Show pageBacklinksCite current pageExport to PDFBack to top This page is read only. You can view the source, but not change it. Ask your administrator if you think this is wrong. ====== Pineal region tumor clinical features ====== {{rss>https://pubmed.ncbi.nlm.nih.gov/rss/search/1PmHMZgOpEG59TdtgSi9LIH6_gI9I3AaJQCGT-zCUuVOHu1EQn/?limit=15&utm_campaign=pubmed-2&fc=20230214022739}} Almost all patients have hydrocephalus by the time of presentation, causing typical signs and symptoms of headache, vomiting, lethargy, memory disturbance, abnormally increasing head circumference in infants, and seizures. [[Parinaud’s syndrome]], or [[sylvian aqueduct syndrome]], may be present. ---- [[Precocious puberty]] may occur only in boys with choriocarcinomas or germinomas with syncytiotrophoblastic cells, due to luteinizing hormone-like effects of β-hCG secreted in the CSF. Suprasellar [[germ cell tumor]]: triad of [[diabetes insipidus]], [[visual deficit]], and [[panhypopituitarism]]. ===== Pineal Region Tumor Hydrocephalus ===== see [[Pineal Region Tumor Hydrocephalus]]. ===== Parinaud syndrome ===== [[Parinaud syndrome]]. ===== Radiculopathy-Myelopathy ===== Drop metastases from CSF seeding can produce [[radiculopathy]] and/or [[myelopathy]]. pineal_region_tumor_clinical_features.txt Last modified: 2024/06/07 02:59by 127.0.0.1