Calcifying Pseudoneoplasm of the Neuraxis: A Case Illustrating Natural History over 17 Years of Radiologic Surveillance

被引：20

作者：

Barber, Sean M. ^{[1
]}

Low, Jacob Chen Ming ^{[1
]}

Johns, Paul ^{[2
]}

Rich, Philip ^{[3
]}

MacDonald, Bridget ^{[4
]}

Jones, Timothy L. ^{[1
]}

机构：

[1] St George Hosp, Dept Neurosurg, London, England

[2] St George Hosp, Dept Neuropathol, London, England

[3] St George Hosp, Dept Neuroradiol, London, England

[4] Croydon Univ Hosp, Dept Neurol, London, England

来源：

WORLD NEUROSURGERY | 2018年 / 115卷

关键词：

Brain mass; Calcifying pseudoneoplasm of the neuraxis; Epilepsy; Seizure; OF-THE-LITERATURE; CENTRAL-NERVOUS-SYSTEM; FIBRO-OSSEOUS LESION; FIBROOSSEOUS LESION; CORPUS-CALLOSUM; POSTERIOR-FOSSA; FORAMEN MAGNUM; SKULL BASE; PSEUDOTUMOR; SPINE;

D O I：

10.1016/j.wneu.2018.04.175

中图分类号：

R74 [神经病学与精神病学];

学科分类号：

摘要：

BACKGROUND: Calcifying pseudoneoplasm of the neuraxis (CAPNON) is a rare central nervous system lesion that can occur in both the brain and the spine. Although this entity is poorly understood, radiologic and histological features have been identified. CASE DESCRIPTION: We report a unique case of a 31-year-old patient who was managed with antiepileptic medication for 17 years before requiring neurosurgical intervention for tumor progression. T2-weighted magnetic resonance imaging revealed hyperintensity within the tumor with extensive associated vasogenic edema, which is not normally associated with CAPNON. Resection was successful with no complications. CONCLUSIONS: The present case illustrates the long-term natural history of CAPNON before resection and highlights the variations in radiologic appearance that may be associated with this poorly understood entity.

引用

页码：309 / 319

页数：11

共 63 条

[61] Calcifying Pseudoneoplasm of the Neuraxis Arising From the Sacral Canal: Case Report and Review of the Literature [J].