Acute panmyelosis with myelofibrosis




Input patient's signs and symptoms


Narrow down the case reports



Total: 63 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
20
(31.4%)
6951405
Acute myelofibrosis.
Rupani M.
Am J Clin Pathol. 1982;77(4):475-8.
Leukopenia Anemia
Acute Disease Adult Bone Marrow Differential Diagnosis Homo sapiens Leukemia, Myelocytic, Acute Male Megakaryocytes Primary Myelofibrosis
22
(27.8%)
24282446
(3837489)
A case of chronic myeloid leukaemia presenting as megakaryocytic blast crisis (AML M7).
Karkuzhali P, Shanthi V, Usha T.
Ecancermedicalscience. 2013;7:375.
Splenomegaly
23
(27.2%)
2963171
Acute myelofibrosis in megakaryoblastic leukemia with translocation between chromosomes 8 and 14.
Winkelmann M, Aul C, Scharf RE, Schmitt-Graff A, Carbonell F, Villeval JL, Grosse-Wilde H, Fischer JT, Schneider W.
Klin Wochenschr. 1987;65(21):1034-41.
Normochromic anemia
Acute Megakaryocytic Leukemias Blood Platelets Bone Marrow Chromosomes, Human, Pair 14 Chromosomes, Human, Pair 8 Electron Microscopy Females Flow Cytometry Homo sapiens Middle Aged Platelet Factor 4 Primary Myelofibrosis beta-Thromboglobulin
24
(20.5%)
23694793
Acute myelofibrosis and acute lymphoblastic leukemia in an elderly patient with previously treated multiple myeloma.
Gonzalez MM, Kidd L, Quesada J, Nguyen N, Chen L.
Ann Clin Lab Sci. 2013;43(2):176-80.
Pancytopenia Leukemia
Blood Cell Count Bone Marrow Homo sapiens Immunohistochemistry Maintenance Chemotherapy Male Multiple Myeloma Precursor Cell Lymphoblastic Leukemia Lymphoma Primary Myelofibrosis
24
(20.5%)
8780742
A case of acute myelofibrosis with complex karyotypic changes: a type of myelodysplastic syndrome.
Allen EF, Lunde JH, McNally R, Branda RE.
Cancer Genet Cytogenet. 1996;90(1):24-8.
Pancytopenia Monocytosis
Acute Disease Bone Marrow Chromosome Aberrations Fatal Outcome Females Homo sapiens Primary Myelofibrosis
24
(20.5%)
8614887
Chronic myeloid leukemia manifested during megakaryoblastic crisis.
Wu CD, Medeiros LJ, Miranda RN, Mark HF, Rintels P.
South Med J. 1996;89(4):422-7.
Pancytopenia Leukocytosis
Acute Megakaryocytic Leukemias Adult Antimetabolites, Antineoplastic Blast Phase Bone Marrow Bone Marrow Transplantation Fatal Outcome Homo sapiens Male
24
(20.5%)
8571944
Acute myelofibrosis terminating in acute lymphoblastic leukemia: case report and review of the literature.
Dunphy CH, Kitchen S, Saravia O, Velasquez WS.
Am J Hematol. 1996;51(1):85-9.
Acute leukemia
Adult Antineoplastic Combined Chemotherapy Protocols Blast Phase Bone Marrow Chromosome Deletion Chromosomes, Human, Pair 5 Combined Modality Therapy Cranial Irradiation Disease Progression Flow Cytometry Homo sapiens Immunophenotyping Male Neoplastic Stem Cells Precursor B-Cell Lymphoblastic Leukemia-Lymphoma Precursor Cell Lymphoblastic Leukemia Lymphoma Primary Myelofibrosis Remission Induction
24
(20.5%)
7573123
Cytogenetic and molecular analysis of a ring (21) in a patient with partial trisomy 21 and megakaryocytic leukemia.
Palmer CG, Blouin JL, Bull MJ, Breitfeld P, Vance GH, Van Meter T, Weaver DD, Heerema NA, Colbern SG, Korenberg JR, et al..
Am J Med Genet. 1995;57(4):527-36.
Leukemia
RUNX1
Acute Megakaryocytic Leukemias Chromosome Mapping Chromosomes, Human, Pair 21 Females Fluorescent in Situ Hybridization Genetic Polymorphism Homo sapiens Infant Ring Chromosomes Trisomy
24
(20.5%)
6928079
Acute myelofibrosis terminating as acute myeloblastic leukemia.
Weisenburger DD.
Am J Clin Pathol. 1980;73(1):128-32.
Leukemia
Antineoplastic Agents Bone Marrow Child Combination Drug Therapy Differential Diagnosis Females Homo sapiens Leukemia, Myelocytic, Acute Primary Myelofibrosis Time Factors
24
(20.5%)
6744217
Myeloproliferative disease in two young siblings.
Cervantes F, Ribera JM, Sanchez-Bisono J, Brugues R, Rozman C.
Cancer. 1984;54(5):899-902.
Pancytopenia Pneumonia
Acute Disease Bone Marrow Child Females HLA Antigens Homo sapiens Liver Male Primary Myelofibrosis
        

Phenotype(s) retrieved from Orphanet

    Total: 15

HPO ID Term Frequency
HP:0001876 Pancytopenia Very frequent (99-80%)
HP:0011974 Myelofibrosis Very frequent (99-80%)
HP:0001324 Muscle weakness Frequent (79-30%)
HP:0012129 Abnormality of bone marrow stromal cells Frequent (79-30%)
HP:0012143 Abnormal megakaryocyte morphology Frequent (79-30%)
HP:0012378 Fatigue Frequent (79-30%)
HP:0031020 Bone marrow hypercellularity Frequent (79-30%)
HP:0003419 Low back pain Occasional (29-5%)
HP:0004808 Acute myeloid leukemia Occasional (29-5%)
HP:0004820 Acute myelomonocytic leukemia Occasional (29-5%)
HP:0005528 Bone marrow hypocellularity Occasional (29-5%)
HP:0031385 Megakaryocyte nucleus hypolobulation Occasional (29-5%)
HP:0031386 Increased micromegakaryocyte count Occasional (29-5%)
HP:0100827 Lymphocytosis Occasional (29-5%)
HP:0001744 Splenomegaly Very rare (4-1%)


Phenotype(s) retrieved from case reports

    Total: 17

HPO ID Term # of case reports
HP:0001909 Leukemia 11
HP:0001876 Pancytopenia 7
HP:0011974 Myelofibrosis 7
HP:0001433 Hepatosplenomegaly 2
HP:0001744 Splenomegaly 2
HP:0002488 Acute leukemia 2
HP:0001894 Thrombocytosis 1
HP:0001903 Anemia 1
HP:0001974 Leukocytosis 1
HP:0002090 Pneumonia 1
HP:0002653 Bone pain 1
HP:0002863 Myelodysplasia 1
HP:0003072 Hypercalcemia 1
HP:0004377 Hematological neoplasm 1
HP:0004447 Poikilocytosis 1
HP:0004823 Anisopoikilocytosis 1
HP:0200036 Skin nodule 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID