Definition
Glandular fever, also known as infectious mononucleosis, is an acute viral illness most commonly caused by Epstein–Barr virus (EBV), a member of the herpesvirus family. It is characterized by fever, sore throat, lymphadenopathy, and fatigue. The condition is self-limiting but may be associated with prolonged convalescence and, in rare cases, serious complications.
Etiology and Transmission
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Primary cause: Epstein–Barr virus (EBV)
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Less common causes: Cytomegalovirus (CMV), human herpesvirus 6 (HHV-6), HIV (acute infection), toxoplasmosis (mimics presentation)
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Transmission:
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Primarily via saliva (“kissing disease”)
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Less commonly via sexual contact, blood transfusion, or organ transplantation
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Incubation period: Typically 4–6 weeks after exposure
Pathophysiology
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EBV infects oropharyngeal epithelial cells and subsequently B lymphocytes via CD21 receptors.
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Infected B cells proliferate, triggering a robust cytotoxic T-cell response responsible for many symptoms.
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This immune activation causes lymphoid tissue enlargement (lymph nodes, spleen, tonsils) and systemic symptoms.
Risk Factors
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Adolescents and young adults (15–25 years old) are most commonly affected.
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Close personal contact with infected individuals.
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Immunocompromised states increase severity and duration.
Clinical Features
Classic Triad:
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Fever – often low-grade but may be high in acute illness
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Pharyngitis – severe sore throat with tonsillar enlargement, exudates, and petechiae on the palate
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Lymphadenopathy – typically bilateral, cervical (posterior > anterior)
Additional Symptoms:
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Fatigue and malaise (can be prolonged)
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Myalgia
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Headache
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Rash – especially after exposure to aminopenicillins (ampicillin or amoxicillin)
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Hepatosplenomegaly – splenic enlargement in ~50% of patients; mild hepatic transaminase elevation common
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Loss of appetite and nausea
In children – often mild or asymptomatic.
Complications
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Hematologic: Hemolytic anemia, thrombocytopenia, neutropenia
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Neurological: Meningitis, encephalitis, Guillain–Barré syndrome, cranial nerve palsies
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Splenic rupture (rare, but potentially fatal) – usually within the first 3 weeks of illness
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Upper airway obstruction due to tonsillar hypertrophy
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Chronic active EBV infection – rare, severe, persistent illness
Diagnosis
Clinical suspicion: Fever + pharyngitis + lymphadenopathy in a young person, especially with prolonged fatigue.
Laboratory tests:
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Full blood count: Lymphocytosis (>50% lymphocytes, with >10% atypical lymphocytes)
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Liver function tests: Mild–moderate transaminase elevation in most patients
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Heterophile antibody test (Monospot): Positive in ~85% of adolescents/adults after first week; less sensitive in children
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EBV-specific serology:
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Anti-VCA (viral capsid antigen) IgM – acute infection
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Anti-VCA IgG – past or current infection
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Anti-EBNA (nuclear antigen) – appears weeks after infection, indicates past infection
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PCR: Detects EBV DNA in selected cases (immunocompromised patients, atypical presentations)
Differential Diagnosis
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Streptococcal pharyngitis
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Cytomegalovirus mononucleosis
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Acute HIV infection
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Toxoplasmosis
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Viral hepatitis
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Adenovirus infection
Management
There is no specific antiviral therapy for uncomplicated glandular fever – treatment is supportive.
Supportive Measures
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Adequate hydration
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Rest (relative, avoiding strenuous activity until recovery)
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Analgesics/antipyretics:
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Paracetamol (acetaminophen) 500–1000 mg orally every 4–6 hours as needed (max 4 g/day)
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Ibuprofen 400 mg orally every 6–8 hours as needed (max 2.4 g/day)
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Warm saline gargles, lozenges for sore throat
Corticosteroids
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Not routinely indicated in uncomplicated cases
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May be considered for:
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Severe tonsillar hypertrophy with impending airway obstruction
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Massive splenomegaly with risk of rupture
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Severe hemolytic anemia or thrombocytopenia
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Example: Prednisolone 40–60 mg orally daily for 3–5 days, tapered as clinically indicated
Antibiotic Use
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Only if bacterial superinfection (e.g., streptococcal pharyngitis) is confirmed
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Avoid aminopenicillins (ampicillin, amoxicillin) – can trigger widespread maculopapular rash in EBV infection
Activity Restrictions
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Avoid contact sports and heavy lifting for at least 3–4 weeks from onset, or until splenomegaly resolves (to reduce risk of splenic rupture)
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Gradual return to normal activity based on clinical recovery and follow-up assessment
Prognosis
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Most symptoms resolve within 2–4 weeks; fatigue may persist for weeks to months
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Life-threatening complications are rare with appropriate monitoring and supportive care
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Immunity is typically lifelong after infection
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