| H01692 | |
| H番号 | H01692 |
| 名称 | 上衣下巨細胞性星細胞腫 |
| 概要 | Subependymal giant cell astrocytoma (SEGA) is the most common central nervous system tumor in patients with tuberous sclerosis complex (TSC). Although these lesions are generally benign and non-infiltrative, they commonly arise in the region of the foramen of Monro, where they can cause obstructive hydrocephalus and sudden death. TSC is an autosomal dominant genetic disorder caused by inactivating mutations in either the TSC1 or TSC2 genes. These mutations lead to constitutive upregulation of the mammalian target of rapamycin (mTOR) pathway, which affects many cellular processes involved in tumor growth. Clinical studies have demonstrated that mTOR inhibitors can induce regression of SEGA in patients with TSC, providing a viable alternative to surgical removal. |
| カテゴリ | 神経系疾患 |
| ネットワーク | - |
| 病因遺伝子 | (TSC1) TSC1 [HSA:7248] [KO:K07206] (TSC2) TSC2 [HSA:7249] [KO:K07207] |
| 病原体 | - |
| 環境要因 | - |
| 発癌物質 | - |
| 治療薬 | エベロリムス [DR:D02714] |
| コメント | See also H00915 Tuberous sclerosis complex (TSC) |
| リンク | ICD-11: 2A00.0Y ICD-10: D43.2 MeSH: D001254 |
| 文献 | PMID:24143074 著者 Franz DN タイトル Everolimus in the treatment of subependymal giant cell astrocytomas, angiomyolipomas, and pulmonary and skin lesions associated with tuberous sclerosis complex. 雑誌 Biologics 7:211-21 (2013) DOI:10.2147/BTT.S25095 PMID:32103336 (TSC1 TSC2) 著者 Fohlen M, Harzallah I, Polivka M, Giuliano F, Pons L, Streichenberger N, Dorfmuller G, Touraine R タイトル Identification of TSC1 or TSC2 mutation limited to the tumor in three cases of solitary subependymal giant cell astrocytoma using next-generation sequencing technology. 雑誌 Childs Nerv Syst 36:961-965 (2020) DOI:10.1007/s00381-020-04551-4 |