Budd-Chiari syndrome causes: Difference between revisions
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{{Budd-Chiari syndrome}} | {{Budd-Chiari syndrome}} | ||
{{CMG}}; {{AE}} | {{CMG}}; {{AE}}{{Mazia}} | ||
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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 | Budd-Chiari syndrome is associated with a wide range of [[etiologies]]. On the basis of underlying cause Budd- Chairi syndrome can be primary (75%) caused by [[thrombosis]] of the [[Hepatic veins|hepatic vein]] or secondary (25%) caused by [[invasion]]/compression of the [[Hepatic veins|hepatic vein]] by an outside structure such as a [[tumor]], [[abscess]] or [[cysts]]. Causes include [[Myeloproliferative disease|myeloproliferative disorders]], [[malignancy]], [[paroxysmal nocturnal hemoglobinuria]], [[antiphospholipid syndrome]], [[Factor V Leiden mutation|factor V leiden mutation]], [[infections]] and [[Liver lesions|benign liver lesions]], [[oral contraceptives]] and [[pregnancy]], [[hypercoagulable states]], [[Behçet's syndrome]], membranous webs. | ||
== Causes == | == Causes == | ||
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**[[Vasculitis]] in [[Behçet's syndrome]] can predispose to [[thrombosis]]. | **[[Vasculitis]] in [[Behçet's syndrome]] can predispose to [[thrombosis]]. | ||
*Membranous webs are usually are found near the entrance of the [[Hepatic vein|right hepatic vein]] into the [[Inferior vena cavae|inferior vena cava]], may be due to a [[congenital anomaly]] or a [[myeloproliferative disease]]. | *Membranous webs are usually are found near the entrance of the [[Hepatic vein|right hepatic vein]] into the [[Inferior vena cavae|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: | ||
**Miscellaneous causes of the Budd-Chiari syndrome include: | **Miscellaneous causes of the Budd-Chiari syndrome include: | ||
***[[Systemic lupus erythematosus]] | ***[[Systemic lupus erythematosus]] | ||
***Mixed-connective tissue disease | ***[[Mixed connective tissue disease|Mixed-connective tissue disease]] | ||
***[[Sjögren's syndrome]] | ***[[Sjögren's syndrome]] | ||
***[[ | ***[[Inflammatory bowel disease]] | ||
***[[ | ***[[Hypereosinophilic syndrome]] | ||
*** | ***Idiopathic granulomatous venulitis | ||
***[[ | ***[[Sarcoidosis]] | ||
***[[ | ***[[Protein losing enteropathy|Protein-losing enteropathy]] | ||
*** | ***[[Minimal change disease]] | ||
***[[ | ***[[Neurofibromatosis]] | ||
***[[ | ***[[Alpha 1-antitrypsin deficiency|Alpha-1 antitrypsin deficiency]] | ||
***[[ | ***[[Trauma]] | ||
*[[Idiopathic]] | *[[Idiopathic]]: | ||
**Upto 20 percent of cases of the Budd-Chiari syndrome are [[idiopathic]]. | **Upto 20 percent of cases of the Budd-Chiari syndrome are [[idiopathic]]. | ||
Latest revision as of 17:00, 30 November 2017
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Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1]; Associate Editor(s)-in-Chief: Mazia Fatima, MBBS [2]
Overview
Budd-Chiari syndrome is associated with a wide range of etiologies. On the basis of underlying cause Budd- Chairi syndrome can be primary (75%) caused by thrombosis of the hepatic vein or secondary (25%) caused by invasion/compression of the hepatic vein by an outside structure such as a tumor, abscess or cysts. Causes include myeloproliferative disorders, malignancy, paroxysmal nocturnal hemoglobinuria, antiphospholipid syndrome, factor V leiden mutation, infections and benign liver lesions, oral contraceptives and pregnancy, hypercoagulable states, Behçet's syndrome, membranous webs.
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 renal malignancy
- right atrial sarcoma
- pancreatic cancer
- lung carcinoma
- gastric carcinoma
- Infections and benign liver lesions
- Cause extrinsic compression of inferior vena cava. May be associated with hypercoagulable 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:
- 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:
- 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.