2022
DOI: 10.2152/jmi.69.312
|View full text |Cite
|
Sign up to set email alerts
|

Hemangioblastoma of the Cauda Equina : A Case Report and Review of the Literature

Abstract: Introduction : Hemangioblastoma in the spine mainly occurs at the cervical and thoracic levels and is often associated with von Hippel-Lindau (VHL) syndrome. Here, we reported a quite rare case of spinal sporadic hemangioblastoma arising from the cauda equina. Case presentation : A 66-year-old woman presented with a 5-year history of low back and leg pain. Imaging revealed a hypervascular intradural extramedullary tumor in the lumbar region. Preoperative angiography helped to identify the feeding arteries and … Show more

Help me understand this report

Search citation statements

Order By: Relevance

Paper Sections

Select...
1

Citation Types

0
2
0

Year Published

2023
2023
2024
2024

Publication Types

Select...
5

Relationship

0
5

Authors

Journals

citations
Cited by 5 publications
(2 citation statements)
references
References 16 publications
0
2
0
Order By: Relevance
“…Radiological findings of MRI in the form of T1 hyperintense lesions was reported in both brain T.B [6] and EHE [7]. A recent report of a case of spinal hemangioendothelioma which was initially misdiagnosed as a spinal TB by the diagnostic MRI ultimately , tissue diagnosis was the only way to reach the accurate diagnosis in this complicated case [8]. Lienalidomide has been reported to have a good disease control even with CNS EHE [9].…”
Section: Discussionmentioning
confidence: 98%
“…Radiological findings of MRI in the form of T1 hyperintense lesions was reported in both brain T.B [6] and EHE [7]. A recent report of a case of spinal hemangioendothelioma which was initially misdiagnosed as a spinal TB by the diagnostic MRI ultimately , tissue diagnosis was the only way to reach the accurate diagnosis in this complicated case [8]. Lienalidomide has been reported to have a good disease control even with CNS EHE [9].…”
Section: Discussionmentioning
confidence: 98%
“…Among all these cases, only a few cases are identified as isolated hemangioblastomas of filum terminale. [4][5][6][7][8][9][10][11][12] In this report, we present a rare case of hemangioblastoma of filum terminale not associated with von Hippel -Lindau syndrome.…”
mentioning
confidence: 99%