Demyelination due to primary central nervous system lymphoma (Q94708): Difference between revisions
From determinar.ia.br - Determine suas informações
Created a new Item |
Changed an Item |
||||||||||||||
| (6 intermediate revisions by the same user not shown) | |||||||||||||||
| description / pt-br | description / pt-br | ||||||||||||||
Linfoma primário do sistema nervoso central (SNC) é uma forma incomum de linfoma não-Hodgkin (LNH) que tem apresentado aumento da incidência ao longo das últimas três décadas. Diferentemente do linfoma não Hodgkin extranodal sistêmico, a resposta a terapia para linfoma primário do sistema nervoso central tem sido um tanto insatisfatória. Linfoma primário do SNC pode se apresentar como lesão solitária ou lesões multifocais. As lesões multifocais podem ser de vários tamanhos - algumas grandes com efeito de massa e outras menores, e podem ocorrer na substância branca do cérebro. Isso pode se assemelhar a desmielinização. | |||||||||||||||
| description / en | description / en | ||||||||||||||
Primary central nervous system lymphoma is an uncommon form of non-Hodgkin's lymphoma (NHL) that has been increasing in incidence over the past three decades. Unlike systemic extranodal non-Hodgkin's lymphoma, the response to therapy for primary central nervous system lymphoma patients has been somewhat unsatisfactory. Primary CNS lymphoma may present as solitary or multifocal lesions. The multifocal lesions can be of various size-some large with mass effect and others smaller, and can occur in the cerebral white matter. This can resemble demyelination. | |||||||||||||||
| Property / Canonical URI | |||||||||||||||
| Property / Canonical URI: https://id.who.int/icd/entity/2062450262 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / CURIE | |||||||||||||||
CID11:ID_2062450262 | |||||||||||||||
| Property / CURIE: CID11:ID_2062450262 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Canary Token | |||||||||||||||
dki-india-ID_2062450262 | |||||||||||||||
| Property / Canary Token: dki-india-ID_2062450262 / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Verification Status | |||||||||||||||
Concluído | |||||||||||||||
| Property / Verification Status: Concluído / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Knowledge Architect | |||||||||||||||
| Property / Knowledge Architect: https://pauloleads.com.br/cases-publicos/ / rank | |||||||||||||||
Normal rank | |||||||||||||||
| Property / Collection date | |||||||||||||||
15 August 2026
| |||||||||||||||
| Property / Collection date: 15 August 2026 / rank | |||||||||||||||
Normal rank | |||||||||||||||
Latest revision as of 10:06, 16 August 2026
Primary central nervous system lymphoma is an uncommon form of non-Hodgkin's lymphoma (NHL) that has been increasing in incidence over the past three decades. Unlike systemic extranodal non-Hodgkin's lymphoma, the response to therapy for primary central nervous system lymphoma patients has been somewhat unsatisfactory. Primary CNS lymphoma may present as solitary or multifocal lesions. The multifocal lesions can be of various size-some large with mass effect and others smaller, and can occur in the cerebral white matter. This can resemble demyelination.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | ID_2062450262 |
||
| English | Demyelination due to primary central nervous system lymphoma |
Primary central nervous system lymphoma is an uncommon form of non-Hodgkin's lymphoma (NHL) that has been increasing in incidence over the past three decades. Unlike systemic extranodal non-Hodgkin's lymphoma, the response to therapy for primary central nervous system lymphoma patients has been somewhat unsatisfactory. Primary CNS lymphoma may present as solitary or multifocal lesions. The multifocal lesions can be of various size-some large with mass effect and others smaller, and can occur in the cerebral white matter. This can resemble demyelination. |
Statements
CID11:ID_2062450262
0 references
dki-india-ID_2062450262
0 references
Concluído
0 references
15 August 2026
0 references
