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DeCS
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Descriptor English:
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Retinoblastoma
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Descriptor Spanish:
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Retinoblastoma
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Descriptor Portuguese:
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Retinoblastoma
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Synonyms English:
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Eye Cancer, Retinoblastoma
Familial Retinoblastoma
Hereditary Retinoblastoma
Sporadic Retinoblastoma
Familial Retinoblastomas
Glioblastomas, Retinal
Gliomas, Retinal
Hereditary Retinoblastomas
Neuroblastomas, Retinal
Retinal Glioblastoma
Retinal Glioblastomas
Retinal Glioma
Retinal Gliomas
Retinal Neuroblastoma
Retinal Neuroblastomas
Retinoblastoma, Familial
Retinoblastoma, Hereditary
Retinoblastoma, Sporadic
Retinoblastomas
Retinoblastomas, Familial
Retinoblastomas, Hereditary
Retinoblastomas, Sporadic
Sporadic Retinoblastomas
Glioblastoma, Retinal
Glioma, Retinal
Neuroblastoma, Retinal
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Tree Number:
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C04.557.465.625.600.725
C04.557.470.670.725
C04.557.580.625.600.725
C04.588.364.818.760
C11.319.475.760
C11.768.717.760
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Definition English:
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A malignant tumor arising from the nuclear layer of the retina that is the most common primary tumor of the eye in children. The tumor tends to occur in early childhood or infancy and may be present at birth. The majority are sporadic, but the condition may be transmitted as an autosomal dominant trait. Histologic features include dense cellularity, small round polygonal cells, and areas of calcification and necrosis. An abnormal pupil reflex (leukokoria); NYSTAGMUS, PATHOLOGIC; STRABISMUS; and visual loss represent common clinical characteristics of this condition. (From DeVita et al., Cancer: Principles and Practice of Oncology, 5th ed, p2104) |
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Indexing Annotation English:
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coordinate IM with RETINAL NEOPLASMS (IM); /genetics: consider also GENES, RETINOBLASTOMA
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See Related English:
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Genes, Retinoblastoma
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Allowable Qualifiers English:
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Record Number:
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12591
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Unique Identifier:
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D012175
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Occurrence in VHL:
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Similar:
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DeCS CID-10 SciELO LILACS LIS
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