Budd-Chiari syndrome risk factors: Difference between revisions
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==Risk Factors== | ==Risk Factors== | ||
* | *Approximately 80 percent of patients with the Budd-Chiari syndrome have an underlying disorder.Many patients may have more than one risk factor. Same patient may have multiple causes that predispose to the development of Budd-Chiari Syndrome. | ||
* | Associated risk factors include: | ||
* | *Hematologic disorders including: | ||
**Polycythemia rubra vera | |||
**Paroxysmal nocturnal hemoglobinuria | |||
**myeloproliferative disorder | |||
**Antiphospholipid antibody syndrome | |||
**Essential thrombocytosis | |||
**Inherited thrombotic diathesis | |||
*Coagulopathies include the following: | |||
**Protein C deficiency | |||
**Protein S deficiency | |||
**Antithrombin III deficiency | |||
**Factor V Leiden deficiency | |||
*Chronic infections like: | |||
**Hydatid cysts | |||
**Aspergillosis | |||
**Amebic abscess | |||
**Syphilis | |||
**Tuberculosis | |||
*Chronic inflammatory diseases such as: | |||
**Behçet disease | |||
**Inflammatory bowel disease | |||
**Sarcoidosis | |||
**Systemic lupus erythematosus | |||
**Sjögren syndrome | |||
**Mixed connective-tissue disease | |||
*Tumors such as | |||
**Hepatocellular carcinoma (HCC) | |||
**Renal cell carcinoma | |||
**Leiomyosarcoma | |||
**Adrenal carcinoma | |||
**Wilms tumor | |||
**Right atrial myxoma | |||
*Congenital membranous obstructions that includes the following: | |||
**Type I: Thin membrane is present in the vena cava or the atrium | |||
**Type II: A part of the vena cava is absent | |||
**Type III: The inferior vena cava (IVC) cannot be filled, and collaterals have developed | |||
*Miscellaneous risk factors of Budd-Chiari syndrome include the following: | |||
**Alpha1-antitrypsin deficiency | |||
**Dacarbazine | |||
**Urethane | |||
**Hypoplasia of the suprahepatic veins | |||
**Postsurgical obstruction | |||
**Posttraumatic obstruction | |||
**Total parenteral nutrition (TPN): Budd-Chiari syndrome can be a complication of TPN via an IVC catheter in a neonate | |||
==References== | ==References== |
Revision as of 10:22, 6 November 2017
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Risk Factors
- Approximately 80 percent of patients with the Budd-Chiari syndrome have an underlying disorder.Many patients may have more than one risk factor. Same patient may have multiple causes that predispose to the development of Budd-Chiari Syndrome.
Associated risk factors include:
- Hematologic disorders including:
- Polycythemia rubra vera
- Paroxysmal nocturnal hemoglobinuria
- myeloproliferative disorder
- Antiphospholipid antibody syndrome
- Essential thrombocytosis
- Inherited thrombotic diathesis
- Coagulopathies include the following:
- Protein C deficiency
- Protein S deficiency
- Antithrombin III deficiency
- Factor V Leiden deficiency
- Chronic infections like:
- Hydatid cysts
- Aspergillosis
- Amebic abscess
- Syphilis
- Tuberculosis
- Chronic inflammatory diseases such as:
- Behçet disease
- Inflammatory bowel disease
- Sarcoidosis
- Systemic lupus erythematosus
- Sjögren syndrome
- Mixed connective-tissue disease
- Tumors such as
- Hepatocellular carcinoma (HCC)
- Renal cell carcinoma
- Leiomyosarcoma
- Adrenal carcinoma
- Wilms tumor
- Right atrial myxoma
- Congenital membranous obstructions that includes the following:
- Type I: Thin membrane is present in the vena cava or the atrium
- Type II: A part of the vena cava is absent
- Type III: The inferior vena cava (IVC) cannot be filled, and collaterals have developed
- Miscellaneous risk factors of Budd-Chiari syndrome include the following:
- Alpha1-antitrypsin deficiency
- Dacarbazine
- Urethane
- Hypoplasia of the suprahepatic veins
- Postsurgical obstruction
- Posttraumatic obstruction
- Total parenteral nutrition (TPN): Budd-Chiari syndrome can be a complication of TPN via an IVC catheter in a neonate