Chronic neutrophilic leukemia




Input patient's signs and symptoms


Narrow down the case reports



Total: 71 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(23.3%)
15683121
(4531574)
A case of transition of polycythemia vera to chronic neutrophilic leukemia.
Lee SS, Moon JH, Ha JW, Lee YK, Ahn JS, Zang DY, Kim HJ.
Korean J Intern Med. 2004;19(4):285-8.
Hepatosplenomegaly Low back pain
Aged, 80 and over Chronic Neutrophilic Leukemia Females Homo sapiens Polycythemia Vera
2
(21.2%)
27408367
"Unusual Cause Of Tophi With Renal Thrombotic Microangiopathy".
Sahu KK, Law AD, Kumar G, Dhir V, Naseem S, Nada R, Varma SC, Malhotra P.
Indian J Hematol Blood Transfus. 2016;32(Suppl 1):100-3.
Proteinuria Arthritis
3
(20.4%)
21415944
(3033111)
Monoclonal gammopathy of undetermined significance disguised as chronic neutrophilic leukemia.
Hartley MA, Sokol L, Caceres G, Hussein MA, List A, Pinilla-Ibarz J.
Mediterr J Hematol Infect Dis. 2010;2(1):e2010002.
Hypertension Knee pain
3
(20.4%)
11174417
Leukemia cutis in a patient with chronic neutrophilic leukemia.
Willard RJ, Turiansky GW, Genest GP, Davis BJ, Diehl LF.
J Am Acad Dermatol. 2001;44(2 Suppl):365-9.
Leukemia Bone pain
Antineoplastic Combined Chemotherapy Protocols Bone Marrow Cells Disease Progression Fatal Outcome Females Hand Dermatoses Homo sapiens Leg Dermatoses Skin
3
(20.4%)
8171934
Coexistence of chronic neutrophilic leukemia with light chain myeloma.
Cehreli C, Undar B, Akkoc N, Onvural B, Altungoz O.
Acta Haematol. 1994;91(1):32-4.
Hepatosplenomegaly Bone pain
Antineoplastic Combined Chemotherapy Protocols Biopsy Bone Marrow Chronic Neutrophilic Leukemia Females Homo sapiens Immunoglobulin kappa-Chains Middle Aged Multiple Myeloma Neoplasms, Multiple Primary
6
(4.0%)
31076019
Clonal evolution in a chronic neutrophilic leukemia patient.
Zhang QG, Wang J, Gong WY, Jing QC.
Hematology. 2019;24(1):455-458.
Leukocytosis
c|SUB|C|1853|T;RS#:796065343 c|SUB|G|2373|A p|SUB|T|618|I;RS#:796065343 p|SUB|W|791|*
Chronic Neutrophilic Leukemia Clonal Evolution Homo sapiens Male
6
(4.0%)
30687064
Septic Shock Predisposed by an Underlying Chronic Neutrophilic Leukemia with an Atypical Presentation; A Case Report.
Mendiola VL, Qian YW, Jana B.
Case Rep Oncol. 2018;11(3):871-879.
Splenomegaly
CSF3R FGFR1 JAK2 PCM1 PDGFRA PDGFRB
6
(4.0%)
30473959
(6248686)
Colony-stimulating Factor 3 Receptor Mutated Chronic Neutrophilic Leukemia: A Rare Case Report.
Thapa B, Jamhour C, Chahine J, Rogers HJ, Daw H.
Cureus. 2018;10(9):e3326.
Hepatosplenomegaly
CSF3 CSF3R
6
(4.0%)
29686565
Chronic neutrophilic leukemia.
Bredeweg A, Burch M, Krause JR.
Proc (Bayl Univ Med Cent). 2018;31(1):88-89.
Leukemia
CSF3R
6
(4.0%)
29676020
Chronic neutrophilic leukemia, an extremely rare cause of neutrophilia in childhood: Cure with hematopoietic stem cell transplantation.
Uygun V, Daloglu H, Ozturkmen S, Karasu G, Avc Z, Yesilipek A.
Pediatr Transplant. 2018;22(5):e13199.
Leukopenia
CSF3R
Child Chronic Neutrophilic Leukemia Fanconi Anemia Homo sapiens Male
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 13

HPO ID Term # of case reports
HP:0001974 Leukocytosis 8
HP:0011897 Neutrophilia 7
HP:0001433 Hepatosplenomegaly 5
HP:0001744 Splenomegaly 4
HP:0001909 Leukemia 4
HP:0001873 Thrombocytopenia 2
HP:0031047 Paraproteinemia 2
HP:0001875 Neutropenia 1
HP:0001903 Anemia 1
HP:0011869 Abnormal platelet function 1
HP:0011974 Myelofibrosis 1
HP:0012138 Granulocytic hyperplasia 1
HP:0012311 Monocytosis 1


Causative gene(s) retrieved from Orphanet

    Total: 1

Gene Symbol Gene Name Entrez Gene ID
CSF3R colony stimulating factor 3 receptor 1441