Epstein–Barr virus (EBV) infection commonly presents as infectious mononucleosis with fever, pharyngitis, and lymphadenopathy. Periorbital edema, known as Hoagland sign, is a relatively specific clinical sign of EBV infection and may precede other classical findings. Neurological manifestations are uncommon in children. We report a previously healthy 10-year-old boy who presented with fever, severe sore throat, cervical lymphadenopathy, and bilateral partial ptosis consistent with Hoagland sign. Laboratory investigations showed leukocytosis with lymphocytic predominance and significant atypical lymphocytosis, along with elevated transaminases. EBV PCR was positive. The patient recovered fully with supportive care. This case highlights Hoagland sign as an important early diagnostic clue in EBV infection
Introduction
Epstein–Barr virus is a ubiquitous herpesvirus
responsible for infectious mononucleosis, particularly in school-aged children
and adolescents [1]. The classic triad includes fever, pharyngitis, and
lymphadenopathy. Laboratory findings typically reveal lymphocytosis with
atypical lymphocytes and mild elevation of liver enzymes [2]. Hoagland first
described periorbital edema associated with infectious mononucleosis, now
referred to as Hoagland sign, which is considered relatively specific for EBV
infection [3]. Although neurological complications occur in 1–5% of cases,
isolated bilateral ptosis is rarely reported in children [4].
Case
Presentation
A previously well 10-year-old boy presented with a
two-day history of fever (maximum 99.9°F) and severe sore throat with coryzal
symptoms. There was no significant contact history. Examination revealed
bilateral enlarged tonsils with pustular exudates and significant bilateral
submandibular cervical lymphadenopathy. Notably, bilateral partial ptosis was
observed, consistent with Hoagland sign (Figures 1–3). Extraocular movements
were intact, pupils were equal and reactive, and no other focal neurological deficits
were detected. Abdominal examination was normal with no hepatosplenomegaly.
Laboratory investigations demonstrated leukocytosis
(24,000/µL) with 75% lymphocytes. Peripheral blood film showed a significant
number of atypical lymphocytes. Hemoglobin was 12.5 g/dL and platelet count
193,000/µL. Inflammatory markers showed ESR 24 mm/hr and CRP 32 mg/L. Liver
function tests revealed elevated AST (134 U/L) and ALT (195 U/L). Renal
function was normal. Throat swab culture was negative for bacterial organisms.
Ultrasound abdomen showed no hepatosplenomegaly. EBV PCR returned positive, confirming
acute EBV infection.
The patient was initially managed with intravenous
ceftriaxone for five days and intravenous dexamethasone for four days due to
significant tonsillar inflammation. Antibiotics were completed for ten days and
transitioned to oral co-amoxiclav. No antibiotic-associated rash developed.
Clinical improvement was observed within several days, and complete resolution
of fever, lymphadenopathy, and ptosis occurred within two weeks.
Figure 1: Frontal view demonstrating bilateral partial ptosis (Hoagland sign)
Figure 2: Right lateral view showing upper eyelid drooping
Figure 3: Left lateral view confirming bilateral involvement
Discussion
Infectious mononucleosis is most frequently caused by
EBV and presents with characteristic systemic findings [1,2]. Hoagland sign
refers to transient bilateral upper eyelid edema and ptosis observed in the
early phase of EBV infection [3]. It is thought to result from lymphatic
obstruction and inflammatory infiltration of periorbital tissues. The presence
of Hoagland sign may serve as a valuable early diagnostic clue before
serological confirmation.
Neurological manifestations of EBV are uncommon but
include meningitis, encephalitis, cranial nerve palsies, and peripheral
neuropathies [4]. In this case, preserved pupillary reflexes and ocular
motility suggest partial cranial nerve involvement or localized inflammatory
edema rather than complete third nerve palsy. The rapid and complete recovery
supports a transient immune-mediated mechanism
Conclusion
This case highlights Hoagland sign as a relatively
specific and under-recognized clinical sign of EBV infection in children. The
presence of atypical lymphocytosis further strengthens the diagnosis.
Recognition of this feature may facilitate early diagnosis and avoid
unnecessary investigations. The prognosis is favorable, with spontaneous
resolution in most cases.
Ethical
Statement
Written informed consent was obtained from the
patient’s parents for publication of this case report and accompanying clinical
photographs. All identifying information has been anonymized to protect patient
confidentiality.
References