Cirrhosis differential diagnosis: Difference between revisions

Jump to navigation Jump to search
No edit summary
Line 1: Line 1:
__NOTOC__
__NOTOC__
{{Cirrhosis}}
{{Cirrhosis}}
{{CMG}} {{AE}} {{CP}}}
{{CMG}} {{AE}} {{CP}}}{{Cherry}}


==Overview==
==Overview==

Revision as of 11:53, 19 December 2017

Cirrhosis Microchapters

Home

Patient Information

Overview

Historical Perspective

Classification

Pathophysiology

Causes

Differentiating Cirrhosis from other Diseases

Epidemiology and Demographics

Risk Factors

Screening

Natural History, Complications and Prognosis

Diagnosis

Diagnostic Study of Choice

History and Symptoms

Physical Examination

Laboratory Findings

Electrocardiogram

Chest X Ray

CT

MRI

Echocardiography or Ultrasound

Other Imaging Findings

Other Diagnostic Studies

Treatment

Medical Therapy

Surgery

Primary Prevention

Secondary Prevention

Tertiary Prevention

Cost-Effectiveness of Therapy

Future or Investigational Therapies

Case studies

Case #1

Cirrhosis differential diagnosis On the Web

Most recent articles

cited articles

Review articles

CME Programs

Powerpoint slides

Images

American Roentgen Ray Society Images of Cirrhosis differential diagnosis

All Images
X-rays
Echo & Ultrasound
CT Images
MRI

Ongoing Trials at Clinical Trials.gov

US National Guidelines Clearinghouse

NICE Guidance

FDA on Cirrhosis differential diagnosis

CDC on Cirrhosis differential diagnosis

Cirrhosis differential diagnosis in the news

Blogs on Cirrhosis differential diagnosis

Directions to Hospitals Treating Cirrhosis

Risk calculators and risk factors for Cirrhosis differential diagnosis

Editor-In-Chief: C. Michael Gibson, M.S., M.D. [1] Associate Editor(s)-in-Chief: Charmaine Patel, M.D. [2]}Sudarshana Datta, MD [3]

Overview

Cirrhosis can present in a similar way to some other diseases. History, physical examination, and diagnostic testing can help to differentiate cirrhosis from other diseases such as malignancy, constrictive pericarditis, Budd-Chiari syndrome, portal vein thrombosis and splenic vein thrombosis.

Differentiating Cirrhosis from other Diseases

Differential diagnosis of cirrhosis on the basis of jaundice is as follows: [1]

Classification of jaundice based on etiology Disease History and clinical manifestations Diagnosis
Lab Findings Other blood tests Other diagnostic
Family history Fever RUQ Pain Pruritis AST ALT ALK BLR Indirect BLR Direct Viral serology
Jaundice Hepatocellular Jaundice Hemochromatosis + - -/+ - ↑/N ↑/N N - Ferritin ↑ Liver biopsy
Wilson's disease + - -/+ - N ↑/N N - Serum cerulloplasmin ↑ Liver biopsy
Viral hepatitis - -/+ - - N ↑/N N + Specific viral antibody for each type -
Alcoholic hepatitis - -/+ -/+ - ↑↑ N ↑/N N - - -
Drug induced hepatitis - -/+ - - N ↑/N N - - -
Autoimmune hepatitis -/+ - - -/+ N ↑/N N - Anti-LKM antibody Liver biopsy
Cirrhosis -/+ -/+ -/+ - ↑/N ↑/N ↑/N -/+ Low platate Small liver on ultrasond
Cholestatic Jaundice Common bile duct stone -/+ - + + N N N - Dilated ducts on sono CT/ERCP
Hepatitis A cholestatic type - -/+ + + N N N + HAV- AB Abdominal ultrasound
EBV / CMV hepatitis - -/+ + + N N N + Positive serology
Primary biliary cirrhosis -/+ - -/+ + N/↑ N/↑ N - AMA positive Liver biopsy
Primary sclerosing cholangitis -/+ - -/+ + N/↑ N/↑ N - Beading on MRCP Liver biopsy
Pancreatic carcinoma + - -/+ - N/↑ N/↑ N - Mass on ultrasond CT scan for diagnosis
Isolated Jaundice Crigler-Najjar type 2 + - - - N N N - Genetic testing
Gilbert + - - - N N N - Genetic testing
Rotor syndrome + - - - N N N N - Genetic testing Liver biopsy
Dubin-Johnson syndrome + - - - N N N N - Genetic testing Liver biopsy
Hereditory spherocytosis + - -/+ - N N N N - Genetic testing Osmotic fragility
G6PD deficiency + - - - N N N N - Genetic testing
Thalassemia + - - - N N N N - Genetic testing
Sickle cell disease + - - - N N N N - Genetic testing
Paroxismal nocturnal hemoglobinoria - - - - N N N N - Flocytometery
Immune hemolysis - -/+ - - N N N N - Autoantibodies
Hematoma - -/+ - - N N N N - Anemia Truma or surgery in history
Condition Differentiating Signs and Symptoms Differentiating Tests
Constrictive pericarditis Increased jugular venous pressure, atrial fibrillation, and tachycardia. Quiet heart sounds with a third heart sound (ventricular knock) present. EKG will show tachycardia, atrial fibrillation, low-voltage QRS complexes and T wave abnormalities. Doppler ultrasound will show ventricular filling abnormalities.
Budd-Chiari Syndrome Abdominal pain, diarrhea, and worsening ascites. Doppler ultrasound and CT of the abdomen will show absence of the hepatic vein filling. Abdominal CT will show a rapid clearing of the caudate lobe of the liver.
Splenic vein thrombosis Similar signs and symptoms of acute pancreatitis with upper abdominal pain radiating to the back, vomiting, poor bowel sounds, fever and shock. Cullen's sign and Grey-Turner's sign may be present. An ultrasound of the abdomen and CT will show evidence of a splenic vein thrombosis. Normal hepatic venous pressure gradient is present.
Portal vein thrombosis Will depend on the underlying cause. If pancreatitis is present, upper abdominal pain radiating to the back, vomiting, poor bowel sounds, fever and shock. Cullen's sign and Grey-Turner's sign may be present. If the cause is ascending cholangitis, fever, rigors, right upper quadrant pain, dark urine, and pale stools may be seen. If abdominal sepsis is the cause, fever, abdominal pain and other signs of peritonitis will be seen. Doppler ultrasound and abdominal CT will show a portal vein filling defect, and absence of flow in the portal vein. MR or direct angiography will show a normal hepatic venous pressure gradient.
Schistosomiasis History of travel to endemic areas. Constitutional symptoms such as malaise, rigors, anorexia, weight loss, vomiting, diarrhea, headache, muscular aches, weakness and abdominal pain. Also urticaria, fever and lymphadenopathy may be seen. MR or direct angiography will show a normal hepatic venous pressure gradient.
Sarcoidosis Dry cough with dyspnea. Anterior or posterior uveitis, dry eyes and glaucoma. Skin findings may include maculopapular lesions on the face, back, arms and legs, and erythema nodosum on the legs. Chest x ray may show hilar lymphadenopathy, upper lobe fibrosis, and diffuse reticulonodular shadowing. Liver biopsy will show non-necrotizing, non-caseating granulomas.
Inferior vena cava obstruction Signs and symptoms of renal cell carcinoma, with hematuria, flank pain, flank or abdominal mass, weight loss and hypertension. Ultrasound of the abdomen will show evidence of inferior vena cava obstruction.
Nodular regenerative hyperplasia None Liver biopsy will show small regenerative nodules with little or no fibrosis on reticulin staining.
Idiopathic portal hypertension (hepatoportal sclerosis) None Liver biopsy will show no evidence of cirrhosis.
Vitamin A intoxication, arsenic, and vinyl chloride toxicity None History generally reveals exposure.


Differentiating Cirrhosis from other Diseases Based on Ascitic Fluid

Ascites may be caused by portal hypertension due to cirrhosis of liver or due to other causes such as malignancy.Ascitic fluid analysis should be done to broadly categorize the cause of ascites.

Ascites is broadly classified as two types based on the serum-ascites albumin gradient (SAAG):

  • Transudate - SAAG > 1.1 g/dL (indicates the ascites is due to portal hypertension).
  • Exudate - SAAG < 1.1 g/dL (indicates the ascites is due to non-portal hypertension etiology).

References

  1. Fargo MV, Grogan SP, Saguil A (2017). "Evaluation of Jaundice in Adults". Am Fam Physician. 95 (3): 164–168. PMID 28145671.

Template:WS Template:WH