Budd-Chiari Syndrome: eMedicine Gastroenterology

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Budd-Chiari Syndrome: eMedicine Gastroenterology

emedicine.medscape.com

Overview: Budd-Chiari syndrome is an uncommon condition induced by thrombotic or nonthrombotic obstruction to hepatic venous outflow. Budd described it in 1845, and Chiari added the first pathologic description of a liver with obliterating endophlebitis of the ...

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Tags: Gastroenterology, Liver, Disease and Condition

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Most Recently Shared on June 2, 2010 at 7:29 pm By:

Health_SS Susan S

Budd-Chiari syndrome is an uncommon condition induced by obstruction to hepatic venous outflow. Learn more about it. http://bit.ly/cBBzpH

2 years ago...

Encephalopathy, Hepatic: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Definition Hepatic encephalopathy is a syndrome observed in patients with cirrhosis. Hepatic encephalopathy is defined as a spectrum of neuropsychiatric abnormalities in patients with liver dysfunction, after exclusion of other known brain disease. Hepatic encephalopathy is characterized by ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:58 pm By:

Health_SS Susan S Health Advocate

Hepatic encephalopathy is a syndrome observed in patients with cirrhosis. Learn more about hepatic encephalopathy. http://bit.ly/csoGNV

2 years ago...

Peutz-Jeghers Syndrome: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Peutz-Jeghers syndrome (PJS) is an autosomal dominant inherited disorder characterized by intestinal hamartomatous polyps in association with mucocutaneous melanocytic macules. Although the intestinal lesions are hamartomas, patients with Peutz-Jeghers syndrome (PJS) have a 15-fold increased risk ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:56 pm By:

Health_SS Susan S Health Advocate

The cause of Peutz-Jeghers syndrome (PJS) appears to be a germline mutation of the STK11/LKB1 tumor suppressor gene. http://bit.ly/95pLNc

2 years ago...

Hepatorenal Syndrome: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Hepatorenal syndrome (HRS) is the development of renal failure in patients with advanced chronic liver disease,1 occasionally fulminant hepatitis, who have portal hypertension and ascites. Estimates indicate that at least 40% of patients with cirrhosis ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:47 pm By:

SusanS_Health Susan Scroggins Active Health Library and Health Advocate

Hepatorenal syndrome (HRS) is the development of renal failure in patients with advanced chronic liver disease. http://bit.ly/blmq2o

2 years ago...

Intestinal Pseudo-obstruction, Surgical Treatment: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: The term intestinal pseudo-obstruction is used to indicate a syndrome characterized by a clinical picture suggestive of mechanical obstruction in the absence of any demonstrable evidence of such an obstruction in the intestine.1 Based on clinical ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:42 pm By:

J_Bohlen Julie Bohlen Health Executive and Active Health Library

Learn more information about the surgical treatment of an intestinal pseudo-obstruction. http://bit.ly/9fvVMe

2 years ago...

Crigler-Najjar Syndrome: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Crigler-Najjar syndrome (CNS) is a rare autosomal recessive disorder of bilirubin metabolism. Two distinct forms have been described, as follows: type 1 and type 2. Type 1 Crigler-Najjar syndrome, first described in 1952 by Crigler and ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:42 pm By:

J_Bohlen Julie Bohlen Health Executive and Active Health Library

Crigler-Najjar syndrome is a rare autosomal recessive disorder of bilirubin metabolism. Learn about the 2 types. http://bit.ly/9J8oSi

2 years ago...

Portal-Systemic Encephalopathy: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Portosystemic encephalopathy (PSE) or hepatic encephalopathy (HE) is a neuropsychiatric syndrome associated with hepatocellular failure or portal-systemic venous shunting. There has been a lack of standardization of terminology used to define hepatic encephalopathy. Acute hepatic encephalopathy ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:41 pm By:

SusanS_Health Susan Scroggins Active Health Library and Health Advocate

Portosystemic encephalopathy is a neuropsychiatric syndrome associated w/ ehpatocellular failure. Learn more. http://bit.ly/cdCgU3

2 years ago...

Whipple Disease: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Whipple disease is a systemic disease most likely caused by a gram-positive bacterium, Tropheryma whippelii.1, 2 Although the first descriptions of the disorder described a malabsorption syndrome with small intestine involvement, the disease also affects ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:29 pm By:

Health_SS Susan S Health Advocate

Whipple disease is a systemic disease most likely caused by a gram-positive bacterium, Tropheryma whippelii. http://bit.ly/c4TTz3

2 years ago...

Gilbert Syndrome: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Augustine Gilbert and Pierre Lereboullet first described Gilbert syndrome, the most common inherited cause of unconjugated hyperbilirubinemia, in 1901. This autosomal recessive condition is characterized by intermittent jaundice in the absence of hemolysis or underlying liver ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:29 pm By:

Health_SS Susan S Health Advocate

Gilbert syndrome is characterized by intermittent jaundice in the absence of hemolysis or underlying liver disease. http://bit.ly/bfPylX

2 years ago...

Familial Adenomatous Polyposis: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Familial adenomatous polyposis (FAP) is the most common adenomatous polyposis syndrome. It is an autosomal dominant inherited disorder characterized by the early onset of hundreds to thousands of adenomatous polyps throughout the colon. If left untreated, ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:28 pm By:

SusanS_Health Susan Scroggins Active Health Library and Health Advocate

Familial adenomatous polyposis (FAP) is the most common adenomatous polyposis syndrome. Learn more about FAP. http://bit.ly/btE28k

2 years ago...

Sprue, Tropical: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Tropical sprue (TS) is a syndrome characterized by acute or chronic diarrhea, weight loss, and malabsorption of nutrients. It occurs in residents of or visitors to the tropics and subtropics. The first description of tropical sprue ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:26 pm By:

SusanS_Health Susan Scroggins Active Health Library and Health Advocate

Tropical sprue (TS) is a syndrome characterized by acute or chronic diarrhea, weight loss & malabsorption of nutrients. http://bit.ly/bZ1hIm

2 years ago...

Dubin-Johnson Syndrome: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Dubin-Johnson syndrome (DJS) is a type of hereditary hyperbilirubinemia that was first described independently in 1954 by Dubin and Johnson and by Sprinz and Nelson. Hereditary hyperbilirubinemias can be divided into conjugated forms and unconjugated forms. ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:24 pm By:

Health_SS Susan S Health Advocate

Dubin-Johnson syndrome (DJS) is a type of hereditary hyperbilirubinemia. It can be divided into 2 classes. Learn more. http://bit.ly/9VOokx

2 years ago...

Zollinger-Ellison Syndrome: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Zollinger-Ellison syndrome (ZES) is caused by a non-beta islet cell, gastrin-secreting tumor of the pancreas that stimulates the acid-secreting cells of the stomach to maximal activity, with consequent gastrointestinal mucosal ulceration. ZES may occur sporadically or ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:24 pm By:

SusanS_Health Susan Scroggins Active Health Library and Health Advocate

Zollinger-Ellison syndrome may occur sporadically or as part of an autosomal dominant familial syndrome. Learn more. http://bit.ly/aK8g1w

2 years ago...

WDHA Syndrome: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: In 1957, Priest and Alexander reported a patient with peptic ulcer, diarrhea, hypokalemia, and an islet cell tumor.1 However, the first complete description of the syndrome of watery diarrhea, hypokalemia, and achlorhydria (ie, WDHA syndrome) ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:21 pm By:

Health_SS Susan S Health Advocate

WDHA syndrome is a condition associated with watery diarrhea, hypokalemia, and achlorhydria. Learn more about WDHA. http://bit.ly/9Eqe2G

2 years ago...

Alcoholic Hepatitis: eMedicine Gastroenterology

emedicine.medscape.com — “Overview: Alcoholic hepatitis is a syndrome of progressive inflammatory liver injury associated with long-term heavy intake of ethanol. The pathogenesis is not completely understood.1Patients who are severely affected present with subacute onset of fever, hepatomegaly, leukocytosis, ...View full resource at emedicine.medscape.com

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Most Recently Shared on June 2, 2010 at 7:16 pm By:

SusanS_Health Susan Scroggins Active Health Library and Health Advocate

Alcoholic hepatitis is a syndrome of progressive inflammatory liver injury associated with long-term heavy drinking. http://bit.ly/9LUFHt

2 years ago...

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