TERMIUM Plus®
The Government of Canada’s terminology and linguistic data bank.
PANCYTOPENIE [6 records]
Record 1 - internal organization data 2015-11-26
Record 1, English
Record 1, Subject field(s)
- Blood
Record 1, Main entry term, English
- hypersplenism
1, record 1, English, hypersplenism
correct
Record 1, Abbreviations, English
Record 1, Synonyms, English
Record 1, Textual support, English
Record number: 1, Textual support number: 1 DEF
A clinical syndrome in which splenic function becomes excessive as the spleen and its MPS [mononuclear-phagocyte system] tissues enlarge. 1, record 1, English, - hypersplenism
Record number: 1, Textual support number: 1 OBS
It is defined by the following criteria: splenomegaly, a deficiency of at least one or more of the peripheral blood cell lines, normal or increased levels of bone marrow precursors, and an expectation that splenectomy will resolve the cytopenias. 1, record 1, English, - hypersplenism
Record 1, French
Record 1, Domaine(s)
- Sang
Record 1, Main entry term, French
- hypersplénisme
1, record 1, French, hyperspl%C3%A9nisme
correct, masculine noun
Record 1, Abbreviations, French
Record 1, Synonyms, French
Record 1, Textual support, French
Record number: 1, Textual support number: 1 CONT
L'hypersplénisme, défini par l'association d’une pancytopénie(anémie, leucopénie, thrombopénie), d’une splénomégalie et d’une moelle osseuse riche [...] 1, record 1, French, - hyperspl%C3%A9nisme
Record 1, Spanish
Record 1, Textual support, Spanish
Record 2 - internal organization data 2012-02-16
Record 2, English
Record 2, Subject field(s)
- Liver and Biliary Ducts
Record 2, Main entry term, English
- Banti's disease
1, record 2, English, Banti%27s%20disease
correct
Record 2, Abbreviations, English
Record 2, Synonyms, English
- Klemperer's disease 2, record 2, English, Klemperer%27s%20disease
correct
- congestive splenomegaly 2, record 2, English, congestive%20splenomegaly
correct
- splenic anemia 2, record 2, English, splenic%20anemia
correct
Record 2, Textual support, English
Record number: 2, Textual support number: 1 DEF
Originally described as a primary disease of the spleen associated with splenomegaly and pancytopenia, but later considered secondary to portal hypertension. 2, record 2, English, - Banti%27s%20disease
Record 2, French
Record 2, Domaine(s)
- Foie et voies biliaires
Record 2, Main entry term, French
- maladie de Banti
1, record 2, French, maladie%20de%20Banti
correct, feminine noun
Record 2, Abbreviations, French
Record 2, Synonyms, French
- cirrhose splénomégalique 2, record 2, French, cirrhose%20spl%C3%A9nom%C3%A9galique
correct, feminine noun
- anémie de Banti 2, record 2, French, an%C3%A9mie%20de%20Banti
correct, feminine noun
- cirrhose réticulo-endothéliale 2, record 2, French, cirrhose%20r%C3%A9ticulo%2Dendoth%C3%A9liale
feminine noun
- maladie de Bruhl 2, record 2, French, maladie%20de%20Bruhl
feminine noun
Record 2, Textual support, French
Record number: 2, Textual support number: 1 DEF
Affection de la rate associée à une splénomégalie, une pancytopénie périphérique avec moelle riche, et des signes d’hypertension portale avec altération fonctionnelle et anatomique du foie. 2, record 2, French, - maladie%20de%20Banti
Record 2, Spanish
Record 2, Textual support, Spanish
Record 3 - internal organization data 2010-04-13
Record 3, English
Record 3, Subject field(s)
- Genetics
Record 3, Main entry term, English
- Pearson syndrome
1, record 3, English, Pearson%20syndrome
correct
Record 3, Abbreviations, English
Record 3, Synonyms, English
Record 3, Textual support, English
Record number: 3, Textual support number: 1 CONT
McShane MA, Hammans SR, Sweeney M, Holt IJ et al. Pearson syndrome and mitochondrial encephalomyopathy in a patient with a deletion of mtDNA. Am J, Hum Genet 48: 39 (1991) Abstract. 1, record 3, English, - Pearson%20syndrome
Record 3, French
Record 3, Domaine(s)
- Génétique
Record 3, Main entry term, French
- syndrome de Pearson
1, record 3, French, syndrome%20de%20Pearson
correct, masculine noun
Record 3, Abbreviations, French
Record 3, Synonyms, French
Record 3, Textual support, French
Record number: 3, Textual support number: 1 DEF
Pancytopénie de la première enfance avec insuffisance pancréatique. 1, record 3, French, - syndrome%20de%20Pearson
Record 3, Spanish
Record 3, Textual support, Spanish
Record 4 - internal organization data 2010-03-10
Record 4, English
Record 4, Subject field(s)
- Human Diseases - Various
- Genetics
Record 4, Main entry term, English
- Fanconi's syndrome
1, record 4, English, Fanconi%27s%20syndrome
correct
Record 4, Abbreviations, English
Record 4, Synonyms, English
- Fanconi's anemia 2, record 4, English, Fanconi%27s%20anemia
correct
Record 4, Textual support, English
Record number: 4, Textual support number: 1 DEF
A rare recessive disorder with a poor prognosis, characterized by pancytopenia, bone marrow hypoplasia, and patchy brown skin discoloration due to deposition of melanin, as well as multiple congenital anomalies of the musculoskeletal and genitourinary systems. 1, record 4, English, - Fanconi%27s%20syndrome
Record 4, French
Record 4, Domaine(s)
- Maladies humaines diverses
- Génétique
Record 4, Main entry term, French
- maladie de Fanconi
1, record 4, French, maladie%20de%20Fanconi
correct, feminine noun
Record 4, Abbreviations, French
Record 4, Synonyms, French
- anémie de Fanconi 2, record 4, French, an%C3%A9mie%20de%20Fanconi
correct, feminine noun
Record 4, Textual support, French
Record number: 4, Textual support number: 1 DEF
Affection rare, de transmission héréditaire autosomique récessive, dont les symptômes chez les patients homozygotes associent des malformations congénitales du squelette(anomalies hexadactyles), des reins(fusionnés en fer à cheval), la présence de taches pigmentées sur la peau et surtout une pancytopénie progressive, par insuffisance de production de la moelle osseuse apparaissant au cours de la première décennie de la vie. 1, record 4, French, - maladie%20de%20Fanconi
Record 4, Spanish
Record 4, Textual support, Spanish
Record 5 - internal organization data 2009-09-25
Record 5, English
Record 5, Subject field(s)
- Human Diseases - Various
- Blood
Record 5, Main entry term, English
- primary hemophagocytic lymphohistiocytosis
1, record 5, English, primary%20hemophagocytic%20lymphohistiocytosis
correct
Record 5, Abbreviations, English
Record 5, Synonyms, English
- familial hemophagocytic lymphohistiocytosis 2, record 5, English, familial%20hemophagocytic%20lymphohistiocytosis
correct
- FHLH 2, record 5, English, FHLH
correct
- FHLH 2, record 5, English, FHLH
- familial HLH 2, record 5, English, familial%20HLH
correct
- primary HLH 3, record 5, English, primary%20HLH
correct
Record 5, Textual support, English
Record number: 5, Textual support number: 1 CONT
Primary hemophagocytic lymphohistiocytosis [HLH] ... is a heterogeneous autosomal recessive disorder found to be more prevalent with parental consanguinity. [Like secondary hemophagocytic lymphohistiocytosis, it is] characterized by the overwhelming activation of normal T lymphocytes and macrophages, invariably leading to clinical and hematologic alterations and death in the absence of treatment. 1, record 5, English, - primary%20hemophagocytic%20lymphohistiocytosis
Record 5, French
Record 5, Domaine(s)
- Maladies humaines diverses
- Sang
Record 5, Main entry term, French
- lymphohistiocytose hémophagocytaire familiale
1, record 5, French, lymphohistiocytose%20h%C3%A9mophagocytaire%20familiale
correct, feminine noun
Record 5, Abbreviations, French
- LHF 1, record 5, French, LHF
correct, feminine noun
Record 5, Synonyms, French
- lymphohistiocytose hémophagocytaire primitive 2, record 5, French, lymphohistiocytose%20h%C3%A9mophagocytaire%20primitive
correct, feminine noun, less frequent
Record 5, Textual support, French
Record number: 5, Textual support number: 1 CONT
Lymphohistiocytose hémophagocytaire familiale. Cette affection autosomique récessive touche un enfant sur 50 000. Elle se traduit par l'apparition, chez de très jeunes enfants, d’une fièvre associée à une hépatosplénomégalie, une pancytopénie, une hypertriglycéridémie, une hypofibrinogènémie et des troubles neurologiques sévères. La concentration sérique de cytokines pro-inflammatoires [...] est augmentée. Une caractéristique histologique de l'affection est l'accumulation de macrophages et de lymphocytes activés [...], avec images d’hémophagocytose dans la moelle osseuse, la rate, le foie, les ganglions et le système nerveux central. 1, record 5, French, - lymphohistiocytose%20h%C3%A9mophagocytaire%20familiale
Record 5, Spanish
Record 5, Textual support, Spanish
Record 6 - internal organization data 1993-02-25
Record 6, English
Record 6, Subject field(s)
- Blood
- Bones and Joints
Record 6, Main entry term, English
- hypercellular bone marrow
1, record 6, English, hypercellular%20bone%20marrow
correct
Record 6, Abbreviations, English
Record 6, Synonyms, English
Record 6, Textual support, English
Record number: 6, Textual support number: 1 CONT
Pancytopenia with hypercellular bone marrow. A possible paraneoplastic syndrome in carcinoma of the lung. 2, record 6, English, - hypercellular%20bone%20marrow
Record number: 6, Textual support number: 1 OBS
Example extracted from PASCAL data base. 2, record 6, English, - hypercellular%20bone%20marrow
Record 6, French
Record 6, Domaine(s)
- Sang
- Os et articulations
Record 6, Main entry term, French
- moelle osseuse hypercellulaire
1, record 6, French, moelle%20osseuse%20hypercellulaire
correct, feminine noun
Record 6, Abbreviations, French
Record 6, Synonyms, French
Record 6, Textual support, French
Record number: 6, Textual support number: 1 CONT
Un malade avec une pancytopénie et une moelle osseuse hypercellulaire mais sans signes d’hémolyse présente un test de l'antiglobuline directe positif en raison d’un autoanticorps érythrocytaire. 1, record 6, French, - moelle%20osseuse%20hypercellulaire
Record number: 6, Textual support number: 1 OBS
Contexte tiré de la base de données PASCAL. 1, record 6, French, - moelle%20osseuse%20hypercellulaire
Record 6, Spanish
Record 6, Textual support, Spanish
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