Chronic neutrophilic leukemia




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Narrow down the case reports



Total: 71 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(50.0%)
26137123
Diagnosis, complications and management of chronic neutrophilic leukaemia: A case report.
Silva PR, Ferreira C, Bizarro S, Cerveira N, Torres L, Moreira I, Mariz JM.
Oncol Lett. 2015;9(6):2657-2660.
Cerebral hemorrhage Splenomegaly Macrocytic anemia
1
(50.0%)
23344408
Pregnancy in a woman with chronic neutrophilic leukemia.
Taylor J, Roboz GJ, Baergen RN, Genc MR.
Obstet Gynecol. 2013;121(2 Pt 2 Suppl 1):457-60.
Splenomegaly Anemia
Abdominal Cavity Adult Anemia Antineoplastic Agents Chronic Neutrophilic Leukemia Females Homo sapiens Infant, Newborn Leukocytosis Platelet Transfusion Postoperative Hemorrhage Pre-Eclampsia Pregnancy Pregnancy Complications, Neoplastic Red Blood Cell Transfusion Repeat Cesarean Section Splenomegaly Thrombocytopenia
1
(50.0%)
7823400
[A case of chronic neutrophilic leukemia accompanied with severe bone marrow fibrosis which was effectively treated by hydroxyurea].
Hirayama Y, Koda K, Matsumoto S, Takayanagi M, Ezoe A, Nobuoka A, Nakazawa O.
Rinsho Ketsueki. 1994;35(11):1329-34.
Splenomegaly Anemia
CSF3
Chronic Neutrophilic Leukemia Homo sapiens Male Middle Aged Primary Myelofibrosis
4
(48.9%)
28205462
Atypical chronic myeloid leukemia in a German Shepherd Dog.
Marino CL, Tran JNSN, Stokol T.
J Vet Diagn Invest. 2017;29(3):338-345.
Anemia Dehydration Vomiting Generalized lymphadenopathy
Animals Blood Cell Count Bone Marrow Canis familiaris Differential Diagnosis Dog Diseases Flow Cytometry Fluorescent in Situ Hybridization Leukemia, Myeloid, Chronic, Atypical, BCR-ABL Nega... Male
5
(48.9%)
7715083
[Association of chronic neutrophilic leukemia and myeloma with fibrillar inclusions in granulocytes].
Mori H, Takahashi N, Tada J, Maeda T, Higuchi T, Shimizu T, Harada H, Miyoshi Y, Okada S, Niikura H, et al..
Rinsho Ketsueki. 1995;36(2):121-7.
Hepatosplenomegaly Anemia
IGHG3
Chronic Neutrophilic Leukemia Females Homo sapiens Inclusion Bodies Middle Aged Multiple Myeloma
6
(45.3%)
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 Splenomegaly Neutrophilia
6
(45.3%)
19652431
Miliary tuberculosis associated with chronic neutrophilic leukemia.
Sugino K, Gocho K, Ota H, Kobayashi M, Sano G, Isobe K, Takai Y, Izumi H, Kuraishi Y, Shibuya K, Homma S.
Intern Med. 2009;48(15):1283-7.
Splenomegaly Fever Leukocytosis
p|SUB|V|617|F;RS#:77375493
Bone Marrow Chronic Neutrophilic Leukemia Females Homo sapiens Homozygote Missense Mutation Spleen Tuberculosis, Miliary Tuberculosis, Splenic X-Ray Computed Tomography
8
(44.2%)
26137042
Concurrent chronic neutrophilic leukemia blast crisis and multiple myeloma: A case report and literature review.
Shi J, Ni Y, Li J, Qiu H, Miao K.
Oncol Lett. 2015;9(5):2208-2210.
Hepatosplenomegaly Leukocytosis Paraproteinemia
ABL1 CSF3
8
(44.2%)
12002774
Coexistence of chronic neutrophilic leukemia with multiple myeloma.
Dincol G, Nalcaci M, Dogan O, Aktan M, Kucukkaya R, Agan M, Dincol K.
Leuk Lymphoma. 2002;43(3):649-51.
Hepatosplenomegaly Leukocytosis Hyperuricemia
Blood Platelets Chronic Neutrophilic Leukemia Fatal Outcome Homo sapiens Immunoglobulin kappa-Chains Male Multiple Myeloma
8
(44.2%)
9352749
Chronic neutrophilic leukemia evolving from a myelodysplastic syndrome.
Pascucci M, Dorion P, Makary A, Froberg MK.
Acta Haematol. 1997;98(3):163-6.
Hepatosplenomegaly Elevated leukocyte alkaline phosphatase Neutrophilia
Chronic Neutrophilic Leukemia Females Homo sapiens Middle Aged
        

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