Banti's syndrome
(Redirected from Banti's disease)
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Banti's syndrome | |
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Synonyms | Banti's disease |
Pronounce | N/A |
Specialty | N/A |
Symptoms | Splenomegaly, anemia, leukopenia, thrombocytopenia, portal hypertension |
Complications | Esophageal varices, ascites, hepatic encephalopathy |
Onset | Typically in adulthood |
Duration | Chronic |
Types | N/A |
Causes | Unknown, possibly related to portal hypertension |
Risks | Chronic liver disease, cirrhosis |
Diagnosis | Clinical examination, imaging studies, blood tests |
Differential diagnosis | Cirrhosis, myeloproliferative disorders, lymphoma |
Prevention | N/A |
Treatment | Splenectomy, beta blockers, endoscopic therapy |
Medication | N/A |
Prognosis | Variable, depends on complications |
Frequency | Rare |
Deaths | N/A |
Banti's Syndrome is a rare and chronic disease characterized by the enlargement of the spleen (splenomegaly) and hypertension in the portal vein system, which carries blood from the gastrointestinal tract and spleen to the liver. The syndrome was first described by the Italian physician Guido Banti in 1898, hence the name.
Etiology
The exact cause of Banti's Syndrome is unknown. However, it is believed to be associated with various conditions that cause increased pressure in the portal vein system, such as liver cirrhosis, hepatitis, and thrombosis of the portal vein.
Symptoms
The primary symptoms of Banti's Syndrome include an enlarged spleen, anemia, and gastrointestinal bleeding. Other symptoms may include fatigue, abdominal pain, and jaundice.
Diagnosis
Diagnosis of Banti's Syndrome is typically based on the clinical symptoms, physical examination, and imaging studies such as ultrasound, computed tomography (CT) scan, and magnetic resonance imaging (MRI). Blood tests may also be performed to assess liver function and the presence of anemia.
Treatment
Treatment of Banti's Syndrome primarily involves managing the underlying condition causing portal hypertension. This may include medication to reduce blood pressure, endoscopic procedures to stop gastrointestinal bleeding, and in severe cases, liver transplantation. Splenectomy, the surgical removal of the spleen, may also be performed to alleviate symptoms.
Prognosis
The prognosis of Banti's Syndrome largely depends on the severity of the underlying condition and the patient's response to treatment. With appropriate management, the symptoms of Banti's Syndrome can often be controlled, and the patient's quality of life can be significantly improved.
See also
NIH genetic and rare disease info
Banti's syndrome is a rare disease.
Rare and genetic diseases | ||||||
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Rare diseases - Banti's syndrome
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Hepatology | ||||||||||
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Health science - Medicine - Gastroenterology - edit |
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Diseases of the esophagus - stomach |
Halitosis | Nausea | Vomiting | GERD | Achalasia | Esophageal cancer | Esophageal varices | Peptic ulcer | Abdominal pain | Stomach cancer | Functional dyspepsia | Gastroparesis |
Diseases of the liver - pancreas - gallbladder - biliary tree |
Hepatitis | Cirrhosis | NASH | PBC | PSC | Budd-Chiari | Hepatocellular carcinoma | Acute pancreatitis | Chronic pancreatitis | Pancreatic cancer | Gallstones | Cholecystitis |
Diseases of the small intestine |
Peptic ulcer | Intussusception | Malabsorption (e.g. Coeliac, lactose intolerance, fructose malabsorption, Whipple's) | Lymphoma |
Diseases of the colon |
Diarrhea | Appendicitis | Diverticulitis | Diverticulosis | IBD (Crohn's, Ulcerative colitis) | IBS | Constipation | Colorectal cancer | Hirschsprung's | Pseudomembranous colitis |
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Contributors: Prab R. Tumpati, MD