Gastrointestinal · Year 2 · from Gastrointestinal

Case 1: Acute Hepatitis B

Patient Presentation

Demographics: 28-year-old male

Chief Complaint: Fatigue, nausea, and dark urine for 10 days

History of Present Illness: The patient developed progressive fatigue, loss of appetite, and nausea over the past 2 weeks. He noticed his urine became dark "like cola" 10 days ago, followed by yellowing of his eyes. He reports right upper quadrant discomfort and low-grade fever. He has no prior history of liver disease.

Past Medical History: None

Social History: Reports unprotected sexual contact with new partner 3 months ago; denies IV drug use; no tattoos

Physical Examination

  • Vital Signs: Temperature 37.8C, HR 78 bpm, BP 118/72 mmHg
  • General: Ill-appearing jaundiced male
  • HEENT: Icteric sclerae, mild pharyngeal erythema
  • Abdomen: Tender hepatomegaly (liver edge 4 cm below costal margin), no splenomegaly, no ascites
  • Skin: Jaundice, no spider angiomata

Workup and Results

  • Liver Function Tests: AST 1,850 U/L, ALT 2,240 U/L (markedly elevated), Total bilirubin 8.4 mg/dL, Direct bilirubin 6.2 mg/dL, ALP 180 U/L
  • INR: 1.2 (mildly elevated)
  • Albumin: 3.6 g/dL
  • Hepatitis Serologies:
  • HBsAg: Positive
  • Anti-HBc IgM: Positive (indicates acute infection)
  • HBeAg: Positive (high replication)
  • Anti-HBs: Negative
  • HBV DNA: 8.2 x 10^7 IU/mL

Hepatitis B serologic markers over time during acute infection, showing the appearance and disappearance of HBsAg, anti-HBc IgM, HBeAg, and the eventual development of protective anti-HBs in patients who clear the infection.

Image Source: Wikimedia Commons, Public Domain

Diagnosis

Acute Hepatitis B Infection

Clinical Correlation

Hepatitis B virus is a partially double-stranded DNA virus transmitted through blood and body fluids. The incubation period is 6 weeks to 6 months. Acute infection is diagnosed by presence of HBsAg (surface antigen indicating active infection) and anti-HBc IgM (core antibody indicating acute infection). High HBeAg and HBV DNA levels indicate active viral replication. In immunocompetent adults, 95% clear the virus spontaneously. The marked transaminase elevation reflects immune-mediated hepatocyte destruction. Monitoring INR and mental status is critical to detect progression to acute liver failure, which occurs in <1% of acute HBV but has high mortality.

Treatment

  • Supportive care for most acute HBV (high spontaneous clearance rate)
  • Avoid hepatotoxic substances (alcohol, acetaminophen)
  • Monitor for signs of acute liver failure: worsening coagulopathy (INR >1.5), hepatic encephalopathy
  • Antiviral therapy (entecavir or tenofovir) indicated only if severe/fulminant course
  • Sexual contacts and household members should be tested and vaccinated
  • Follow-up serology at 6 months to confirm clearance (HBsAg negative, anti-HBs positive)
  • If HBsAg persists >6 months: chronic hepatitis B requiring treatment evaluation

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