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Infectious Mononucleosis Clinical Presentation

  • Author: Burke A Cunha, MD; Chief Editor: Michael Stuart Bronze, MD  more...
Updated: Oct 06, 2015


See the list below:

  • Most patients with Epstein-Barr virus (EBV) infectious mononucleosis are asymptomatic and, therefore, have few if any symptoms. Most adults (approximately 90%) show serological evidence of previous EBV infection.
  • The incubation period of EBV infectious mononucleosis is 1-2 months. Many patients cannot recall close contact with individuals with pharyngitis. Virtually all patients with EBV infectious mononucleosis report fatigue and prolonged malaise. A sore throat is second only to fatigue and malaise as a presenting symptom.
  • Fever is usually present and is low grade, but chills are relatively uncommon. Arthralgias and myalgias occur but are less common than in other viral infectious diseases.
  • Nausea and anorexia, without vomiting, are common symptoms.
  • Various other symptoms have been described in patients with EBV infectious mononucleosis, including cough, ocular muscle pain, chest pain, and photophobia.
  • Importantly, patients without CNS involvement experience no cognitive difficulties. CMV infectious mononucleosis rarely involves the CNS.
  • Myalgias, which are uncommon, are rarely (if ever) severe.


See the list below:

  • Physical findings in infectious mononucleosis should be viewed in terms of frequency distribution and time course after clinical presentation.
  • Early signs include fever, lymphadenopathy, pharyngitis, rash, and/or periorbital edema. Relative bradycardia has been described in some patients with EBV mononucleosis, but it is not a constant finding.
  • Later physical findings include hepatomegaly, palatal petechiae, jaundice, uvular edema, splenomegaly, and, rarely (1-2%), findings associated with splenic rupture.
  • CNS findings associated with EBV mononucleosis are rare but usually occur later in the course of the illness.
  • Splenic tenderness may be present in patients with splenomegaly.
  • Pulmonary involvement is not a feature of EBV infectious mononucleosis.
  • The classic presentation of EBV infectious mononucleosis in children and young adults consists of the triad of fever, pharyngitis, and lymphadenopathy.
  • Older adults and elderly patients with EBV infectious mononucleosis often have few signs and symptoms referable to the oropharynx and have little or no adenopathy. Elderly patients with EBV mononucleosis present clinically as having anicteric viral hepatitis.
  • Predictably, jaundice develops in less than 10% of young adults with EBV infectious mononucleosis, but jaundice may occur in as many as 30% of affected elderly individuals.
  • The pharyngitis due to EBV infectious mononucleosis may be exudative or nonexudative.
    • Exudative pharyngitis is commonly confused with group A streptococcal pharyngitis, which is complicated further by the fact that approximately 30% of patients with EBV infectious mononucleosis have group A streptococcal carriage of the oropharynx. The unwary physician may incorrectly conclude that a throat culture or rapid test positive for group A streptococci in a patient with infectious mononucleosis represents streptococcal pharyngitis.
    • Nonexudative pharyngitis with or without tonsillar enlargement is common in patients with EBV infectious mononucleosis and resembles viral pharyngitis.
    • Patients with either exudative or nonexudative EBV infectious mononucleosis are commonly colonized by group A streptococci.
  • Tonsillar enlargement is common, and massive tonsillar enlargement may be observed. The term kissing tonsils is used to describe extreme enlargement of both tonsils in patients with EBV infectious mononucleosis. Extreme tonsillar enlargement may result in airway obstruction.
  • Palatal petechiae of the posterior oropharynx distinguish infectious mononucleosis from other causes of viral pharyngitis but do not distinguish it from group A streptococcal pharyngitis, in which palatal petechiae may occur.
  • Uvular edema is an uncommon finding in infectious mononucleosis, but, if present, it is a helpful sign in distinguishing EBV infectious mononucleosis from other causes of viral pharyngitis or from group A streptococcal pharyngitis.
  • Early in the course of EBV infectious mononucleosis, patients may present with a maculopapular generalized rash. The rash is faint and evanescent and rapidly disappears. It is nonpruritic. This is a marked contrast to patients mistakenly diagnosed with streptococcal pharyngitis who have been administered ampicillin or amoxicillin and then develop a maculopapular rash as a drug reaction. Drug-induced rash is usually pruritic and is prolonged, in contrast to the viral rash of EBV infectious mononucleosis. Patients with EBV infectious mononucleosis who experience drug reactions to beta-lactams are not allergic to these medications. Administration of beta-lactams after resolution of the infection does not result in drug fevers or rashes.
  • Splenomegaly is a late finding in EBV infectious mononucleosis. Splenic enlargement returns to normal or near normal usually within 3 weeks after the clinical presentation.
  • In rare cases, EBV infectious mononucleosis results in various unusual clinical manifestations, including encephalitis, pancreatitis, acalculous cholecystitis, myocarditis, mesenteric adenitis, myositis, and glomerular nephritis.
  • Neurologic syndromes due to EBV infectious mononucleosis include optic neuritis, transverse myelitis, aseptic meningitis, encephalitis, meningoencephalitis, cranial nerve (CN) palsies (particularly CN VII), and Guillain-Barré syndrome.
  • Although EBV-induced antibodies to RBC membranes may occur, clinical anemia is uncommon with EBV infectious mononucleosis.
  • Leukocytosis, rather than leukopenia, is the rule in infectious mononucleosis.
  • Periorbital edema is an uncommon, and therefore fairly specific, physical finding in infectious diseases.
    • Bilateral periorbital edema not associated with generalized edema (eg, nephrotic syndrome) suggests trichinosis, Kawasaki disease, allergic reactions, or bilateral periorbital cellulitis.
    • Unilateral periorbital edema suggests conditions such as thyrotoxicosis, retro-orbital eye tumor, Chagas disease, insect sting, or unilateral conjunctivitis.
    • EBV infectious mononucleosis is characterized by early and transient bilateral upper-lid edema. In contrast to the disorders mentioned above, which are either unilateral or bilateral and involve the periorbital area, with or without the eyelids, the external eye involvement of EBV infectious mononucleosis is characterized by bilateral upper-lid edema. This finding was first described by Hoagland and is referred to as Hoagland sign. Hoagland noted the association of EBV infectious mononucleosis in young military recruits with EBV infectious mononucleosis. Hoagland sign may be detected when patients look in the mirror early in the course of their illness or when the astute physician notices this early in the clinical presentation. Hoagland sign is present for only the first few days of illness and should not be sought later in the course of the infectious process.

Table 1. Differential Diagnoses of Infectious Mononucleosis (Open Table in a new window)

Clinical Parameters Epstein-Barr Virus Cyto-megalovirusToxoplasmosisViral Hepatitis
Mild sore throat+++/-+/-
Early maculopapular rash±--+/-
SignsEarly bilateral upper eyelid edema±---
Unilateral localized adenopathy--+-
Bilateral posterior cervical adenopathy++-+/-
Tender hepatomegaly+/-+/--+
Laboratory abnormalitiesWBC countN*/-N/-N¯
Elevated SGOT/SGPT++++/-+++
Atypical lymphocytes (≥ 10%)++--
Elevated IgM§ CMV titer-+--
Elevated IgM EBV VCAII titer+---
Elevated IgM toxoplasmosis titer--+-
Positive hepatitis (eg, A, B, D) test---+

Serum glutamic-oxaloacetic transaminase

Serum glutamic-pyruvic transaminase

§ Immunoglobulin M

II Viral capsid antigen



See the list below:

  • The only predisposing risk factor for EBV infectious mononucleosis is close contact with an individual infected with EBV.
  • EBV commonly persists in oropharyngeal secretions for months after clinical resolution of EBV infectious mononucleosis.
  • Patients with congenital immunodeficiencies are predisposed to EBV-induced lymphoproliferative disorders and malignancies.
  • Acquired immunodeficiencies due to the effects of immunosuppression (eg, PLDT) or infectious disease-induced immunosuppression (ie, HIV) may predispose to oral hairy leukoplakia or non-Hodgkin lymphoma.
  • Burkitt lymphoma has a distribution (ie, in Africa) that is the same as the distribution of malaria. The geographic location predisposes to Burkitt lymphoma in children.
Contributor Information and Disclosures

Burke A Cunha, MD Professor of Medicine, State University of New York School of Medicine at Stony Brook; Chief, Infectious Disease Division, Winthrop-University Hospital

Burke A Cunha, MD is a member of the following medical societies: American College of Chest Physicians, American College of Physicians, Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Specialty Editor Board

Francisco Talavera, PharmD, PhD Adjunct Assistant Professor, University of Nebraska Medical Center College of Pharmacy; Editor-in-Chief, Medscape Drug Reference

Disclosure: Received salary from Medscape for employment. for: Medscape.

John W King, MD Professor of Medicine, Chief, Section of Infectious Diseases, Director, Viral Therapeutics Clinics for Hepatitis, Louisiana State University Health Sciences Center; Consultant in Infectious Diseases, Overton Brooks Veterans Affairs Medical Center

John W King, MD is a member of the following medical societies: American Association for the Advancement of Science, American College of Physicians, American Federation for Medical Research, Association of Subspecialty Professors, American Society for Microbiology, Infectious Diseases Society of America, Sigma Xi

Disclosure: Nothing to disclose.

Chief Editor

Michael Stuart Bronze, MD David Ross Boyd Professor and Chairman, Department of Medicine, Stewart G Wolf Endowed Chair in Internal Medicine, Department of Medicine, University of Oklahoma Health Science Center; Master of the American College of Physicians; Fellow, Infectious Diseases Society of America

Michael Stuart Bronze, MD is a member of the following medical societies: Alpha Omega Alpha, American Medical Association, Oklahoma State Medical Association, Southern Society for Clinical Investigation, Association of Professors of Medicine, American College of Physicians, Infectious Diseases Society of America

Disclosure: Nothing to disclose.

Additional Contributors

Charles S Levy, MD Associate Professor, Department of Medicine, Section of Infectious Disease, George Washington University School of Medicine

Charles S Levy, MD is a member of the following medical societies: American College of Physicians, Infectious Diseases Society of America, Medical Society of the District of Columbia

Disclosure: Nothing to disclose.

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Table 1. Differential Diagnoses of Infectious Mononucleosis
Clinical Parameters Epstein-Barr Virus Cyto-megalovirusToxoplasmosisViral Hepatitis
Mild sore throat+++/-+/-
Early maculopapular rash±--+/-
SignsEarly bilateral upper eyelid edema±---
Unilateral localized adenopathy--+-
Bilateral posterior cervical adenopathy++-+/-
Tender hepatomegaly+/-+/--+
Laboratory abnormalitiesWBC countN*/-N/-N¯
Elevated SGOT/SGPT++++/-+++
Atypical lymphocytes (≥ 10%)++--
Elevated IgM§ CMV titer-+--
Elevated IgM EBV VCAII titer+---
Elevated IgM toxoplasmosis titer--+-
Positive hepatitis (eg, A, B, D) test---+

Serum glutamic-oxaloacetic transaminase

Serum glutamic-pyruvic transaminase

§ Immunoglobulin M

II Viral capsid antigen

Table 2. EBV Serologic Responses in EBV-Associated Diseases
EBV DiseasesEBV Antibody Responses



IgMIgGDiffuse EARestricted EAAnti-EBNA
Acute EBV mononucleosis++++--
Past EBV infection--+--+
Chronic active EBV infection--++++++
Burkitt lymphoma--++++/-++
Nasopharyngeal carcinoma--+++++/-+
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