| Literature DB >> 29915471 |
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Abstract
Entities:
Year: 2018 PMID: 29915471 PMCID: PMC5998398
Source DB: PubMed Journal: Community Eye Health ISSN: 0953-6833
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| cTX | Unknown evidence of intraocular tumour | |
| cT0 | No evidence of intraocular tumour | |
| cT1 | Intraocular tumour(s) with sub-retinal fluid ≤ 5mm from the base of any tumour | |
| cT1a | Tumours ≤ 3mm and further than 1.5 mm from the disc and fovea | |
| cT1b | Tumours > 3 mm or closer than 1.5 mm to the disc and fovea | |
| cT2 | Intraocular tumour(s) with retinal detachment, vitreous seeding or sub-retinal seeding | |
| cT2a | Sub-retinal fluid > 5 mm from the base of any tumour | |
| cT2b | Tumours with vitreous seeding and/or sub-retinal seeding | |
| cT3 | Advanced intraocular tumour(s) | |
| cT3a | Phthisis or pre-phthisis bulbi | |
| cT3b | Tumour invasion of the pars plana, ciliary body, lens, zonules, iris or anterior chamber | |
| cT3c | Raised intraocular pressure with neovascularization and/or buphthalmos | |
| cT3d | Hyphema and/or massive vitreous hemorrhage | |
| cT3e | Aseptic orbital cellulitis | |
| cT4 | Extraocular tumour(s) involving the orbit, including the optic nerve | |
| cT4a | Radiological evidence of retrobulbar optic nerve involvement or thickening of the optic nerve or involvement of the orbital tissues | |
| cT4b | Extraocular tumour clinically evident with proptosis and orbital mass | |
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| cNX | Regional lymph nodes cannot be assessed | |
| cN0 | No regional lymph nodes involvement | |
| cN1 | Evidence of preauricular, submandibular, and cervical lymph node involvement | |
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| cM0 | No signs or symptoms of intracranial or distant metastasis | |
| cM1 | Distant metastasis without microscopic confirmation | |
| cM1a | Tumour(s) involving any distant site (e.g. bone marrow, liver) on clinical or radiological tests | |
| cM1b | Tumour involving the central nervous system on radiological imaging (not including trilateral retinoblastoma) | |
| pM1 | Distant metastasis with microscopic confirmation | |
| pM1a | Histopathological confirmation of tumour at any distant site (e.g. bone marrow, liver, or other) | |
| pM1b | Histopathological confirmation of tumour in the cerebrospinal fluid or CNS parenchyma | |
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| HX | Unknown or insufficient evidence of a constitutional RB1 gene mutation | |
| H0 | Normal RB1 alleles in blood tested with demonstrated high sensitivity assays | |
| H1 | Bilateral retinoblastoma, retinoblastoma with an intracranial CNS midline embryonic tumour (i.e. trilateral retinoblastoma), patient with family history of retinoblastoma, or molecular definition of constitutional RB1 gene mutation | |