Acute panmyelosis with myelofibrosis




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Narrow down the case reports



Total: 63 (papers)

   


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)		 PMID
(PMCID)
61
(11.2%)		 842561
 Acute myelofibrosis and malignant hypercalcemia.
Libnoch JA, Ajlouni K, Millman WL, Guansing AR, Theil GB.
Am J Med. 1977;62(3):432-8.
Hypocalcemia
PTH
Acute Disease Adult Bone Marrow Bone Marrow Cells Bone Marrow Examination Homo sapiens Hypercalcemia Male Primary Myelofibrosis
62
(5.0%)		 9442954
 Acute myelofibrosis mimicking multiple bone metastases on Tc-99m MDP bone imaging.
Oyen WJ, Raemaekers JM, Corstens FH.
Clin Nucl Med. 1998;23(1):1-2.
Neoplasm
Acute Disease Adrenal Cortex Hormones Antineoplastic Agents Biopsy Differential Diagnosis Fatal Outcome Homo sapiens Interferon alpha 2 Interferon-alpha Male Middle Aged Primary Myelofibrosis Radionuclide Imaging Radiopharmaceuticals Recombinant Proteins
62
(5.0%)		 2738653
 Acute myelofibrosis: correlation of radiographic, bone scan, and biopsy findings.
Marino GG, Robinson WL.
J Nucl Med. 1989;30(2):251-4.
Bone pain
Acute Disease Adult Homo sapiens Male Primary Myelofibrosis Radionuclide Imaging
        

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