Zhurnal voprosy neirokhirurgii imeni N. N. Burdenko · 2026
[Extradural angiolipoma of the thoracic spine: a case report and literature review].
СтатьяКлинический случайОбзорАннотация на английскомНазвание и аннотация: Перевод в очереди
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Shmelev N D, Konovalov N A, Brinyuk E S, Kaprovoi S V, Onoprienko R A, Zakirov B A, Gabrielyan L R, Kuzmina K V
Аннотация
BACKGROUND: Spinal angiolipomas (SA) are rare primary tumors accounting for 0.14-1.2% of all spinal cord and spine tumors and approximately 3% of extradural spinal neoplasms (<0.1% of all primary CNS tumors). Histologically, SA consists of mature adipocytes and abnormally developed vessels. Clinical presentation of this tumor is due to severe spinal cord compression.
MATERIAL AND METHODS: The authors present a 33-year-old patient with severe spinal cord compression who underwent resection of Th6-Th8 spinal angiolipoma. The Pubmed, Medline, EMBASE, Cochrane Library and eLibrary databases were screened using appropriate keywords.
RESULTS AND DISCUSSION: Extradural tumor > 5 cm causing severe dural sac compression was excised. In early postoperative period, there were complete regression of preoperative lower spastic paraparesis and gait improvement.
CONCLUSION: SAs are extremely rare, and their total resection with preservation or improvement of neurological status is possible in a specialized hospital.
MATERIAL AND METHODS: The authors present a 33-year-old patient with severe spinal cord compression who underwent resection of Th6-Th8 spinal angiolipoma. The Pubmed, Medline, EMBASE, Cochrane Library and eLibrary databases were screened using appropriate keywords.
RESULTS AND DISCUSSION: Extradural tumor > 5 cm causing severe dural sac compression was excised. In early postoperative period, there were complete regression of preoperative lower spastic paraparesis and gait improvement.
CONCLUSION: SAs are extremely rare, and their total resection with preservation or improvement of neurological status is possible in a specialized hospital.