Acute panmyelosis with myelofibrosis




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Narrow down the case reports



Total: 63 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
1
(61.3%)
2593246
[Acute myelofibrosis terminating in acute myelomegakaryoblastic leukemia].
Shiozaki H, Iwahashi C, Suzuki T, Miyoshi K, Kurane R, Yamato K, Enomoto Y.
Rinsho Ketsueki. 1989;30(10):1806-9.
Hepatosplenomegaly Fever Poikilocytosis
ANPEP CYTL1
Acute Disease Acute Megakaryocytic Leukemias Adult Females Homo sapiens Leukemia, Myelocytic, Acute Primary Myelofibrosis
2
(56.2%)
15125608
Fatal familial infantile myelofibrosis.
Sheikha A.
J Pediatr Hematol Oncol. 2004;26(3):164-8.
Splenomegaly Anisopoikilocytosis
Acute Megakaryocytic Leukemias Adult Fatal Outcome Females Homo sapiens Infant Male Primary Myelofibrosis
2
(56.2%)
6576466
[Acute osteomyelofibrosis. An overview and 2 personal cases].
Strebel U, Schaffner A, Fehr J.
Schweiz Med Wochenschr. 1983;113(23):844-50.
Splenomegaly Poikilocytosis
Adult Differential Diagnosis Females Hairy Cell Leukemia Homo sapiens Male Middle Aged Myeloid Leukemia Primary Myelofibrosis
2
(56.2%)
2496279
[Acute myelofibrosis: apropos of a case with immunocytochemical and ultrastructural studies].
Ocana I, Alegre J, Fernandez de Sevilla T, Ruiz Marcellan L, Ribera E, Martinez Vazquez JM.
Med Clin (Barc). 1989;92(3):102-3.
Splenomegaly Anisopoikilocytosis
COX8A
Biopsy Differential Diagnosis Electron Microscopy Homo sapiens Immunoenzyme Techniques Male Megakaryocytes Primary Myelofibrosis
2
(56.2%)
851094
Acute myelofibrosis: a report of three cases.
Fabich DR, Raich PC.
Am J Clin Pathol. 1977;67(4):334-8.
Splenomegaly Poikilocytosis
Acute Disease Blood Cells Bone Marrow Bone Marrow Cells Homo sapiens Male Middle Aged Pancytopenia Primary Myelofibrosis
2
(56.2%)
367569
Acute ("malignant") myelosclerosis.
Bearman RM, Pangalis GA, Rappaport H.
Cancer. 1979;43(1):279-93.
Splenomegaly Poikilocytosis
Acute Disease Adult Bone Marrow Erythroblasts Females Homo sapiens Male Megakaryocytes Middle Aged Primary Myelofibrosis Spleen Terminology as Topic
7
(55.7%)
318917
Idiopathic acquired sideroblastic anemia terminating in acute myelofibrosis: case report and review of leterature.
Yeung K, Trowbridge AA.
Cancer. 1977;39(1):359-65.
Hepatosplenomegaly Anemia Poikilocytosis
Acute Disease Adult Bone Marrow Females Fibroblasts Homo sapiens Male Middle Aged Primary Myelofibrosis
8
(50.0%)
21274282
(3026984)
Successful control of acute myelofibrosis with lenalidomide.
Vassilopoulos G, Palassopoulou M, Zisaki K, Befani M, Bouronikou E, Giannakoulas N, Stathopoulou E, Matsouka P.
Case Rep Med. 2010;2010:421239.
Splenomegaly Anemia
8
(50.0%)
119413
Acute agnogenic myeloid metaplasia with chromosomal abnormalities.
Bartoli E, Massarelli G, Soggia G, Tanda F, Vianello MG.
Acta Haematol. 1979;62(4):206-13.
Splenomegaly Anemia
Acute Disease Adult Bone Marrow Chromosomes, Human, 6-12 and X Females Hematopoiesis Homo sapiens Leukopenia Primary Myelofibrosis Splenomegaly Trisomy
10
(48.9%)
14565665
Acute myelofibrosis in a patient with diffuse large cell non Hodgkin's lymphoma and renal cancer.
Mohren M, Essbach U, Franke A, Klink A, Maas C, Markmann I, Pelz AF, Jentsch-Ullrich K.
Leuk Lymphoma. 2003;44(9):1603-7.
Hepatosplenomegaly Anemia
Antineoplastic Combined Chemotherapy Protocols Bone Marrow Chromosome Aberrations Chromosomes, Human, Pair 2 Chromosomes, Human, Pair 7 Clone Cells Combined Modality Therapy Diffuse Large B-Cell Lymphoma Fatal Outcome Females Genetic Predisposition to Disease Homo sapiens Kidney Neoplasm Middle Aged Neoplasms, Multiple Primary Nephrectomy Pancytopenia Primary Myelofibrosis Renal Cell Carcinoma Ring Chromosomes
        

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