🦠 Cytomegalovirus (CMV) is a member of the Herpesviridae family.
It often mimics EBV and toxoplasmosis clinically but is usually asymptomatic in immunocompetent hosts.
⚠️ In pregnancy and in immunocompromised patients, CMV can be severe and life-threatening.
📖 About
- Very common virus – >50% of adults are seropositive.
- Peak infection around age 30.
- Latency in monocytes and reactivation in immunosuppression.
- Most healthy people have mild or no symptoms.
🧬 Aetiology
- Double-stranded DNA virus in the Herpesviridae family.
- Found in saliva, urine, semen, breast milk, blood, cervical/vaginal secretions.
- Transmission via close contact, transfusion, transplant, vertical (transplacental).
⚠️ Clinical Features
- Asymptomatic in most healthy individuals.
- Mononucleosis-like illness:
- Malaise, headache, pharyngitis, cervical lymphadenopathy.
- Distinguishing feature: Monospot negative.
Complications (rare): Guillain-Barré syndrome, meningoencephalitis, myocarditis, pericarditis.
Other features: Thrombocytopenia, autoimmune haemolytic anaemia, maculopapular rash (esp. after ampicillin), hepatomegaly ± mild hepatitis.
🧑⚕️ In Immunocompromised (esp. CD4 < 50)
- CMV pneumonitis, encephalitis, hepatitis, retinitis (“pizza pie retinopathy”).
- Colitis and oesophagitis – causes bloody diarrhoea, abdominal pain.
- Pancreatitis, adrenalitis → diabetes/adrenal dysfunction.
- Monitor with CMV DNA PCR viral load.
🤰 In Pregnancy (Congenital CMV)
- Occurs in ~1 in 800 pregnancies.
- Features: IUGR, hepatosplenomegaly, jaundice, thrombocytopenia.
- Severe: Microcephaly, periventricular calcifications, chorioretinitis, deafness, seizures.
- Leading infectious cause of congenital sensorineural hearing loss.
🔬 Investigations
- Bloods: Atypical lymphocytosis.
- Monospot: Negative (helps differentiate from EBV).
- Histology: “Owl’s eye” intranuclear inclusions.
- Serology: CMV IgM (recent infection), rising IgG titres.
- PCR: Detects CMV DNA – used in transplant and HIV patients for monitoring.
- Other labs: ↑ LFTs, ↑ amylase (if pancreatitis), cytopenias.
💊 Management
- Immunocompetent: Usually supportive only.
- Severe / immunocompromised / congenital CMV:
- IV Ganciclovir 5 mg/kg 12-hourly.
- Oral Valganciclovir (prodrug, better bioavailability) 900 mg BD × 14 days.
- Foscarnet or Cidofovir if ganciclovir-resistant.
- Monitor viral load by PCR to assess treatment response.
- Side-effects: neutropenia, thrombocytopenia, renal toxicity, male infertility.
📌 Key Exam Tips
- CMV vs EBV: Both give “mono-like” picture, but EBV Monospot +ve / CMV Monospot –ve.
- CMV retinitis is an AIDS-defining illness (CD4 < 50).
- “Owl’s eye” inclusion is the buzzword histology finding.
- Congenital CMV → think microcephaly + periventricular calcifications.
Cases — Cytomegalovirus (CMV) Infection
- Case 1 — Primary CMV in Immunocompetent Adult:
A 25-year-old man presents with 2 weeks of fever, malaise, sore throat, and lymphadenopathy. Monospot test for EBV is negative. LFTs mildly elevated. CMV IgM positive, IgG negative.
Diagnosis: Primary CMV mononucleosis-like illness.
Management: Supportive (fluids, rest, analgesia); antivirals not usually required in immunocompetent patients.
- Case 2 — CMV in Immunocompromised (Renal Transplant):
A 50-year-old renal transplant recipient on immunosuppressants develops fever, diarrhoea, and abdominal pain. Colonoscopy: colitis with ulcerations. Biopsy shows CMV inclusions.
Diagnosis: CMV colitis in immunosuppressed patient.
Management: IV ganciclovir (or oral valganciclovir if mild), reduction of immunosuppression if possible.
- Case 3 — Congenital CMV Infection:
A newborn girl is small for gestational age, with petechiae, hepatosplenomegaly, and microcephaly. Cranial ultrasound: periventricular calcifications. Maternal history: flu-like illness at 10 weeks’ gestation.
Diagnosis: Congenital CMV infection.
Management: Antivirals (valganciclovir) in symptomatic neonates; supportive therapy for complications (hearing loss, developmental delay).
Teaching Commentary 🦠
CMV is a ubiquitous herpesvirus, usually asymptomatic but with key clinical syndromes:
- Primary CMV: mononucleosis-like, heterophile antibody negative.
- Immunocompromised: severe end-organ disease (colitis, pneumonitis, retinitis).
- Congenital CMV: leading cause of non-genetic sensorineural hearing loss and neurodevelopmental delay.
Diagnosis: CMV IgM/IgG serology, PCR, or tissue histology with “owl’s eye” inclusions.
Treatment: usually supportive in immunocompetent; ganciclovir/valganciclovir in severe or immunocompromised disease.