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Subacute measles encephalitis with AIDS diagnosed by fine needle aspiration biopsy. A case report
T P Poon1, V Tchertkoff, H Win
1Department of Pathology, New York Medical College, Metropolitan Hospital Center, New York 10029, USA.
Background:
Subacute measles encephalitis (SME), or measles inclusion body encephalitis (MIBE), is a rare central nervous system (CNS) complication following infection by the measles (rubeola) virus. It usually occurs in young patients with defective cellular immunity from either congenital or acquired causes. In the United States, with the resurgence of measles infection and the human immunodeficiency virus (HIV) pandemic, subacute measles encephalitis should be added to the differential diagnosis in acquired immune deficiency syndrome (AIDS) patients presenting with unexplained CNS manifestations.
Case:
A 2-year-old, HIV-positive, white male was admitted for generalized convulsive seizures. Vaccination was described as "up to date." Despite treatment with anticonvulsive drugs, the child continued to develop frequent partial and generalized seizures. Cephalic computed tomography and magnetic resonance imaging revealed a hypodense area in the right parietotemporal cortex without an associated mass effect. Fine needle aspiration biopsy (FNAB) of the affected area showed neuronal reduction, degeneration with eosinophilic intranuclear inclusions, perivascular lymphoplasmacytic infiltration and gliosis. Electron microscopy of the intranuclear inclusions revealed fine, fibrillar, tubular nucleocapsids, consistent with the measles virus.
Conclusion:
Acute measles encephalitis (AME), subacute sclerosing panencephalitis (SSPE), and SME are the three CNS syndromes associated with measles infection. Serum and cerebrospinal fluid (CSF) antibody titres against measles virus are usually high and helpful in the diagnosis of AME and SSPE. In SME, neither serum nor CSF antibody titres against measles are high. Therefore, FNAB is necessary for a definitive diagnosis.
Insights
Subacute measles encephalitis (SME) is a rare CNS complication in immunocompromised patients. Diagnosis requires brain biopsy, as antibody titers are not elevated, unlike other measles-related syndromes.
Area of Science:
- Neurology
- Infectious Diseases
- Virology
Background:
- Subacute measles encephalitis (SME), also known as measles inclusion body encephalitis (MIBE), is a rare central nervous system (CNS) complication of measles virus infection.
- It predominantly affects young individuals with compromised cellular immunity, whether congenital or acquired.
- With measles resurgence and the HIV pandemic, SME should be considered in acquired immune deficiency syndrome (AIDS) patients with unexplained CNS symptoms.
Observation:
- A 2-year-old, HIV-positive male presented with refractory seizures.
- Neuroimaging revealed a hypodense lesion in the right parietotemporal cortex.
- Brain biopsy showed characteristic eosinophilic intranuclear inclusions and viral nucleocapsids on electron microscopy.
Findings:
- The patient's presentation and biopsy results confirmed measles inclusion body encephalitis (MIBE).
- Unlike acute measles encephalitis (AME) and subacute sclerosing panencephalitis (SSPE), SME does not typically show elevated serum or cerebrospinal fluid (CSF) measles antibody titers.
- Fine needle aspiration biopsy (FNAB) proved essential for definitive diagnosis.
Implications:
- This case highlights the importance of considering SME in the differential diagnosis of CNS disorders in immunocompromised individuals, particularly those with HIV.
- Diagnostic strategies for SME must account for the absence of elevated antibody titers.
- FNAB is a critical diagnostic tool for confirming SME when serological tests are inconclusive.
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