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髓内海绵状血管畸形:一例报告。

Intramedullary cavernous malformation: A case report.

作者信息

Lucarelli Nicola Maria, Troise Francesca, Antonicelli Valentina, Greco Sara, Morelli Chiara, Maggialetti Nicola

机构信息

Interdisciplinary Department of Medicine, Section of Radiology and Radiation Oncology, University of Bari "Aldo Moro", Bari 70124, Italy.

出版信息

Radiol Case Rep. 2024 Aug 31;19(11):5389-5392. doi: 10.1016/j.radcr.2024.08.001. eCollection 2024 Nov.

DOI:10.1016/j.radcr.2024.08.001
PMID:39285957
原文链接:https://pmc.ncbi.nlm.nih.gov/articles/PMC11402540/
Abstract

Cavernous malformations are rare vascular anomalies of the central nervous system, occurring in the spinal cord in just 5% of cases. Despite being documented in the literature, intramedullary cavernous malformations are exceedingly rare and often challenging to distinguish from other intramedullary lesions. We report a case of a 42-year-old patient with back pain, right-sided dysesthesias, and impaired proprioception in the distal limbs for approximately 3 months. Magnetic resonance imaging, crucial for differential diagnosis, identified intramedullary cavernous malformations at T11-12. Several conditions can hide the real cause of back pain; however, magnetic resonance imaging can reveal common conditions (such as discal hernia) and rare findings like cavernous malformations. Magnetic resonance imaging remains the study of choice for diagnosing and characterizing intramedullary cavernous malformations.

摘要

海绵状血管畸形是中枢神经系统罕见的血管异常,仅5%的病例发生在脊髓。尽管文献中有记载,但髓内海绵状血管畸形极为罕见,且常常难以与其他髓内病变相区分。我们报告一例42岁患者,有背痛、右侧感觉异常以及远端肢体本体感觉受损约3个月。磁共振成像对于鉴别诊断至关重要,其显示在T11 - 12水平存在髓内海绵状血管畸形。有几种情况可能掩盖背痛的真正病因;然而,磁共振成像能够揭示常见情况(如椎间盘突出)以及像海绵状血管畸形这样的罕见发现。磁共振成像仍然是诊断和表征髓内海绵状血管畸形的首选检查方法。

https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18c/11402540/d34ad7b97e53/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18c/11402540/88b98f6b033c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18c/11402540/f4eea536006f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18c/11402540/d34ad7b97e53/gr3.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18c/11402540/88b98f6b033c/gr1.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18c/11402540/f4eea536006f/gr2.jpg
https://cdn.ncbi.nlm.nih.gov/pmc/blobs/a18c/11402540/d34ad7b97e53/gr3.jpg

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本文引用的文献

1
Intramedullary spinal cavernous malformations with high ossification: a case report and review of the literature.伴有高度骨化的脊髓髓内海绵状血管畸形:一例报告并文献复习
Chin Neurosurg J. 2023 Apr 19;9(1):11. doi: 10.1186/s41016-023-00323-6.
2
Functional neurological outcome of spinal cavernous malformation surgery.脊髓海绵状血管畸形手术的功能神经预后。
Eur Spine J. 2023 May;32(5):1714-1720. doi: 10.1007/s00586-023-07640-5. Epub 2023 Mar 16.
3
Multiple spinal intramedullary cavernous angiomas with bleeding episode mimicking an intramedullary tumor.
多发脊髓髓内海绵状血管畸形伴出血发作,类似于髓内肿瘤。
J Radiol Case Rep. 2022 Mar 1;16(3):15-22. doi: 10.3941/jrcr.v16i3.4251. eCollection 2022 Mar.
4
Natural course of untreated spinal cord cavernous malformations: a follow-up study within the initial 5 years after diagnosis.未经治疗的脊髓海绵状血管畸形的自然病程:诊断后最初5年内的随访研究
J Neurosurg Spine. 2021 Dec 17;36(6):1030-1034. doi: 10.3171/2021.9.SPINE211052. Print 2022 Jun 1.
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[Spinal cord vascular diseases].[脊髓血管疾病]
Radiologe. 2021 Mar;61(3):258-262. doi: 10.1007/s00117-021-00828-0. Epub 2021 Feb 18.
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Radiation-induced brain cavernomas in elderly: review of the literature and a rare case report.老年人群中辐射诱发的脑海绵状血管瘤:文献综述及一例罕见病例报告
Acta Biomed. 2019 Apr 24;90(5-S):77-83. doi: 10.23750/abm.v90i5-S.8328.
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Varying clinical presentations of familial cerebral cavernous malformations (CCMs) and spinal cord cavernous malformations (SCCMs).家族性脑海绵状血管畸形(CCM)和脊髓海绵状血管畸形(SCCM)的不同临床表现。
Radiol Case Rep. 2015 Dec 7;7(3):678. doi: 10.2484/rcr.v7i3.678. eCollection 2012.
8
Cavernoma of the conus medullaris mimicking transverse myelitis.圆锥部海绵状血管瘤误诊为横贯性脊髓炎。
Singapore Med J. 2013 Feb;54(2):e24-7. doi: 10.11622/smedj.2013034.