8_retinoblastoma

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Ophthalmic Tumours

Retinoblastoma (ICD‐O‐3 C69.2) Rules for Classification In bilateral cases, the eyes should be classified separately. The classification does not apply to complete spontaneous regression of the tumour. There should be histological confirmation of the disease in an enucleated eye. The following are the procedures for assessing T, N, and M categories: T categories Physical examination and imaging N categories Physical examination M categories Physical examination and imaging; examination of bone marrow and cerebrospinal fluid may enhance the accuracy of appraisal

Regional Lymph Nodes The regional lymph nodes are the preauricular, submandibular, and cervical lymph nodes.

TNM Clinical Classification T – Primary Tumour TX  Primary tumour cannot be assessed. T0  No evidence of primary tumour.

T1  Tumour confined to the retina with subretinal fluid no more than 5 mm from the base of any tumour, without retinal detachment T1a  No tumour in either eye is greater than 3 mm in largest dimension or located closer than 1.5 mm to the optic nerve or fovea T1b  At least one tumour is greater than 3 mm in largest dimension or located closer than 1.5 mm to the optic nerve or fovea. No retinal detachment or subretinal fluid beyond 5 mm from the base of the tumour T2  Tumours with vitreous or subretinal seeding or retinal detachment T2a  tumour with subretinal fluid more than 5 mm from the base of any tumour T2b  Tumour with vitreous and/or subretinal seeding T3  Severe intraocular disease T3a  Phthisis or prephthisis bulbi


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