Mononucleosis Flashcards
General findings
Measles-like exanthem dopo 5-9 giorni dalla somministrazione💥
NB Atraumatic splenic rupture due to splenomegaly (spesso infatti si procede con splenectomia profilattica)
Infectious mononucleosis (IM), also called “mono” or the “kissing disease”, is an acute condition caused by the Epstein-Barr virus (EBV). The disease is highly contagious and spreads via bodily secretions, especially saliva. Infection frequently goes unnoticed in children; mainly adolescents and young adults exhibit symptoms. Symptomatic individuals typically first experience fever, malaise, and fatigue, which is later accompanied by acute pharyngitis, tonsillitis, lymphadenopathy, and/or splenomegaly lasting up to a month. IM is also sometimes associated with a measles-like exanthem, especially in individuals who are falsely diagnosed with bacterial tonsillitis and given ampicillin or amoxicillin. To avoid misdiagnosis, suspected cases are confirmed with a heterophile antibody test (monospot test), or in some cases, positive serology. Patients exhibit lymphocytosis, often with atypical T lymphocytes on a peripheral smear. IM is treated symptomatically, as it is usually self-limiting.
Although complications are rare, IM is associated with atraumatic splenic rupture due to splenomegaly and multiple malignancies (e.g., Hodgkin’s lymphoma, Burkitt lymphoma).
Epidemiology
- Approx. 90–95% of adults are EBV-seropositive worldwide.
- Peak incidence of symptomatic disease: 15–24 years
Etiology
- Pathogen: Epstein-Barr virus (EBV), also called human herpes virus 4 (HHV-4) (il virus della varicella invece può anche essere definito HHV-3)
- Transmission: Infectious mononucleosis is highly contagious and spreads via bodily secretions, especially saliva → “kissing disease” (Transmission can occur up to several weeks after the onset of symptoms.)
Fisiopatologia
👓CD21!! I linfociti colpiti sono di tipo B! attenzione
Linfociti atipici allo striscio di sangue!
Linfociti T CD8 che attaccano i linfociti B infetti
EBV infects B lymphocytes in mucosal epithelium (e.g., oropharynx, cervix) via the CD21 receptor → infected B lymphocytes induce a humoral (B-cell) as well as a cellular (T-cell) immune response → an increased concentration of atypical lymphocytes in the bloodstream, which are CD8+ cytotoxic T cells that fight infected B lymphocytes
Clinica
Young children are often asymptomatic.
FARINGITE-TONSILLITE-ADENOPATIA CERVICALE/DIFFFUSA (ddx con fase acuta HIV infection)
- Incubation period: 4–8 weeks💥
- Symptoms typically occur in adolescents and young adults and last for 2–4 weeks.
- Splenomegaly (50% of cases), fever, fatigue, malaise
- Pharyngitis and/or tonsillitis (reddened, enlarged tonsils covered in pus); palatal petechiae
- Bilateral cervical lymphadenopathy (especially posterior) that may become generalized and can, in severe cases, lead to airway obstruction
- Abdominal pain
- Possibly hepatomegaly and jaundice (EPATITE)
✔Maculopapular rash (similar to measles): caused by the infection itself in about 5% of cases, but is generally associated with the administration of aminopenicillin (e.g., ampicillin or amoxicillin) (The rate of aminopenicillin-related exanthem is very high (roughly around 50%) and is assumed to be due to antibodies against aminopenicillins. It is not caused by an allergic drug reaction. Non è una reazione allergica al farmaco!!)
Diagnosis
- Monospot test: detects heterophile antibodies produced in response to EBV infection using RBCs from horses; specificity of ∼ 100%, sensitivity of 85%
- Laboratory analysis: elevated LDH and liver transaminases
- Peripheral smear: lymphocytosis with > 10% atypical lymphocytes (in some cases, up to 90%) 💥 ( Despite being activated T cells, atypical lymphocytes strongly resemble monocytes in terms of their appearance, hence the name infectious mononucleosis.)
Serology: indicated if IM is suspected but a monospot test is negative
-Anti-viral capsid antigen antibodies (anti-VCA)
-Anti-VCA IgM: appears early and vanishes ∼ 3
months after infection
-Anti-VCA IgG: appears after 2–4 weeks and persists
for life
Histopathology of lymph nodes
- Reactive follicular hyperplasia due to increased activation of B lymphocytes
- Paracortical expansion through numerous, large immunoblasts (B and T cells), later expanding throughout the entire node
- Atypical Reed-Sternberg-like cells may be observed, which is why the disease is sometimes mistaken for Hodgkin’s disease.
Treatment
✔Symptomatic therapy
- Avoid physical activity that may trigger splenic rupture (e.g., contact sports) for at least 3 weeks after the onset of symptoms.
- Fluids (IV administration if necessary)
- Analgesics/antipyretics (e.g., acetaminophen)
Complications
- Guillame-Barrè
- linfoma di Burkitt
- splenic rupture