Cauda equina syndrome in a patient with human immunodeficiency virus and secondary central nervous system lymphoma: a case report.


Journal

Journal of medical case reports
ISSN: 1752-1947
Titre abrégé: J Med Case Rep
Pays: England
ID NLM: 101293382

Informations de publication

Date de publication:
15 Nov 2023
Historique:
received: 27 07 2023
accepted: 12 10 2023
medline: 16 11 2023
pubmed: 15 11 2023
entrez: 15 11 2023
Statut: epublish

Résumé

Secondary central nervous system lymphoma (SCNSL) is a known complication of immunocompromised patients with most cases involving the brain parenchyma. Reports of cauda equina syndrome (CES) caused by SCNSL are exceedingly scarce as involvement of this anatomical region is extremely uncommon. We report a case of a 46-years-old, African, female patient with human immunodeficiency virus (HIV) who developed CES in the context of SCNSL. There were no blasts present in the peripheral blood smear. We provide a review of the literature, discussion of the clinical evolution of this patient and the radiological/histopathological findings. The patient ultimately responded well to induction chemotherapy and high dose methotrexate. This case report demonstrates that CES, while a rare occurrence in this clinical context, should be considered in at-risk patients especially those presenting with abnormal neurological findings. Prompt recognition may prevent permanent neurological injury and obviate the need for more invasive therapeutic interventions.

Sections du résumé

BACKGROUND BACKGROUND
Secondary central nervous system lymphoma (SCNSL) is a known complication of immunocompromised patients with most cases involving the brain parenchyma. Reports of cauda equina syndrome (CES) caused by SCNSL are exceedingly scarce as involvement of this anatomical region is extremely uncommon.
CASE PRESENTATION METHODS
We report a case of a 46-years-old, African, female patient with human immunodeficiency virus (HIV) who developed CES in the context of SCNSL. There were no blasts present in the peripheral blood smear. We provide a review of the literature, discussion of the clinical evolution of this patient and the radiological/histopathological findings. The patient ultimately responded well to induction chemotherapy and high dose methotrexate.
CONCLUSION CONCLUSIONS
This case report demonstrates that CES, while a rare occurrence in this clinical context, should be considered in at-risk patients especially those presenting with abnormal neurological findings. Prompt recognition may prevent permanent neurological injury and obviate the need for more invasive therapeutic interventions.

Identifiants

pubmed: 37964357
doi: 10.1186/s13256-023-04212-5
pii: 10.1186/s13256-023-04212-5
pmc: PMC10647035
doi:

Types de publication

Review Case Reports Journal Article

Langues

eng

Sous-ensembles de citation

IM

Pagination

476

Informations de copyright

© 2023. The Author(s).

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Auteurs

Alexander Tang (A)

Division of General Internal Medicine, McGill University Health Centre, Montreal, Canada. alexander.tang@mail.mcgill.ca.

David Di Fonzo (D)

Division of General Internal Medicine, McGill University Health Centre, Montreal, Canada.

Mohammed Redha (M)

Division of General Internal Medicine, McGill University Health Centre, Montreal, Canada.

Michael Churchill-Smith (M)

Division of General Internal Medicine, McGill University Health Centre, Montreal, Canada.

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Classifications MeSH