Budd-Chiari syndrome

Budd-Chiari syndrome (BCS) is caused by obstruction of hepatic venous outflow involving either the hepatic veins or the terminal segment of the inferior vena cava.



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Narrow down the case reports



Total: 600 (papers)

  


(per page)
Matched Phenotype  Gene  Mutation  MeSH
Rank
(Similarity)
PMID
(PMCID)
566
(5.0%)
3683091
Leiomyosarcoma of the inferior vena cava presenting as Budd-Chiari syndrome.
Taylor RW, Sylwestrowicz T, Kossakowska AE, Urbanski SJ, Minuk GY.
Liver. 1987;7(4):201-5.
Neoplasm
Budd-Chiari Syndrome Homo sapiens Immunohistochemistry Male
566
(5.0%)
2491049
[Serious vascular complications in malignant carcinoid tumor].
Estrada Saiz RV, Sanchez de las Matas Sanchez I, Garcia Paredes J.
An Med Interna. 1989;6(10):534-6.
Carcinoid tumor
Adult Budd-Chiari Syndrome Circulating Neoplastic Cells Females Homo sapiens Male Malignant Carcinoid Syndrome Middle Aged Neoplasm Invasiveness Neoplasm Metastasis Thrombosis
566
(5.0%)
2208888
The hot stripe sign. An unusual variation.
Palestro CJ, Fineman DS, Goldsmith SJ.
Clin Nucl Med. 1990;15(9):647.
Breast carcinoma
Breast Females Homo sapiens Liver Middle Aged Radionuclide Imaging Spleen
566
(5.0%)
2078257
Budd Chiari syndrome in a post partum female with adrenal cortical carcinoma. Case report and review of the literature.
Gonzalez Keelan C, Gurrea C, Ramirez I.
Bol Asoc Med P R. 1990;82(12):538-40.
Carcinoma
Adult Budd-Chiari Syndrome Carcinoma Females Homo sapiens Postpartum Period
566
(5.0%)
1821635
[Retroperitoneal myxoid liposarcoma of the kidney capsule as a cause of Budd-Chiari syndrome].
Grutzner G, Furst G, Kuhn FP, Kliche KO.
Aktuelle Radiol. 1991;1(6):308-11.
Lipoma
Budd-Chiari Syndrome Females Homo sapiens Kidney Neoplasm Magnetic Resonance Imaging Retroperitoneal Neoplasms X-Ray Computed Tomography
566
(5.0%)
1547037
[Orthotopic liver transplantation in the Budd-Chiari syndrome. A case report].
Sanchez Bueno F, Parrilla P, Ramirez P, Miras M, Robles R, Pons JA, Acosta F, Nunez R, Bermejo J, Rodriguez JM, et al..
Rev Esp Enferm Dig. 1992;81(1):52-6.
Encephalopathy
Adult Budd-Chiari Syndrome Females Hepatectomy Homo sapiens Liver
566
(5.0%)
1523708
Budd-Chiari syndrome complicating lung carcinoma of the right inferior lobe: a case report.
Muretto P.
Tumori. 1992;78(2):147-9.
Carcinoma
Bronchogenic Carcinoma Budd-Chiari Syndrome Females Homo sapiens Lung Neoplasms Neoplasm Invasiveness
566
(5.0%)
1221115
[Reversal of portal flow by obstruction of the hepatic veins by hepatic tumours (author's transl)].
L'hermine C, Paris JC, Dehaene JL, Villoutreix H, Denies JL.
J Radiol Electrol Med Nucl. 1975;56(4):299-306.
Carcinoma
Adult Celiac Artery Females Homo sapiens Male Middle Aged Regional Blood Flow
566
(5.0%)
1008048
Possible response of acute psychosis in hepatic encephalopathy to levodopa.
Douer D, Weinberger A, Naftalin J, Pinkhas J, De Vries A.
Am J Gastroenterol. 1976;66(5):473-5.
Psychosis
Adult Budd-Chiari Syndrome Hepatic Encephalopathy Homo sapiens Male Neurocognitive Disorders
566
(5.0%)
948598
Pseudo-metastases in the liver: a presentation of the Budd-Chiari syndrome.
Hungerford GD, Hamlyn AN, Lunzer MR, Dick R, Sherlock S.
Radiology. 1976;120(3):627-8.
Neoplasm
Adult Biopsy Budd-Chiari Syndrome Contraceptives, Oral, Hormonal Differential Diagnosis Females Homo sapiens Neoplasm Metastasis Radionuclide Imaging Technetium
        

Phenotype(s) retrieved from Orphanet

    Total: 18

HPO ID Term Frequency
HP:0001409 Portal hypertension Very frequent (99-80%)
HP:0001541 Ascites Very frequent (99-80%)
HP:0001744 Splenomegaly Very frequent (99-80%)
HP:0001394 Cirrhosis Frequent (79-30%)
HP:0001945 Fever Frequent (79-30%)
HP:0002027 Abdominal pain Frequent (79-30%)
HP:0002040 Esophageal varix Frequent (79-30%)
HP:0002240 Hepatomegaly Frequent (79-30%)
HP:0002910 Elevated hepatic transaminase Frequent (79-30%)
HP:0000952 Jaundice Occasional (29-5%)
HP:0001082 Cholecystitis Occasional (29-5%)
HP:0001824 Weight loss Occasional (29-5%)
HP:0002024 Malabsorption Occasional (29-5%)
HP:0002239 Gastrointestinal hemorrhage Occasional (29-5%)
HP:0002586 Peritonitis Occasional (29-5%)
HP:0005214 Intestinal obstruction Occasional (29-5%)
HP:0005244 Gastrointestinal infarctions Occasional (29-5%)
HP:0006554 Acute hepatic failure Occasional (29-5%)


Phenotype(s) retrieved from case reports

    Total: 126

HPO ID Term # of case reports
HP:0001541 Ascites 51
HP:0001394 Cirrhosis 40
HP:0030243 Hepatic vein thrombosis 29
HP:0001409 Portal hypertension 27
HP:0002027 Abdominal pain 23
HP:0030242 Portal vein thrombosis 15
HP:0002240 Hepatomegaly 14
HP:0004936 Venous thrombosis 14
HP:0000969 Edema 12
HP:0100279 Ulcerative colitis 12
HP:0002204 Pulmonary embolism 10
HP:0100724 Hypercoagulability 10
HP:0025343 Lupus anticoagulant 9
HP:0000952 Jaundice 6
HP:0001399 Hepatic failure 6
HP:0002617 Dilatation 6
HP:0012115 Hepatitis 6
HP:0002480 Hepatic encephalopathy 5
HP:0030731 Carcinoma 5
HP:0000822 Hypertension 4
HP:0001903 Anemia 4
HP:0001907 Thromboembolism 4
HP:0002563 Constrictive pericarditis 4
HP:0006562 Viral hepatitis 4
HP:0012175 Resistance to activated protein C 4
HP:0001297 Stroke 3
HP:0001396 Cholestasis 3
HP:0001658 Myocardial infarction 3
HP:0001733 Pancreatitis 3
HP:0001873 Thrombocytopenia 3
HP:0001945 Fever 3
HP:0001971 Hypersplenism 3
HP:0002040 Esophageal varix 3
HP:0002625 Deep venous thrombosis 3
HP:0002664 Neoplasm 3
HP:0100523 Liver abscess 3
HP:0100806 Sepsis 3
HP:0000100 Nephrotic syndrome 2
HP:0001824 Weight loss 2
HP:0002013 Vomiting 2
HP:0002045 Hypothermia 2
HP:0002090 Pneumonia 2
HP:0002202 Pleural effusion 2
HP:0002243 Protein-losing enteropathy 2
HP:0002488 Acute leukemia 2
HP:0002605 Hepatic necrosis 2
HP:0002613 Biliary cirrhosis 2
HP:0002619 Varicose veins 2
HP:0002861 Melanoma 2
HP:0003641 Hemoglobinuria 2
HP:0004418 Thrombophlebitis 2
HP:0005305 Cerebral venous thrombosis 2
HP:0011473 Villous atrophy 2
HP:0025615 Abscess 2
HP:0030151 Cholangitis 2
HP:0030169 Gastric varix 2
HP:0031273 Shock 2
HP:0200042 Skin ulcer 2
HP:0200123 Chronic hepatitis 2
HP:0410019 Epigastric pain 2
HP:0000093 Proteinuria 1
HP:0000238 Hydrocephalus 1
HP:0000709 Psychosis 1
HP:0000819 Diabetes mellitus 1
HP:0000988 Skin rash 1
HP:0001048 Cavernous hemangioma 1
HP:0001082 Cholecystitis 1
HP:0001336 Myoclonus 1
HP:0001395 Hepatic fibrosis 1
HP:0001413 Micronodular cirrhosis 1
HP:0001635 Congestive heart failure 1
HP:0001655 Patent foramen ovale 1
HP:0001735 Acute pancreatitis 1
HP:0001876 Pancytopenia 1
HP:0001880 Eosinophilia 1
HP:0001894 Thrombocytosis 1
HP:0001909 Leukemia 1
HP:0001953 Diabetic ketoacidosis 1
HP:0002014 Diarrhea 1
HP:0002018 Nausea 1
HP:0002024 Malabsorption 1
HP:0002196 Myelopathy 1
HP:0002239 Gastrointestinal hemorrhage 1
HP:0002248 Hematemesis 1
HP:0002527 Falls 1
HP:0002571 Achalasia 1
HP:0002588 Duodenal ulcer 1
HP:0002615 Hypotension 1
HP:0002829 Arthralgia 1
HP:0003073 Hypoalbuminemia 1
HP:0003075 Hypoproteinemia 1
HP:0003228 Hypernatremia 1
HP:0003270 Abdominal distention 1
HP:0003419 Low back pain 1
HP:0004420 Arterial thrombosis 1
HP:0005112 Abdominal aortic aneurysm 1
HP:0005521 Disseminated intravascular coagulation 1
HP:0005558 Chronic leukemia 1
HP:0006580 Portal fibrosis 1
HP:0006772 Renal angiomyolipoma 1
HP:0011675 Arrhythmia 1
HP:0011854 Hemoperitoneum 1
HP:0011974 Myelofibrosis 1
HP:0012050 Anasarca 1
HP:0012418 Hypoxemia 1
HP:0012578 Membranous nephropathy 1
HP:0025142 Constitutional symptom 1
HP:0025322 Venous occlusion 1
HP:0025324 Arterial occlusion 1
HP:0030017 Vaginismus 1
HP:0030065 Primitive neuroectodermal tumor 1
HP:0030148 Heart murmur 1
HP:0030955 Alcoholism 1
HP:0031368 Intestinal perforation 1
HP:0031369 Colon perforation 1
HP:0032061 Hypereosinophilia 1
HP:0032154 Aphthous ulcer 1
HP:0040319 Dark urine 1
HP:0100570 Carcinoid tumor 1
HP:0100584 Endocarditis 1
HP:0100598 Pulmonary edema 1
HP:0100601 Eclampsia 1
HP:0100790 Hernia 1
HP:0100817 Renovascular hypertension 1
HP:0200036 Skin nodule 1
HP:0200120 Chronic active hepatitis 1


Causative gene(s) retrieved from Orphanet

    Total: 2

Gene Symbol Gene Name Entrez Gene ID
F5 coagulation factor V 2153
JAK2 Janus kinase 2 3717