Ha seleccionado la visión en Inglés
Descriptor en español: |
Retinoblastoma
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Descriptor en inglés: | Retinoblastoma | ||||||
Descriptor en portugués: | Retinoblastoma | ||||||
Descriptor en francés: | Rétinoblastome | ||||||
Término(s) alternativo(s): |
Cancer, Retinoblastoma Eye Cancers, Retinoblastoma Eye Eye Cancer, Retinoblastoma Eye Cancers, Retinoblastoma Familial Retinoblastoma Familial Retinoblastomas Glioblastoma, Retinal Glioblastomas, Retinal Glioma, Retinal Gliomas, Retinal Hereditary Retinoblastoma Hereditary Retinoblastomas Neuroblastoma, Retinal Neuroblastomas, Retinal Retinal Glioblastoma Retinal Glioblastomas Retinal Glioma Retinal Gliomas Retinal Neuroblastoma Retinal Neuroblastomas Retinoblastoma Eye Cancer Retinoblastoma Eye Cancers Retinoblastoma, Familial Retinoblastoma, Hereditary Retinoblastoma, Sporadic Retinoblastomas Retinoblastomas, Familial Retinoblastomas, Hereditary Retinoblastomas, Sporadic Sporadic Retinoblastoma Sporadic Retinoblastomas |
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Código(s) jeráquico(s): |
C04.557.465.625.600.725 C04.557.470.670.725 C04.557.580.625.600.725 C04.588.364.818.760 C11.270.862 C11.319.475.760 C11.768.717.760 |
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Identificador Único RDF: | https://id.nlm.nih.gov/mesh/D012175 | ||||||
Nota de alcance: | 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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Nota de indización: | coordinate IM with RETINAL NEOPLASMS (IM); /genetics: consider also GENES, RETINOBLASTOMA |
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Calificadores permitidos: |
BL blood BS blood supply CF cerebrospinal fluid CH chemistry CI chemically induced CL classification CN congenital CO complications DG diagnostic imaging DH diet therapy DI diagnosis DT drug therapy EC economics EH ethnology EM embryology EN enzymology EP epidemiology ET etiology GE genetics HI history IM immunology ME metabolism MI microbiology MO mortality NU nursing PA pathology PC prevention & control PP physiopathology PS parasitology PX psychology RH rehabilitation RT radiotherapy SC secondary SU surgery TH therapy UL ultrastructure UR urine VE veterinary VI virology |
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Vea también los descriptores: |
Genes, Retinoblastoma
MeSH | ||||||
Identificador de DeCS: | 12591 | ||||||
ID del Descriptor: | D012175 | ||||||
Clasificación de la NLM: | WW 270 | ||||||
Documentos indizados en la Biblioteca Virtual de Salud (BVS): | Haga clic aquí para acceder a los documentos de la BVS | ||||||
Fecha de establecimiento: | 01/01/1966 | ||||||
Fecha de entrada: | 01/01/1999 | ||||||
Fecha de revisión: | 15/06/2018 |
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DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Neoplasms [C04]Neoplasms -
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases -
DISEASES
Eye Diseases [C11]Eye Diseases
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Retinoblastoma
- Concepto preferido
Sporadic Retinoblastoma
- Más estrecho
Familial Retinoblastoma
- Más estrecho
UI del concepto |
M0018961 |
Nota de alcance | 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) |
Término preferido | Retinoblastoma |
Término(s) alternativo(s) |
Cancer, Retinoblastoma Eye Cancers, Retinoblastoma Eye Eye Cancer, Retinoblastoma Eye Cancers, Retinoblastoma Glioblastoma, Retinal Glioblastomas, Retinal Glioma, Retinal Gliomas, Retinal Neuroblastoma, Retinal Neuroblastomas, Retinal Retinal Glioblastoma Retinal Glioblastomas Retinal Glioma Retinal Gliomas Retinal Neuroblastoma Retinal Neuroblastomas Retinoblastoma Eye Cancer Retinoblastoma Eye Cancers Retinoblastomas |
UI del concepto |
M0336986 |
Término preferido | Sporadic Retinoblastoma |
Término(s) alternativo(s) |
Retinoblastoma, Sporadic Retinoblastomas, Sporadic Sporadic Retinoblastomas |
UI del concepto |
M0336985 |
Término preferido | Familial Retinoblastoma |
Término(s) alternativo(s) |
Familial Retinoblastomas Hereditary Retinoblastoma Hereditary Retinoblastomas Retinoblastoma, Familial Retinoblastoma, Hereditary Retinoblastomas, Familial Retinoblastomas, Hereditary |
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