myelomonocytic leukemia


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Related to myelomonocytic leukemia: acute myelomonocytic leukemia

myelomonocytic leukemia

[¦mī·ə·lō‚män·ə¦sid·ik lü′kē·mē·ə]
(medicine)
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References in periodicals archive ?
Takedas presentations will highlight the companys investigations into the epidemiology, prognosis and patient reported outcomes for higher-risk myelodysplastic syndromes (HR-MDS) and the related conditions chronic myelomonocytic leukemia (CMML) and acute myeloid leukemia (AML) to achieve a deep understanding of these rare cancers and the needs of this patient community.
Trisomy/ tetrasomy of chromosome 8 and +i(8q) as the sole chromosome abnormality in three adult patients with myelomonocytic leukemia. Cancer Genet Cytogenet 2000;120:163-165.
Molecular and prognostic correlates of cytogenetic abnormalities in chronic myelomonocytic leukemia: a Mayo Clinic-French Consortium Study.
This category includes myeloid neoplasms with germline GATA2 mutation, bone marrow failure syndromes, telomere biology disorders, Down syndrome or juvenile myelomonocytic leukemia associated with neurofibromatosis, and Noonan syndrome or Noonan syndrome-like disorders.
Acute (ii) All 6 blood culture myelomonocytic leukemia. bottles were flagged WBC count = 150 x positive: at 18 hours [10.sup.9]/L (95% (aerobic, BACTEC NR370), blasts).
Chronic myelomonocytic leukemia (CMML) is a clonal disorder of hematopoietic stem cells (HSCs) that is characterized by the presence of peripheral blood (PB) monocytosis with overlapping features between MDS and myeloproliferative neoplasm (MPN) and a risk of transformation to AML [18, 19].
Despite a lack of neurological symptoms, a lumbar puncture was performed as he was deemed high risk for central nervous system (CNS) involvement due concern for acute myelomonocytic leukemia (AMML).
MS can appear with blast phase/transformation of a myeloproliferative neoplasm, also known as chronic myelomonocytic leukemia. MS may also be associated with a normal bone marrow biopsy and blood smear, without a history of myeloid neoplasia [7-9].
PTPN11 pathogenic variants have been found in approximately 50% cases with NS and are also frequently positively associated with familial inheritance, pulmonary stenosis, ASD, HCM, short stature, sternal deformity, bleeding diathesis, juvenile myelomonocytic leukemia (JMML), and NS/MPD [3, 6, 10].
His blood film showed marked monocytosis, promonocytes, and some circulating blasts suggesting acute myelomonocytic leukemia (AMML) or chronic myelomonocytic leukemia (CMML) in transformation.
The results suggested that changes in the genetic code (mutations) that reduce TET2 function are found in 10 percent of patients with acute myeloid leukemia (AML), 30 percent of those with a form of pre-leukemia called myelodysplastic syndrome, and in nearly 50 percent of patients with chronic myelomonocytic leukemia.
Juvenile myelomonocytic leukemia is characterised by what?