Skip to main page content
U.S. flag

An official website of the United States government

Dot gov

The .gov means it’s official.
Federal government websites often end in .gov or .mil. Before sharing sensitive information, make sure you’re on a federal government site.

Https

The site is secure.
The https:// ensures that you are connecting to the official website and that any information you provide is encrypted and transmitted securely.

Access keys NCBI Homepage MyNCBI Homepage Main Content Main Navigation
Review
. 2009 Nov 15;34(24):E882-5.
doi: 10.1097/BRS.0b013e3181b29de6.

Primary NK/T-cell lymphoma of the cauda equina: a case report and literature review

Affiliations
Review

Primary NK/T-cell lymphoma of the cauda equina: a case report and literature review

Masahiro Morita et al. Spine (Phila Pa 1976). .

Abstract

Study design: A case report with a review of the literature.

Objective: To describe an unusual case of primary lymphoma of the cauda equina and provide a review of the literature of this condition.

Summary of background data: Primary lymphoma of the cauda equina is extremely rare, and has been reported in 8 cases previously. This report is the first to describe a case of primary nasal type NK/T-cell lymphoma of the cauda equina.

Methods: We report the case of a 67-year-old man presenting the symptoms of cauda equina syndrome caused by primary lymphoma of the cauda equina.

Results: After laminectomy and removal of the tumor, the patient recovered from the symptoms of cauda equina syndrome except for bladder and bowel dysfunction. Further investigations including immunohistochemical stains made a diagnosis of primary nasal type NK/T-cell lymphoma of the cauda equina, and the patient received radiotherapy to the lumbosacral area. Brain metastasis was detected 8 months after surgery, and the patient died 14 months after his initial clinical presentation despite additional treatments including whole-brain radiotherapy and oral chemotherapy.

Conclusion: Although primary lymphoma of the cauda equina is extremely rare, the prognosis of this condition is thought to be poor. Early definitive diagnosis with examination of the cerebrospinal fluid followed by combined treatment with radiotherapy and high-dose methotrexate should be considered.

PubMed Disclaimer

Similar articles

Cited by

MeSH terms

LinkOut - more resources