Choroid plexus carcinoma: a rare condition and its therapeutic management
Choroid plexus carcinomas are rare tumours, found chiefly during childhood. The commonest pattern of progression is via the neural axis. We present the case of a patient with unusual metastatic dissemination, affecting lungs and bones two years after diagnosis, and the approach adopted towards him.
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| Veröffentlicht in: | Clinical & translational oncology 2007-06, Vol.9 (6), p.401-403 |
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| container_issue | 6 |
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| container_title | Clinical & translational oncology |
| container_volume | 9 |
| creator | Fernández Calvo, O Gallegos Sancho, Maria I Quindós Varela, M Paredes Velázquez, L Dopico Vázquez, D Antón Aparicio, L M |
| description | Choroid plexus carcinomas are rare tumours, found chiefly during childhood. The commonest pattern of progression is via the neural axis. We present the case of a patient with unusual metastatic dissemination, affecting lungs and bones two years after diagnosis, and the approach adopted towards him. |
| doi_str_mv | 10.1007/s12094-007-0073-9 |
| format | Article |
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| fulltext | fulltext |
| identifier | ISSN: 1699-048X |
| ispartof | Clinical & translational oncology, 2007-06, Vol.9 (6), p.401-403 |
| issn | 1699-048X 1699-3055 |
| language | eng |
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| source | MEDLINE; Springer Online Journals Complete |
| subjects | Adult Bone Neoplasms - secondary Carcinoma - secondary Carcinoma - therapy Choroid Plexus Neoplasms - pathology Choroid Plexus Neoplasms - therapy Humans Lung Neoplasms - secondary Male |
| title | Choroid plexus carcinoma: a rare condition and its therapeutic management |
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