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)
1
(50.0%)
11737254
Granulocytic sarcoma of megakaryoblastic differentiation in the lymph nodes terminating as acute megakaryoblastic leukemia in a case of chronic idiopathic myelofibrosis persisting for 16 years.
Hirose Y, Masaki Y, Shimoyama K, Sugai S, Nojima T.
Eur J Haematol. 2001;67(3):194-8.
Splenomegaly Anemia
ITGA2B
Acute Megakaryocytic Leukemias Females Homo sapiens Megakaryocytes Middle Aged Neoplastic Cell Transformation Primary Myelofibrosis Sarcoma, Myeloid
2
(44.2%)
28121748
Disseminated Nonleukemic Myeloid Sarcoma of the Spleen With Involvement of the Liver in an Infant.
Rao Y, Wu Y, Dong A, Zhu K, Li W, Cai S, Yang M, Yan J.
J Pediatr Hematol Oncol. 2017;39(4):e233-e235.
Hepatosplenomegaly Fever Hematochezia
Biopsy Differential Diagnosis Fatal Outcome Hepatomegaly Homo sapiens Immunophenotyping Infant Male Sarcoma, Myeloid Splenic Neoplasms Splenomegaly
2
(44.2%)
19656707
Disseminated Mycobacterium kansasii infection associated with hemophagocytic syndrome.
Chou YH, Hsu MS, Sheng WH, Chang SC.
Int J Infect Dis. 2010;14(3):e262-4.
Hepatosplenomegaly Pancytopenia Fever
Females Homo sapiens Lymphohistiocytosis, Hemophagocytic Middle Aged Mycobacterium Infections, Nontuberculous Mycobacterium kansasii
2
(44.2%)
17189221
Multiple granulocytic sarcomas in essential thrombocythemia.
Tanaka Y, Nagai Y, Mori M, Fujita H, Togami K, Kurata M, Matsushita A, Maeda A, Nagai K, Tanaka K, Takahashi T.
Int J Hematol. 2006;84(5):413-6.
Hepatosplenomegaly Leukemia Fever
Antineoplastic Combined Chemotherapy Protocols Blood Transfusion Chromosome Deletion Chromosomes, Human, Pair 7 Fatal Outcome Females Femoral Fractures Femoral Neoplasms Homo sapiens Middle Aged Neoplasm Metastasis Nitrosourea Compounds Primary Myelofibrosis Sarcoma, Myeloid Thrombocythemia, Essential
5
(43.8%)
12481238
[Granulocytic sarcoma of the tonsils associated with myelodysplastic syndrome].
Geisse M, Mall G, Fritze D, Gartenschlager M.
Dtsch Med Wochenschr. 2002;127(50):2673-6.
Thrombocytopenia Anemia Fever Recurrent tonsillitis
BSG
Bone Marrow Homo sapiens Male Middle Aged Palatine Tonsil Peritonsillar Abscess Sarcoma, Myeloid Tonsillar Neoplasms Tonsillitis Tuberculosis, Miliary X-Ray Computed Tomography
6
(43.5%)
6945145
Ovarian granulocytic sarcoma as the primary manifestation of acute infantile myelomonocytic leukemia.
Morgan ER, Labotka RJ, Gonzalez-Crussi F, Wiederhold M, Sherman JO.
Cancer. 1981;48(8):1819-24.
Anemia Abdominal mass
Bone Marrow Cytoplasm Endoplasmic Reticulum Females Homo sapiens Infant Leukemia, Myelocytic, Acute Organ Size
7
(43.3%)
30352989
(6213823)
A Case of Granulocytic Sarcoma or Extramedullary Acute Myelomonocytic Leukemia of the Gallbladder.
Holzwanger EA, Alam Z, Hsu E, Hsu A, Mangano M, Kathman DL.
Am J Case Rep. 2018;19:1262-1266.
Jaundice Fever Leukocytosis
CD33 CD68
Differential Diagnosis Females Homo sapiens Sarcoma, Myeloid
7
(43.3%)
16778404
(2729966)
Isolated biliary granulocytic sarcoma followed by acute myelogeneous leukemia with multilineage dysplasia: a case report and literature review.
Sung CO, Ko YH, Park CK, Jang KT, Heo JS.
J Korean Med Sci. 2006;21(3):550-4.
Jaundice Leukemia Fever
Adult Bile Duct Neoplasms Cell Lineage Homo sapiens Leukemia, Myelocytic, Acute Male Sarcoma, Myeloid X-Ray Computed Tomography
9
(42.7%)
18717148
An unusual case of febrile neutropenia: acute myeloid leukemia presenting as myeloid sarcoma of the spleen.
Chen WL, Hsu YJ, Tsai WC, Tsao YT.
J Natl Med Assoc. 2008;100(8):957-9.
Neutropenia Fever Splenic abscess
Diagnostic Errors Differential Diagnosis Fatal Outcome Females Fever Homo sapiens Leukemia, Myelocytic, Acute Middle Aged Neutropenia Sarcoma, Myeloid Spleen Splenic Neoplasms X-Ray Computed Tomography
10
(39.1%)
1555189
Acute myelomonocytic leukemia with inv(16)(p13q22) complicating Philadelphia chromosome positive chronic myeloid leukemia.
Heim S, Christensen BE, Fioretos T, Sorensen AG, Pedersen NT.
Cancer Genet Cytogenet. 1992;59(1):35-8.
Splenomegaly Leukemia
Adult Blast Phase Bone Marrow Chromosomes, Human, Pair 16 Cytogenetics Homo sapiens Male
        

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