Budd-Chiari syndrome causes: Difference between revisions
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==Overview== | ==Overview== | ||
Budd-Chiari syndrome is associated with a wide range of etiologies.On the basis of underlying cause Budd- Chairi can be Primary(75%) caused bythrombosis of the hepatic vein and Secondary (25%) caused by invasion/compression of the hepatic vein by an outside structure like(e.g. a tumor, abscess or cysts). | Budd-Chiari syndrome is associated with a wide range of etiologies.On the basis of underlying cause Budd- Chairi can be Primary(75%) caused bythrombosis of the hepatic vein and Secondary (25%) caused by invasion/compression of the hepatic vein by an outside structure like(e.g. a tumor, abscess or cysts).Causes include myeloproliferative disorders | ||
== Causes == | == Causes == | ||
Revision as of 16:47, 9 November 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief:
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Overview
Budd-Chiari syndrome is associated with a wide range of etiologies.On the basis of underlying cause Budd- Chairi can be Primary(75%) caused bythrombosis of the hepatic vein and Secondary (25%) caused by invasion/compression of the hepatic vein by an outside structure like(e.g. a tumor, abscess or cysts).Causes include myeloproliferative disorders
Causes
- Budd-Chiari syndrome is associated with a wide range of etiologies.[1][2][3][4]
- On the basis of underlying cause Budd- Chairi can be:
- Primary (75%): thrombosis of the hepatic vein
- Secondary (25%): invasion/compression of the hepatic vein by an outside structure like(e.g. a tumor, abscess or cysts)
Causes include:
- Myeloproliferative disorders:
- Myeloproliferative and other hemotologic abnormalities are one of the most common causes of Budd Chiari Syndrome.
- V617F mutation in Janus tyrosine kinase-2 (JAK2) is found in 80% of patients with polycythemia vera and 50% of patients with essential thrombocythemia or idiopathic myelofibrosis.Budd Chiari syndrome patients that test negative for this mutation should have bone marrow biopsy performed.
- Other associated hematologic causes include:
- Paroxysmal nocturnal hemoglobinuria
- Antiphospholipid syndrome
- factor V leiden mutation
- prothrombin gene mutation
- methylene tetrahydrofolate reductase gene mutation
- Malignancy
- Malignancy is commonly associated with compression or invasion of vessels and hypercoagulable state.
- Budd-Chiari is commonly associated with
- hepatocellular carcinoma(associated with membranous obstruction of inferior vena cava)
- adrenal gland or kidney malignancy
- right atrial sarcoma
- pancreatic cancer
- lung carcinoma
- gastric carcinoma
- Infections and benign liver lesions
- Cause extrinsic compression of inferior venacava. May be associated with hypercoagylable state. These lesions include:
- hepatic cysts and abscesses
- hepatic adenoma
- hepatic mucinous cystic neoplasm (cystadenoma)
- syphilitic gumma
- invasive aspergillosis
- zygomycosis (mucormycosis)
- aortic aneurysm
- Cause extrinsic compression of inferior venacava. May be associated with hypercoagylable state. These lesions include:
- Oral contraceptives and pregnancy
- Hypercoagulable state in women using oral contraceptives (for more than two weeks), pregnant , or those who have delivered a child within the previous two months accounts for nearly 20 percent of cases of the Budd-Chiari syndrome
- Other hypercoagulable states
Hypercoagulable conditions associated with Budd-Chiari include:
- G1691A factor V (Leiden) gene mutation associated with activated protein C resistance
- G20210A factor II gene mutation
- Antiphospholipid syndrome
- Antithrombin deficiency
- Protein C deficiency
- Protein S deficiency
- Paroxysmal nocturnal hemoglobinuria
- Behçet's syndrome
- Vasculitis in Behçet's syndrome can predispose to thrombosis.
- Membranous webs are usually are found near the entrance of the right hepatic vein into the inferior vena cava, may be due to a congenital anomaly or a myeloproliferative disease.
- More common in patients from South Africa, India, and Asia. Potentially treatable cause of Budd-chiari.
- Miscellaneous
- Miscellaneous causes of the Budd-Chiari syndrome include:
- Systemic lupus erythematosus
- Mixed-connective tissue disease
- Sjögren's syndrome
- inflammatory bowel disease
- hypereosinophilic syndrome
- idiopathic granulomatous venulitis
- sarcoidosis
- protein-losing enteropathy
- minimal change nephrotic syndrome
- neurofibromatosis
- alpha-1 antitrypsin deficiency
- trauma
- Miscellaneous causes of the Budd-Chiari syndrome include:
- Idiopathic
- Upto 20 percent of cases of the Budd-Chiari syndrome are idiopathic.
References
- ↑ Afredj N, Guessab N, Nani A, Faraoun SA, Ouled Cheikh I, Kerbouche R, Hannoun D, Amir ZC, Ait Kaci H, Bentabak K, Plessier A, Valla DC, Cazals-Hatem V, Denninger MH, Boucekkine T, Debzi N (2015). "Aetiological factors of Budd-Chiari syndrome in Algeria". World J Hepatol. 7 (6): 903–9. doi:10.4254/wjh.v7.i6.903. PMC 4411532. PMID 25937867.
- ↑ Lin M, Zhang F, Wang Y, Zhang B, Zhang W, Zou X, Zhang M, Zhuge Y (2017). "Liver cirrhosis caused by chronic Budd-Chiari syndrome". Medicine (Baltimore). 96 (34): e7425. doi:10.1097/MD.0000000000007425. PMC 5571988. PMID 28834866.
- ↑ Martens P, Nevens F (2015). "Budd-Chiari syndrome". United European Gastroenterol J. 3 (6): 489–500. doi:10.1177/2050640615582293. PMC 4669515. PMID 26668741.
- ↑ Merz WM, Rüland AM, Hippe V, Poetzsch B, Meyer C, Pollok JM, Gembruch U, Trebicka J (2016). "Pregnancy in Budd-Chiari Syndrome: Case Report and Proposed Risk Score". Medicine (Baltimore). 95 (22): e3817. doi:10.1097/MD.0000000000003817. PMC 4900734. PMID 27258526.