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Acute monocytic leukemia

MedGen UID:
7319
Concept ID:
C0023465
Neoplastic Process
Synonyms: Acute Monoblastic Leukemia; Acute Monoblastic Leukemias; Acute Monocytic Leukemia; Acute Monocytic Leukemias; Leukemia, Acute Monocytic; Leukemia, Monoblastic, Acute; Leukemia, Monocytic, Acute; Leukemia, Myeloid, Acute, M5; Leukemia, Myeloid, Schilling Type; Leukemia, Myeloid, Schilling-Type; Leukemia, Schilling-Type Myeloid; Leukemias, Acute Monoblastic; Leukemias, Acute Monocytic; Monoblastic Leukemia, Acute; Monoblastic Leukemias, Acute; Monocytic Leukemia, Acute; Monocytic Leukemias, Acute; Myeloid Leukemia, Acute, M5; Myeloid Leukemia, Schilling Type; Myeloid Leukemia, Schilling-Type; Schilling-Type Myeloid Leukemia
SNOMED CT: Acute monocytic leukemia (413441006); Acute monocytic leukemia, morphology (22331004); Acute monocytic leukemia (22331004); Acute monoblastic leukemia (22331004); FAB M5 (22331004); FAB M5B (22331004); Acute monoblastic leukemia (413441006)
Modes of inheritance:
Not genetically inherited
MedGen UID:
988794
Concept ID:
CN307044
Finding
Source: Orphanet
clinical entity without genetic inheritance.
 
HPO: HP:0004845
Monarch Initiative: MONDO:0007896
OMIM®: 151380
Orphanet: ORPHA514

Definition

The accumulation of transformed primitive hematopoietic blast cells, which lose their ability of normal differentiation and proliferation. [from HPO]

Clinical features

From HPO
Acute monocytic leukemia
MedGen UID:
7319
Concept ID:
C0023465
Neoplastic Process
The accumulation of transformed primitive hematopoietic blast cells, which lose their ability of normal differentiation and proliferation.

Term Hierarchy

CClinical test,  RResearch test,  OOMIM,  GGeneReviews,  VClinVar  
  • CROGVAcute monocytic leukemia

Conditions with this feature

Acute monocytic leukemia
MedGen UID:
7319
Concept ID:
C0023465
Neoplastic Process
The accumulation of transformed primitive hematopoietic blast cells, which lose their ability of normal differentiation and proliferation.
Hereditary thrombocytopenia and hematological cancer predisposition syndrome associated with RUNX1
MedGen UID:
321945
Concept ID:
C1832388
Disease or Syndrome
RUNX1 familial platelet disorder with associated myeloid malignancies (RUNX1-FPDMM) is characterized by prolonged bleeding and/or easy bruising and an increased risk of developing a hematologic malignancy. RUNX1-FPDMM is characterized by thrombocytopenia with normal platelet size; bleeding is often greater than expected due to qualitative platelet dysfunction. Myeloid malignancies are the most common, including acute myelogenous leukemia (and myelodysplastic syndrome. T- and B-cell acute lymphoblastic leukemias and lymphomas have also been reported, as well as skin manifestations (e.g., eczema, psoriasis).
Neutropenia, severe congenital, 1, autosomal dominant
MedGen UID:
348506
Concept ID:
C1859966
Disease or Syndrome
ELANE-related neutropenia includes congenital neutropenia and cyclic neutropenia, both of which are primary hematologic disorders characterized by recurrent fever, skin and oropharyngeal inflammation (i.e., mouth ulcers, gingivitis, sinusitis, and pharyngitis), and cervical adenopathy. Infectious complications are generally more severe in congenital neutropenia than in cyclic neutropenia. In congenital neutropenia, omphalitis immediately after birth may be the first sign; in untreated children diarrhea, pneumonia, and deep abscesses in the liver, lungs, and subcutaneous tissues are common in the first year of life. After 15 years with granulocyte colony-stimulating factor treatment, the risk of developing myelodysplasia (MDS) or acute myelogenous leukemia (AML) is approximately 15%-25%. Cyclic neutropenia is usually diagnosed within the first year of life based on approximately three-week intervals of fever and oral ulcerations and regular oscillations of blood cell counts. Cellulitis, especially perianal cellulitis, is common during neutropenic periods. Between neutropenic periods, affected individuals are generally healthy. Symptoms improve in adulthood. Cyclic neutropenia is not associated with risk of malignancy or conversion to leukemia.

Professional guidelines

PubMed

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Recent clinical studies

Etiology

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Diagnosis

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Therapy

Beatty CJ, Ghareeb ER
N Engl J Med 2021 Aug 5;385(6):e19. doi: 10.1056/NEJMicm2101571. PMID: 34347955
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Prognosis

Terao T, Matsue K
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Clinical prediction guides

Wang X, Wang Y, Chen J, Wang Q, Liu Z, Yin Y, Yang T, Shen T, Sa Y
Sci Rep 2024 May 2;14(1):10114. doi: 10.1038/s41598-024-60859-0. PMID: 38698063Free PMC Article
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Recent systematic reviews

Fang JF, Yuan HN, Song YF, Sun PB, Zheng XL, Wang XJ
Chin Med J (Engl) 2017 Jun 20;130(12):1481-1490. doi: 10.4103/0366-6999.207474. PMID: 28584213Free PMC Article

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