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Published on: May 27, 2011
Successful cidofovir therapy of progressive multifocal leukoencephalopathy preceding angioimmunoblastic T-cell
Jean-Francois Viallard1, Estibaliz Lazaro, Marie-Edith Lafon
1Service de Médecine Interne et Maladies Infectieuses, Hôpital Haut-Lévâque, 33604 Pessac Cedex, France. jean-francois.viallard@chu-bordeaux.fr
Abstract:
Progressive multifocal leukoencephalopathy (PML) is a subacute demyelinating infectious disease, caused by the human polyomavirus JC (JCV), that usually occurs in immunocompromised patients. In this setting, PML has been observed in increasing numbers of patients with hematological malignancies, mostly lymphoproliferative B-cell disorders. Despite attempts with various drugs, PML has generally remained unresponsive to treatment. We report the successful use of cidofovir in a patient who developed PML 6 months before angioimmunoblastic T-cell lymphoma (AITL) was diagnosed. To the best of our knowledge, this is the first case of PML in AITL. Our case demonstrates the expanding clinical importance of PML in hematological conditions, and neurological symptoms and/or white matter changes on central nervous system imaging should arouse the suspicion of PML and lead to rapid cidofovir introduction. Progressive multifocal leukoencephalopathy (PML) is a subacute demyelinating infectious disease, caused by the human polyomavirus JC (JCV), that usually occurs in immunocompromised patients. In this setting, PML has been observed in increasing numbers of patients with hematological malignancies, mostly lymphoproliferative B-cell disorders. Despite attempts with various drugs, PML has generally remained unresponsive to treatment. We report the successful use of cidofovir in a patient who developed PML 6 months before angioimmunoblastic T-cell lymphoma (AITL) was diagnosed. To the best of our knowledge, this is the first case of PML in AITL. Our case demonstrates the expanding clinical importance of PML in hematological conditions, and neurological symptoms and/or white matter changes on central nervous system imaging should arouse the suspicion of PML and lead to rapid cidofovir introduction.
Insights
Progressive multifocal leukoencephalopathy (PML), a rare brain infection, was successfully treated with cidofovir in a patient with angioimmunoblastic T-cell lymphoma (AITL). This case highlights PML
Area of Science:
- Neurology
- Infectious Diseases
- Hematology
Background:
- Progressive multifocal leukoencephalopathy (PML) is a demyelinating disease caused by JC virus (JCV) in immunocompromised individuals.
- PML incidence is rising in patients with hematological malignancies, particularly B-cell disorders.
- PML has historically shown poor response to available treatments.
Observation:
- A patient developed PML six months prior to the diagnosis of angioimmunoblastic T-cell lymphoma (AITL).
- This represents the first documented case of PML in the context of AITL.
- Neurological symptoms and white matter changes on imaging prompted suspicion of PML.
Findings:
- Successful treatment of PML was achieved using cidofovir.
- Cidofovir demonstrated efficacy in a patient with PML and AITL.
- The treatment course suggests cidofovir as a viable therapeutic option.
Implications:
- PML is an increasingly recognized complication in hematological conditions beyond B-cell disorders.
- Early suspicion and diagnosis of PML are crucial for timely intervention.
- Cidofovir offers a promising treatment avenue for PML in immunocompromised patients, including those with AITL.
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