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表现为全脊髓空洞症的背侧血管母细胞瘤。

Dorsal hemangioblastoma manifesting as holocord syringomyelia.

作者信息

Dutta Gautam, Singh Daljit, Singh Hukum, Srivastava Arvind K, Jagetia Anita, Agrawal Atul

机构信息

Department of Neuro-Surgery, Govind Ballav Pant Institute of Postgraduate Medical Education and Research (GIPMER), New Delhi, India.

出版信息

Surg Neurol Int. 2018 Apr 5;9:73. doi: 10.4103/sni.sni_47_18. eCollection 2018.

DOI:10.4103/sni.sni_47_18
PMID:29721352
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC5909086/
Abstract

BACKGROUND

Intramedullary spinal hemangioblastomas are known to be accompanied by syringomyelia.

CASE DESCRIPTION

Here, we report a patient who presented with symptoms of a Chiari malformation but was found to have a D4 intramedullary hemangioblastoma with a holocord syrinx.

CONCLUSIONS

Although rare, neurosurgeons should keep in mind the possibility of an intramedullary hemangioblastoma in patients presenting with symptoms of a Chiari malformation.

摘要

背景

已知髓内脊髓血管母细胞瘤伴有脊髓空洞症。

病例描述

在此，我们报告一名表现为Chiari畸形症状的患者，但发现其患有D4节段髓内血管母细胞瘤并伴有全脊髓空洞症。

结论

尽管罕见，但神经外科医生应牢记，表现为Chiari畸形症状的患者存在髓内血管母细胞瘤的可能性。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/5909086/79fd48479dc2/SNI-9-73-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/5909086/f7acbf3f1220/SNI-9-73-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/5909086/79fd48479dc2/SNI-9-73-g002.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/5909086/f7acbf3f1220/SNI-9-73-g001.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/d9ed/5909086/79fd48479dc2/SNI-9-73-g002.jpg

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本文引用的文献

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J Neurol Neurosurg Psychiatry. 2007 Feb;78(2):146. doi: 10.1136/jnnp.2006.099440.
2
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J Chin Med Assoc. 2005 Jan;68(1):40-4. doi: 10.1016/S1726-4901(09)70131-5.
3
Secondary holocord syringomyelia with spinal hemangioblastoma: a report of two cases.继发性全脊髓空洞症合并脊髓血管母细胞瘤：2例报告
J Neurosurg Case Lessons. 2021 Sep 13;2(11):CASE21296. doi: 10.3171/CASE21296.
Neurol India. 2003 Mar;51(1):67-8.