further confirmed by histopathological examination. DISCUSSION: Diagnosis of retinoblastoma can be challenging since leukocoria is the most common presenting complaint, which can be also seen in other benign conditions such as Coat's disease. It may also masquerade as endophthalmitis, uveitis with or without glaucoma, and retinal detachment. High suspicious of retinoblastoma in children and appropriate examination and work up with the aid of Biomicroscopy and radiological examination will help reaching the appropriate diagnosis saving patients unnecessary interventions with related morbidity.

conclusionRetinoblastoma has a wide spectrum of clinical presentations and must be ruled out before performing any intraocular procedure.

Indexed as

Case reportEndophthalmitisIntravitreal injectionMasqueradeRetinoblastomaUveitis

Identifiers

PMID39299200
PMCPMC11424937

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