Myeloid sarcoma

Myeloid sarcoma is a rare solid tumor of the myelogenous cells occurring in an extramedullary site.



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Total: 702 (papers)

  


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Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
561
(5.0%)
1395391
Case report: granulocytic sarcoma (chloroma) presenting as a cerebellopontine angle mass.
Romaniuk CS.
Clin Radiol. 1992;45(4):284-5.
Unilateral facial palsy
Cerebellar Neoplasms Child, Preschool Females Homo sapiens Myeloid Leukemia X-Ray Computed Tomography
561
(5.0%)
1057829
[Granulocytic sarcoma of the breast in chronic granulocytic leukemia (author's transl)].
Machacek E.
Zentralbl Allg Pathol. 1975;119(3):175-8.
Amenorrhea
Amenorrhea Females Homo sapiens Menstruation Disturbances Middle Aged Myeloid Leukemia Sarcoma
        

Phenotype(s) retrieved from Orphanet

    Total: 0

HPO ID Term Frequency


Phenotype(s) retrieved from case reports

    Total: 114

HPO ID Term # of case reports
HP:0001909 Leukemia 159
HP:0002488 Acute leukemia 29
HP:0002664 Neoplasm 26
HP:0002835 Aspiration 15
HP:0012324 Myeloid leukemia 13
HP:0100242 Sarcoma 13
HP:0002176 Spinal cord compression 12
HP:0011974 Myelofibrosis 10
HP:0000520 Proptosis 9
HP:0030731 Carcinoma 8
HP:0000952 Jaundice 7
HP:0032061 Hypereosinophilia 7
HP:0002027 Abdominal pain 5
HP:0010550 Paraplegia 5
HP:0001880 Eosinophilia 4
HP:0002202 Pleural effusion 4
HP:0002716 Lymphadenopathy 4
HP:0002861 Melanoma 4
HP:0003419 Low back pain 4
HP:0005558 Chronic leukemia 4
HP:0031501 Pelvic mass 4
HP:0032408 Breast lump 4
HP:0001289 Confusion 3
HP:0001945 Fever 3
HP:0001978 Extramedullary hematopoiesis 3
HP:0002576 Intussusception 3
HP:0003470 Paralysis 3
HP:0007209 Facial paralysis 3
HP:0009792 Teratoma 3
HP:0025615 Abscess 3
HP:0032404 Testicular mass 3
HP:0000508 Ptosis 2
HP:0001342 Cerebral hemorrhage 2
HP:0001369 Arthritis 2
HP:0001482 Subcutaneous nodule 2
HP:0001698 Pericardial effusion 2
HP:0001875 Neutropenia 2
HP:0001903 Anemia 2
HP:0002573 Hematochezia 2
HP:0002721 Immunodeficiency 2
HP:0002863 Myelodysplasia 2
HP:0003002 Breast carcinoma 2
HP:0005214 Intestinal obstruction 2
HP:0005521 Disseminated intravascular coagulation 2
HP:0030838 Hip pain 2
HP:0031500 Abdominal mass 2
HP:0000016 Urinary retention 1
HP:0000112 Nephropathy 1
HP:0000131 Uterine leiomyoma 1
HP:0000246 Sinusitis 1
HP:0000265 Mastoiditis 1
HP:0000421 Epistaxis 1
HP:0000579 Nasolacrimal duct obstruction 1
HP:0000939 Osteoporosis 1
HP:0001028 Hemangioma 1
HP:0001081 Cholelithiasis 1
HP:0001082 Cholecystitis 1
HP:0001217 Clubbing 1
HP:0001269 Hemiparesis 1
HP:0001297 Stroke 1
HP:0001370 Rheumatoid arthritis 1
HP:0001396 Cholestasis 1
HP:0001433 Hepatosplenomegaly 1
HP:0001541 Ascites 1
HP:0001708 Right ventricular failure 1
HP:0001741 Phimosis 1
HP:0001744 Splenomegaly 1
HP:0001824 Weight loss 1
HP:0001873 Thrombocytopenia 1
HP:0001891 Iron deficiency anemia 1
HP:0002014 Diarrhea 1
HP:0002090 Pneumonia 1
HP:0002105 Hemoptysis 1
HP:0002113 Pulmonary infiltrates 1
HP:0002170 Intracranial hemorrhage 1
HP:0002301 Hemiplegia 1
HP:0002385 Paraparesis 1
HP:0002586 Peritonitis 1
HP:0002653 Bone pain 1
HP:0002756 Pathologic fracture 1
HP:0002777 Tracheal stenosis 1
HP:0002797 Osteolysis 1
HP:0002878 Respiratory failure 1
HP:0003764 Nevus 1
HP:0004377 Hematological neoplasm 1
HP:0005240 Esophageal obstruction 1
HP:0005523 Lymphoproliferative disorder 1
HP:0006000 Ureteral obstruction 1
HP:0006515 Interstitial pneumonitis 1
HP:0009789 Perianal abscess 1
HP:0009926 Epiphora 1
HP:0011868 Sciatica 1
HP:0011946 Bronchiolitis obliterans 1
HP:0012056 Cutaneous melanoma 1
HP:0012133 Erythroid hypoplasia 1
HP:0012315 Histiocytoma 1
HP:0012390 Anal fissure 1
HP:0012740 Papilloma 1
HP:0012799 Unilateral facial palsy 1
HP:0025027 Osteoma cutis 1
HP:0025143 Chills 1
HP:0030065 Primitive neuroectodermal tumor 1
HP:0030741 Mediastinal teratoma 1
HP:0031273 Shock 1
HP:0031456 Ectopic pregnancy 1
HP:0032252 Granuloma 1
HP:0100008 Schwannoma 1
HP:0100608 Metrorrhagia 1
HP:0100614 Myositis 1
HP:0100658 Cellulitis 1
HP:0100699 Scarring 1
HP:0100727 Histiocytosis 1
HP:0200023 Priapism 1
HP:0200036 Skin nodule 1


Causative gene(s) retrieved from Orphanet

    Total: 0

Gene Symbol Gene Name Entrez Gene ID