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๐ก 90% of patients with Infectious Mononucleosis develop a rash if given ampicillin or amoxicillin โ a classic diagnostic clue.
๐ About
- One of the main causes of Infectious Mononucleosis (Glandular Fever).
- Very common infection โ 90% of adults show past EBV exposure.
- Clinical picture can mimic CMV or Toxoplasmosis โ always check, especially in pregnancy or immunocompromised.
๐ฆ Virology
- EBV = a gamma herpesvirus.
- Spread via saliva droplets โ classically โthe kissing diseaseโ ๐.
- Often subclinical in childhood; symptomatic illness more likely in adolescents/young adults.
- 50% of infections cause clinical symptoms.
- Not highly contagious โ isolation not required.
๐ฉบ Clinical Features
- Often subclinical.
- Non-specific flu-like illness: headache, malaise, fever ๐ค.
- Severe sore throat + tonsillar enlargement.
- Generalised tender lymphadenopathy (cervical, axillary, inguinal).
- Hepatitis โ jaundice, raised LFTs.
- Splenomegaly (โ ๏ธ risk of rupture).
- Skin features: erythema multiforme, petechiae, periorbital oedema.
- Rare CNS: encephalitis, meningitis. Disease severity โ with age.
๐คฐ Pregnancy
- If heterophile antibodies negative โ check CMV serology.
- CMV can mimic EBV, but active CMV in pregnancy can cause congenital abnormalities.
- Toxoplasmosis also mimics โ must exclude.
๐ Causes of Infectious Mononucleosis-like Syndrome
- Epstein-Barr virus (EBV)
- Cytomegalovirus (CMV)
- Human Herpesvirus-6 (HHV-6)
- HIV seroconversion
- Toxoplasmosis
โ ๏ธ Long-Term Complications
- Nasopharyngeal carcinoma ๐ญ
- Burkittโs lymphoma
- Post-transplant lymphoproliferative disease
- HIV-related immunoblastic lymphoma
- Chronic fatigue syndrome
- Duncanโs syndrome (X-linked lymphoproliferative syndrome due to SAP gene mutation)
๐ Differentials
- Streptococcal sore throat (no hepatosplenomegaly or atypical lymphocytes).
- CMV infection.
- Toxoplasmosis.
- Viral hepatitis.
- HIV seroconversion.
- Lymphoma / Leukaemia.
๐งช Investigations
- FBC: mononuclear lymphocytosis with atypical lymphocytes, neutropenia, thrombocytopenia.
- LFT: raised ALT, raised bilirubin.
- Atypical CD8+ T lymphocytes โ can mimic acute leukaemia.
- Monospot (Paul-Bunnell test): detects heterophile antibodies. Positive in week 2, may need repeat if negative initially.
- EBV serology: IgM EBV EA (early antigen) + negative IgG EBV confirms acute infection.
- Viral PCR (if needed).
๐ Causes of Atypical Lymphocytosis
- EBV
- HIV seroconversion
- Viral hepatitis
- Mumps
- Rubella
๐ Management
- Supportive: rest, fluids, paracetamol/NSAIDs. Fatigue may last 6 weeks.
- โ ๏ธ Avoid ampicillin/amoxicillin โ rash in 90% of cases.
- Advise against contact sports until splenomegaly resolves (risk of rupture).
- For airway compromise / severe pharyngeal oedema โ prednisolone 30โ60 mg OD ร 5 days.
- Treat streptococcal superinfection with IV benzylpenicillin or erythromycin (not amoxicillin).
- No role for antivirals against EBV.
๐ Key Exam Pearls
- Ampicillin rash = diagnostic clue ๐ฏ.
- Splenomegaly โ avoid contact sports.
- Monospot test = heterophile antibodies (Paul-Bunnell).
- Consider CMV/toxoplasmosis in pregnancy.
Cases - EpsteinโBarr Virus (EBV) Infection
- Case 1 - Infectious Mononucleosis (Glandular Fever):
An 18-year-old university student presents with sore throat, fever, malaise, and cervical lymphadenopathy. Exam: tonsillar enlargement with exudates, splenomegaly. Bloods: lymphocytosis with atypical lymphocytes. Monospot test positive.
Diagnosis: EBV infectious mononucleosis.
Management: Supportive (hydration, rest, paracetamol/NSAIDs). Avoid amoxicillin (rash risk) and contact sports for 4 weeks due to splenic rupture risk.
- Case 2 - EBV-Associated Malignancy (Burkitt Lymphoma):
A 9-year-old boy from East Africa presents with a rapidly enlarging jaw mass. Biopsy shows โstarry skyโ appearance with medium-sized B-cells. EBV DNA detected in tumour tissue.
Diagnosis: EBV-associated endemic Burkitt lymphoma.
Management: Intensive multi-agent chemotherapy; supportive care; oncology referral.
- Case 3 - EBV-Driven Lymphoproliferation in Immunosuppressed Host:
A 45-year-old renal transplant patient on immunosuppressants develops fever, night sweats, weight loss, and lymphadenopathy. Lymph node biopsy shows EBV-positive B-cell proliferation consistent with post-transplant lymphoproliferative disorder (PTLD).
Diagnosis: EBV-associated PTLD.
Management: Reduction of immunosuppression, rituximab-based therapy, possible chemotherapy in refractory cases.
Teaching Commentary ๐งพ
EBV is a gamma-herpesvirus transmitted via saliva (โkissing diseaseโ). Primary infection in adolescents/young adults โ infectious mononucleosis. Complications: splenic rupture, hepatitis, haemolytic anaemia. EBV is oncogenic, associated with Burkitt lymphoma, Hodgkin lymphoma, nasopharyngeal carcinoma, and PTLD.
Diagnosis: heterophile antibody test (Monospot), EBV-specific serology, PCR.
Treatment: usually supportive, except in EBV-driven malignancies or PTLD where chemotherapy, immunotherapy, or reduction of immunosuppression is required.