Chronic neutrophilic leukaemia (Q39441): Difference between revisions
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Neoplasia mieloproliferativa crônica rara caracterizada por neutrofilia persistente no sangue periférico, hipercelularidade da medula óssea devida a proliferação de granulócitos neutrofílicos e hepatoesplenomegalia. Os neutrófilos não têm displasia e frequentemente apresentam granulações tóxicas. Não há cromossomo Filadélfia ou gene de fusão BCR-ABL1 detectável. | |||
| description / en | description / en | ||
A rare chronic myeloproliferative neoplasm characterised by sustained peripheral blood neutrophilia, bone marrow hypercellularity due to neutrophilic granulocyte proliferation, and hepatosplenomegaly. The neutrophils lack dysplasia and often show toxic granulations. There is no detectable Philadelphia chromosome or BCR/ABL1 fusion gene. | |||
Revision as of 04:51, 13 August 2026
A rare chronic myeloproliferative neoplasm characterised by sustained peripheral blood neutrophilia, bone marrow hypercellularity due to neutrophilic granulocyte proliferation, and hepatosplenomegaly. The neutrophils lack dysplasia and often show toxic granulations. There is no detectable Philadelphia chromosome or BCR/ABL1 fusion gene.
| Language | Label | Description | Also known as |
|---|---|---|---|
| default for all languages | 2A20.1 |
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| English | Chronic neutrophilic leukaemia |
A rare chronic myeloproliferative neoplasm characterised by sustained peripheral blood neutrophilia, bone marrow hypercellularity due to neutrophilic granulocyte proliferation, and hepatosplenomegaly. The neutrophils lack dysplasia and often show toxic granulations. There is no detectable Philadelphia chromosome or BCR/ABL1 fusion gene. |
